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ORIGINAL RESEARCH article

Front. Nutr., 16 July 2024
Sec. Nutritional Epidemiology
This article is part of the Research Topic Influence of Dietary Factors, Nutrients, and the Gut-Lung Axis on Respiratory Health View all 10 articles

Association between nutrition-related indicators with the risk of chronic obstructive pulmonary disease and all-cause mortality in the elderly population: evidence from NHANES

  • 1School of Clinical Medicine, Jiangxi University of Chinese Medicine, Nanchang, Jiangxi, China
  • 2Affiliated Hospital of Jiangxi University of Traditional Chinese Medicine, Nanchang, Jiangxi, China

Background: This study aims to use six nutrition-related indicators to assess the relationship between nutritional status and the risk of COPD as well as the all-cause mortality rate, and to determine the most reliable predictive indicators.

Methods: Data from the National Health and Nutrition Examination Survey (NHANES) spanning the years 2013 to 2018 were extracted. Nutritional status was evaluated using Controlling nutritional status (CONUT) score, Geriatric Nutritional Risk Index (GNRI), Advanced Lung Cancer Inflammation Index (ALI), Prognostic Nutritional Index (PNI), Triglycerides (TG) × Total Cholesterol (TC) × Body Weight (BW) Index (TCBI), and Albumin-to-Globulin Ratio (AGR) nutritional-related indicators. Multivariate weighted logistic and Cox regression models were employed to assess the correlation between the six nutritional-related indicators and the risk of COPD and as all-cause mortality. The restricted cubic spline tests were applied to explore potential nonlinear relationships, and ROC curves and C-index analyses were conducted to compare the predictive capabilities of different indicators. Stratified analysis and propensity score matching (PSM) to assess the robustness of the results.

Results: In this study, Lower ALI, lower GNRI, and higher CONUT scores were positively correlated with an increased risk of COPD (OR: 1.77, 95% CI: 1.10–2.84) (OR: 8.66, 95% CI: 2.95–25.5), and (OR: 5.11, 95% CI: 1.72–15.2), respectively. It was found that ALI and GNRI had a non-linear relationship with the risk of COPD. After propensity score matching (PSM), the associations between ALI, GNRI, CONUT scores, and COPD remained consistent. Lower ALI, PNI, and GNRI scores were positively associated with all-cause mortality in COPD patients (HR: 2.41, 95% CI: 1.10–5.27), (HR: 3.76, 95% CI: 1.89–7.48), and (HR: 4.55, 95% CI: 1.30–15.9), respectively, with GNRI displaying a non-linear relationship with all-cause mortality. ROC curve and C-index analyses indicated that ALI had the best predictive ability for both COPD risk and all-cause mortality.

Conclusion: ALI, GNRI, and CONUT scores are correlated with the risk of COPD, while ALI, PNI, and GNRI scores are associated with all-cause mortality in COPD patients. Compared to other nutritional scores, ALI may provide more effective predictive value for both risk and all-cause mortality.

Introduction

Chronic obstructive pulmonary disease (COPD) is one of the most common respiratory system diseases and has become the third leading cause of death globally. It is characterized by persistent and usually progressive airflow limitation, which is caused by abnormalities in the airways and/or alveoli, leading to chronic respiratory symptoms such as difficulty breathing, coughing, and sputum production (1). There are reports indicating that COPD is more common in the elderly population, with the incidence rate in individuals aged 60 and above being nearly four times higher than that in individuals below 60 (2). Malnutrition is closely associated with the occurrence of COPD in the elderly population (3, 4), and it can increase the risk of exacerbations in COPD, affecting the prognosis of COPD patients, including poor exercise tolerance, increased risk of hospitalization, severe airflow obstruction, or even death (5, 6). Therefore, nutritional status assessment should be widely incorporated into the screening and management of COPD in the elderly.

The European Society for Clinical Nutrition and Metabolic Care (ESPEN) consensus statement in 2017 has long emphasized the use of easily accessible and simple nutritional screening tools in clinical settings to identify patients at risk of malnutrition (7). Several new laboratory-based nutritional indicators have emerged in recent years, including the Controlling Nutritional Status (CONUT) Score (8), Advanced Lung Cancer Inflammation Index (ALI) (9), Geriatric Nutritional Risk Index (GNRI) (10), Prognostic Nutritional Index (PNI) (11), Triglycerides (TG) × Total Cholesterol (TC) × Body Weight (BW) Index (TCBI) (12), and Albumin-to-Globulin Ratio (AGR) (13). CONUT has been used as an indicator for assessing the risk of mortality in patients with rheumatoid arthritis and type 2 diabetes (14, 15). ALI has been used to predict the prognosis of hypertension and heart failure (16, 17). GNRI, TCBI, PNI and AGR have also shown good characteristics in predicting disease risk and prognosis (1821).

Previous evidence suggests that malnutrition is associated with the development of COPD (3, 22), but the inflammatory processes, oxidative stress, and immune function cannot be overlooked (23, 24). The regulation of nutritional status is based on inflammatory and oxidative stress processes, both of which are interconnected with the immune system (25). For instance, malnourished COPD patients are more susceptible to the effects of inflammation and oxidative stress (26), and weight loss commonly observed in patients with COPD may be related to inflammation. Certain pro-inflammatory cytokines interacting with glucagon-like peptide-1 (GLP-1) released from intestinal tissues may lead to unintended weight loss (27). Nutritional indicators such as the CONUT, composed of lymphocyte count, albumin, and TC, and the PNI, composed of lymphocyte count and albumin, not only assess nutritional status but also involve immune status. Lymphocytes primarily mediate adaptive immunity, playing a regulatory or protective role, and low lymphocyte count often indicates poor immune status, while albumin levels typically reflect nutritional status (28, 29). The ALI, consisting of body mass index (BMI), albumin, and neutrophil to lymphocyte ratio (NLR), addresses both nutritional and inflammatory conditions. Previous studies have shown that the NLR within ALI can serve as a systemic inflammatory marker for the risk of COPD (30). Additionally, the GNRI, related to albumin levels and weight, the TCBI combining triglycerides, total cholesterol, and body weight, and the AGR, composed of albumin and globulin, primarily assess nutritional status. Previous studies have often focused on single inflammation assessments in COPD (31, 32), and there is a lack of research focusing on the relationship between nutritional status assessment and the risk and prognosis of COPD.

This study, based on the National Health and Nutrition Examination Survey (NHANES) database, aims to assess the associations between six nutrition-related indicators and the risk of COPD as well as the all-cause mortality in the elderly population in the United States. Furthermore, we endeavor to identify the optimal predictive indicators in this context.

Materials and methods

Study population

NHANES, led by the Centers for Disease Control and Prevention, employs a complex, multistage probability sampling design. It is a nationally representative survey aimed at assessing the health and nutritional status of adults and children in the United States. The survey encompasses demographic, dietary, examination, laboratory, and questionnaire data. The NHANES research protocol has received approval from the National Center for Health Statistics Research Ethics Review Board, and written informed consent has been obtained from all participants.

For this cross-sectional analysis, we selected data from 2013 to 2018 as the basis for our analysis, as clear answers regarding the definition of COPD were only available during this period, covering a total of 29,400 individuals. Firstly, since we are focusing on the elderly population in the United States, we excluded individuals under the age of 65. Additionally, considering the complex sampling design and sample weights of NHANES, we removed missing values. (1) Individuals who did not clearly answer whether they had COPD or had missing self-data were excluded. (2) Individuals lacking data on variables such as albumin, globulin, TC, TG, BW, BMI, neutrophil count, or lymphocyte count, which are crucial for calculating nutritional indicators, were excluded. (3) Data missing from covariates were also excluded. In the end, a total of 3,180 individuals met the inclusion criteria for this study (Figure 1).

Figure 1
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Figure 1. Flowchart for the selection of eligible participants.

Exposure variable

The specific calculation methods for each indicator are detailed in Table 1. Levels of albumin, globulin, TC, and TG were measured using the Roche Cobas 6,000 (c501 module) analyzer. Whole blood cell counts were conducted on blood specimens using an automated hematology analyzer (Coulter DxH 800 analyzer), providing blood cell distribution for all participants, including lymphocyte and neutrophil counts. Height and weight were measured during examinations at the Mobile Examination Center (MEC). Nutrition-related indicators ALI, PNI, TCBI, and AGR were categorized into three groups based on tertiles (T1, T2, and T3 corresponding to the first, second, and third tertiles). Based on CONUT scores, the severity of malnutrition was defined in three groups: normal (0–1), mild to moderate (2–8), and severe (9–12) (8). Three levels of nutrition-related risk were defined based on GNRI levels: no risk (GNRI >98), low to moderate risk (GNRI: 82 to ≤98), and major risk (GNRI <82) (10).

Table 1
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Table 1. Details of the nutritional indices utilized in the study.

Outcome variable

The definition of COPD is a positive response to the question: “Has a doctor or other health professional ever told you that you have COPD?” When participants answered “yes,” we considered them to have COPD. Previous research utilizing NHANES data has indicated that self-reported COPD diagnosis is an effective method (3335).

Identification of mortality

To assess the impact of nutrition-related indicators on overall mortality in COPD patients, we further conducted a cohort analysis. All-cause mortality was determined using death data recorded by the National Death Index (NDI) as of December 31, 2019. These records can be linked to NHANES data, and death files are available online at https://www.cdc.gov/nchs/data-linkage/mortality.htm. The definition of causes of death is based on the International Classification of Diseases, 10th Revision (ICD-10).

Covariates definition

Covariates in this study include age, gender, race, education level, marital status, BMI, poverty income ratio (PIR), smoking status, hypertension, diabetes, cardiovascular disease (CVD), and hyperlipidemia. BMI is categorized as Normal (<25 Kg/m2), Overweight (≥25, <30 Kg/m2), and Obese (≥30 Kg/m2). PIR is divided into three groups: Low (≤1.39), Medium (>1.39, ≤3.49), and High (>3.49). Smoking status is categorized as current, former, or never smoking. Current smokers are individuals who have smoked over 100 cigarettes and currently smoke occasionally or continuously. Former smokers are individuals who have smoked over 100 cigarettes but are not currently smoking. Never smokers are individuals who have smoked fewer than 100 cigarettes in their lifetime. For CVD, a positive response to whether a doctor or other health professional has ever told you that you have congestive heart failure/coronary heart disease/angina/heart attack/stroke was defined as having CVD. Hyperlipidemia is defined as HDL ≤ 40 mg/dL in males and ≤50 mg/dL in females, or triglycerides ≥150 mg/dL, or total cholesterol ≥200 mg/dL, or low-density lipoprotein ≥130 mg/dL. Additionally, individuals reporting the use of cholesterol-lowering medication were also classified as having hyperlipidemia. We obtained the average blood pressure from three consecutive measurements taken at rest. Hypertension was defined as self-reported hypertension, or average systolic blood pressure ≥ 140 mmHg, or average diastolic blood pressure ≥ 90 mmHg, or the use of antihypertensive medication. Diabetes was defined as self-reported diagnosis of diabetes, or fasting blood glucose ≥7.0 mmol/L, or 2-h oral glucose tolerance level/random blood glucose ≥11.1 mmol/L, or glycated hemoglobin (HbA1c) ≥6.5 mmol/L, or the use of antidiabetic medication.

Statistical analyses

Participants’ characteristics were reported as mean ± standard deviation (SD) for continuous variables and as percentages for categorical variables. Participants were divided into two groups based on whether they had COPD. The weighted t-test was used to assess differences in continuous variables between COPD and non-COPD participants, while the weighted chi-square test was used to evaluate differences in categorical variables.

In cross-sectional study analysis, weighted multivariable logistic regression analysis was conducted to assess the association between six nutrition-related indicators and COPD risk. The results were presented as odds ratios (ORs) with 95% confidence intervals (CIs). Logistic regression models were evaluated by gradually adjusting covariates: the crude model was unadjusted, model 1 adjusted for age, gender, and race, model 2 further adjusted for PIR, BMI, education level, and smoking status, and model 3 additionally adjusted for cardiovascular disease, hypertension, diabetes, and hyperlipidemia. To explore the potential nonlinear associations between nutrition-related indicators and the risk of COPD, restricted cubic splines (RCS) were further fitted. Three knots were set at the 10th, 50th, and 90th percentiles, with the 50th percentile as the reference.

In the cohort study analysis, we evaluated the relationship between six nutrition-related indicators and the overall survival of COPD patients using Kaplan–Meier (KM) curves. The analysis was conducted using a two-sided log-rank test. Additionally, weighted multivariable Cox regression analysis was performed to assess the correlation between the six nutrition-related indicators and the all-cause mortality of COPD patients. The results were presented as hazard ratios (HRs) and 95% confidence intervals (CIs). The same adjustments for covariates were applied to evaluate the Cox regression model and explore potential nonlinear associations between nutrition-related indicators and the risk of all-cause mortality in COPD patients.

Finally, the predictive value of nutrition-related indicators for assessing the risk of COPD and all-cause mortality was compared using the receiver operating characteristic (ROC) curve and the C-index. The best predictive indicators were determined. Stratified analysis was performed based on gender (male or female), smoking status (non-smoker or smoker), cardiovascular disease (yes or no), diabetes (yes or no), hypertension (yes or no), and hyperlipidemia (yes or no) to explore the interactions between these factors and the best predictive indicators. In addition, to further validate the association between nutrition-related indicators and the risk of COPD, a sensitivity analysis was conducted using a 1:2 nearest neighbor propensity score matching (PSM) method to balance the case and control groups, including age, gender, race, PIR, smoking status, education level, CVD, and diabetes as confounding factors for matching. Statistical analysis was performed using R Studio (version 4.2.2) and involved R packages such as “survey,” “survival,” “survminer,” “rms,” “ggplot2,” “pROC,” “MatchIt,” and “jskm.” The significance level was set at p < 0.05 (two-tailed).

Results

General characteristics of the study population

The study involved a total of 3,180 participants (mean [SE] age of 72.6 [5.3] years), including 272 diagnosed with COPD (171 males [weighted proportion 56%], 101 females [weighted proportion 44%]). Compared to the non-COPD group, COPD patients had a higher proportion of non-Hispanic White individuals (196 [86%] vs. 1,454 [79%]), a higher percentage of smokers (74 [25%] vs. 240 [7.0%]), lower education levels (College Graduate or above) (34 [19%] vs. 673 [32%]), and were more likely to have comorbidities such as CVD (147 [53%] vs. 747 [24%]) and diabetes (115 [42%] vs. 1,050 [29%]). Additionally, there were statistically significant differences between the two groups in terms of poverty level and age (all p-values <0.05) (Table 2).

Table 2
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Table 2. Baseline characteristics of study participants by incident COPD.

Association between nutrition-related indicators with the risk of COPD

Based on a weighted logistic regression model, we assessed the relationship between six nutrition-related indicators and the risk of COPD. In the fully adjusted model (Model 3), the results revealed a significant association between an elevated CONUT score (9–13) (OR: 5.11, 95% CI: 1.72–15.2), lower GNRI score (<82) (OR: 8.66, 95% CI: 2.95–25.5), and lower ALI score (T1: ≤43.88) (OR: 1.77, 95% CI: 1.10–2.84) with an increased risk of COPD (Table 3).

Table 3
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Table 3. Association of Nutrition-Related Indicators with the risk of COPD using weighted logistic analysis.

Association between nutrition-related indicators and all-cause mortality in COPD patients

In the cohort study, the median follow-up time was 33 months. Among 271 COPD patients, there were 79 cases (29.2%) of all-cause mortality. The KM curve demonstrated the incidence of all-cause mortality in the COPD patient population (Figure 2), showing that COPD patients with lower PNI, GNRI, and ALI indices experienced poorer overall survival.

Figure 2
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Figure 2. Compute Kaplan–Meier curves for all-cause mortality categorized by ALI (A), PNI (B), GNRI (C), CONUT (D), TCBI (E), and AGR (F). ALI, Advanced Lung Cancer Inflammation Index; PNI, Prognostic Nutritional Index; GNRI, Geriatric Nutritional Risk Index; CONUT score, Controlling Nutritional Status score; TCBI, Triglycerides × Total Cholesterol × Body Weight Index; AGR, Albumin-to-Globulin Ratio.

We used a weighted Cox regression model to evaluate the relationship between nutrition-related indicators and all-cause mortality in COPD patients. The results of Model 3 showed a significant association between PNI, GNRI, ALI, TCBI, and all-cause mortality in COPD patients. Specifically, compared to the highest quartile (T3), the lowest quartile (T1) of PNI and ALI was associated with increased risk of all-cause mortality in COPD patients (HR: 3.76, 95% CI: 1.89–7.48), (HR: 2.41, 95% CI: 1.10–5.27) (Table 4). On the other hand, compared to the high GNRI, the low GNRI was associated with increased risk of all-cause mortality in COPD patients (HR: 4.55, 95% CI: 1.30–15.9). Furthermore, compared to the highest quartile, the second quartile of TCBI was associated with increased risk of all-cause mortality in COPD patients (Table 4).

Table 4
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Table 4. Association of Nutrition-Related Indicators with all-cause mortality in COPD patients was investigated using weighted Cox regression analysis.

Nonlinear relationship assessment

To further explore the nonlinear associations between nutritional-related indicators (treated as continuous variables) and the risk of COPD and all-cause mortality, we employed RCS with weighting. Based on the multivariate regression model (Model 3), RCS analysis revealed a nonlinear association between ALI and GNRI with the risk of COPD (p for nonlinear <0.05), while a linear association was observed between CONUT and the risk of COPD (p for nonlinear = 0.51) (Figure 3A). For all-cause mortality rates, the results indicated a nonlinear association between GNRI and the all-cause mortality of COPD patients (p for nonlinear <0.05), while no such nonlinear association was observed for ALI and PNI (Figure 3B).

Figure 3
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Figure 3. Nonlinear tests for nutritional-related indicators regarding COPD risk and all-cause mortality. (A) Nonlinear tests between ALI, GNRI, and CONUT (from left to right) and COPD risk. (B) Nonlinear tests between ALI, PNI, and GNRI (from left to right) and all-cause mortality among COPD patients. ALI, Advanced Lung Cancer Inflammation Index; PNI, Prognostic Nutritional Index; GNRI, Geriatric Nutritional Risk Index; CONUT score, Controlling Nutritional Status score; OR, odds ratio; HR, hazard ratio.

Comparison of nutritional-related indicators in predicting disease risk and all-cause mortality

We compared the ability of nutritional-related indicators to predict disease risk and all-cause mortality based on the ROC curves and C-index derived from the crude model. In assessing COPD incidence risk, ALI outperformed GNRI and CONUT, with the highest area under the ROC curve (AUC) value (ALI: 0.601 vs. CONUT: 0.582 vs. GNRI: 0.528) (Figure 4A) and the highest C-index (ALI: 0.601 vs. CONUT: 0.582 vs. GNRI: 0.529) (Supplementary Table S1). For all-cause mortality assessment, ALI exhibited the highest AUC value compared to PNI and GNRI (ALI: 0.587 vs. PNI: 0.559 vs. GNRI: 0.533) (Figure 4B), and a relatively higher C-index (ALI: 0.642 vs. PNI: 0.648 vs. GNRI: 0.522) (Supplementary Table S2). Similar results were observed across other models (Model 1 to Model 3). Therefore, we consider ALI to be the optimal indicator for predicting the risk of COPD incidence and all-cause mortality among COPD patients in this study.

Figure 4
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Figure 4. ROC curves for predicting COPD risk and all-cause mortality. (A) ROC curves for predicting COPD risk by ALI, CONUT, and GNRI (from left to right). (B) ROC curves for predicting all-cause mortality among COPD patients by ALI, PNI, and GNRI (from left to right). ALI, Advanced Lung Cancer Inflammation Index; PNI, Prognostic Nutritional Index; GNRI, Geriatric Nutritional Risk Index; CONUT score, Controlling Nutritional Status score.

Subgroup and sensitivity analysis

Overall, ALI is considered the optimal indicator for predicting the incidence risk and all-cause mortality of COPD. Subgroup analyses stratified by gender, smoking status, CVD, diabetes, hypertension, and hyperlipidemia revealed that, compared to the highest tertile (T3), the lowest tertile (T1) of ALI exhibited a stronger correlation with COPD risk and all-cause mortality in females, individuals with hyperlipidemia, and those without hypertension (Supplementary Tables S3, S4). Additionally, no significant interactions were observed between ALI levels and the stratified variables, with all interaction p-values exceeding 0.05.

After using the nearest neighbor PSM to establish a control group, the relationship between six nutrition-related indicators and the risk of COPD was analyzed again. After PSM, the dataset included 564 participants in the non-COPD group and 263 participants in the COPD group, with no statistically significant differences in covariates (Supplementary Table S5). Logistic regression analysis after matching showed that in the fully adjusted model, compared to high ALI, low ALI was significantly associated with an increased risk of COPD (OR: 1.77, 95% CI: 1.10–2.84), while CONUT score and GNRI score also remained consistent with the results of the logistic regression before matching (Supplementary Table S6).

Discussion

This study investigated the relationships between six nutrition-related indicators, including GNRI, ALI, TCBI, PNI, CONUT, and AGR, and the risk of COPD incidence and all-cause mortality in a nationally representative sample of the elderly population in the United States. We compared the performance of these indicators for the first time in predicting COPD risk and all-cause mortality. We found that malnutrition in the elderly population was significantly associated with a higher risk of COPD incidence and all-cause mortality, with ALI, GNRI, and CONUT being correlated with COPD risk, and ALI, GNRI, and PNI being associated with all-cause mortality among COPD patients. Additionally, we observed nonlinear relationships between ALI, GNRI, and COPD risk, as well as between GNRI and all-cause mortality. Furthermore, compared to other nutrition-related indicators, ALI emerged as the top predictor for assessing both COPD risk and all-cause mortality in the elderly population.

From an overall perspective, poor nutritional status has an impact on the risk of developing COPD and all-cause mortality rate. Firstly, previous reports have clearly indicated that inflammation and oxidative stress are the core pathological processes of COPD (36). Malnutrition can potentially increase inflammation and oxidative stress (37), and it can also affect the immune system, as immune responses are strongly regulated by oxidative stress and inflammation (38). Consequently, this may further weaken the body’s immune response (25) and increase the risk of developing COPD. Furthermore, studies on the role of nutrients and antioxidants have shown that a high intake of foods rich in antioxidants (such as fresh fruits and vegetables) and antioxidant nutrients (both vitamins and non-vitamins) can effectively enhance antioxidant and anti-inflammatory abilities (39, 40), thus playing a positive role in reducing the incidence of COPD (41, 42). Moreover, for patients with COPD, disease-related malnutrition is a common problem (43). Malnutrition can accelerate the decline in respiratory function, leading to loss of lung tissue and decreased quality and thickness of respiratory-related muscles, such as the diaphragm (44). Additionally, under conditions of malnutrition, respiratory muscles become weak and fatigue earlier, and there is poorer lung diffusion capacity and lower exercise tolerance (45). It is worth noting that malnutrition weakens immune defenses, significantly increasing the risk of lung infections and also being one of the reasons for increased risk of death (22). In summary, poor nutritional status can have a profound impact on the risk of developing COPD and overall health outcomes. Adequate intake of antioxidants and proper nutrition play an important role in maintaining lung health and reducing the risk of COPD.

Previous clinical studies have explored the associations of GNRI, ALI, TCBI, PNI, CONUT, and AGR with various disease outcomes, with fewer studies focusing on COPD. Chai X (46) investigated the association between GNRI and all-cause mortality in individuals aged 18 and above, suggesting a correlation between malnutrition and higher all-cause mortality in COPD. Suzuki E et al. (47) demonstrated that PNI could serve as a potential predictor for exacerbation in elderly subjects with COPD. Additionally, studies have indicated that CONUT scores have prognostic value for frequent exacerbations in elderly COPD patients (48). Our findings align with previous research, but we also reveal that GNRI is not only associated with all-cause mortality in COPD but also with the risk of COPD incidence in the elderly population, with these relationships being nonlinear. A recent study in the general United States population suggested that, compared to other nutritional scores (TCBI, CONUT, GNRI), PNI might offer superior predictive value for all-cause mortality. However, our study among elderly population presents a different conclusion, highlighting ALI as a novel predictor for COPD risk and all-cause mortality. Through ROC curve and C-index analysis, we found that among the six nutrition-related indicators, ALI exhibited superior predictive efficacy for both COPD risk and all-cause mortality.

ALI, as the best predictive indicator, includes three factors: BMI, serum albumin levels, and the NLR. It is calculated by multiplying BMI by the ratio of serum albumin to the NLR. BMI and serum albumin levels reflect nutritional status (49, 50), while NLR reflects inflammatory status (51), making ALI a comprehensive assessment index based on nutrition and inflammation. BMI is a fundamental measure of body fat content, and the Global Leadership Initiative on Malnutrition (GLIM) diagnostic criteria for malnutrition utilize BMI (49). It is well known that obesity is often associated with increased rates of chronic diseases. However, research suggests that a BMI below 18.5 is a risk factor for COPD (52, 53), while overweight and obesity (BMI ≥ 25 Kg/m2) may decrease the risk of COPD (53, 54), highlighting a paradox (55). According to our research, it appears that there exists an L-shaped non-linear relationship between ALI and the risk of COPD. A moderately higher BMI may correspond to elevated ALI values, suggesting a better nutritional status. Then, serum albumin is a multifunctional plasma protein, accounting for over 50% of total plasma proteins, and it possesses crucial antioxidant properties. In COPD, inflammation is central to its development, with oxidative stress amplifying inflammatory responses (56). Higher albumin levels contribute to improved antioxidant capacity and protect tissues from inflammatory damage (57). A meta-analysis indicates a significant decrease in serum albumin concentration in COPD patients compared to non-COPD controls (58), while a cross-sectional study of a British population suggests that elevated albumin levels help lower the risk of COPD (59). Thus, the level of albumin is closely associated with the occurrence and progression of COPD. Inflammation increases with the severity of COPD (51), and chronic, persistent inflammation often leads to changes in neutrophils, which further mediate the production and release of specific inflammatory mediators (60, 61), ultimately resulting in irreversible airway damage. Due to the combination of different blood cell populations reflected by NLR expression, which can better indicate inflammatory status compared to individual blood cell markers, NLR has been studied in recent years as a systemic marker of inflammation. Multiple studies have also indicated associations between NLR and the risk of COPD, exacerbation severity, and mortality risk (30, 62), and adjusting nutritional status is also of significant importance for effectively reducing inflammation (37). In conclusion, there exists a complex interaction between malnutrition and inflammation. Therefore, these combined factors may be reasons for the potentially superior predictive value of ALI compared to other nutritional-related indicators.

Additionally, our research suggests a more significant relationship between ALI and COPD risk and all-cause mortality rates in females. Several studies in COPD genetics, such as the COPD Gene study, indicate gender-related genetic components in COPD incidence (63). Moreover, research suggests that females are more susceptible to smoking-related lung injuries (64, 65) and experience more severe inflammatory responses (66). Furthermore, studies propose that females exhibit more severe COPD symptoms (67) and have a greater risk of exacerbations (68, 69). However, the specific mechanisms still need further clarification.

Our study has several strengths. Firstly, it is based on a large sample with national representativeness. Secondly, it identifies ALI as associated with COPD risk for the first time and as an independent predictor of all-cause mortality. However, we acknowledge some limitations. Firstly, our study is cross-sectional, precluding causal inferences. Secondly, the population of COPD patients is defined through self-reporting, which may introduce recall bias. Nonetheless, these patients typically have medical histories, and their COPD diagnoses are typically confirmed by healthcare professionals, a method widely used in previous studies to define COPD (3335). Thirdly, despite controlling for demographic indicators, behavioral risk factors, and various chronic diseases in the analysis, the results may still be influenced by unknown confounding factors. Fourthly, the study was conducted on a representative sample from the United States, and the generalization of the study results to other populations may not be direct.

Conclusion

In conclusion, this research, involving a nationally representative sample of the elderly population in the United States, indicates that nutritional-related indicators, including lower ALI, GNRI, and higher CONUT scores, are associated with the risk of COPD. Furthermore, lower ALI, GNRI, and PNI scores are linked to all-cause mortality. Importantly, compared to other indicators, ALI exhibits optimal performance in predicting both COPD risk and all-cause mortality among COPD patients. The assessment of ALI can enhance the identification of COPD and serve as a valuable prognostic marker in clinical practice.

Data availability statement

The original contributions presented in the study are included in the article/Supplementary material, further inquiries can be directed to the corresponding authors.

Ethics statement

We used publicly available data that were obtained with ethical approval from their respective institutional review boards and informed consent from all participants. No administrative permissions were required for accessing the data.

Author contributions

YX: Conceptualization, Methodology, Software, Writing – original draft, Writing – review & editing. ZY: Conceptualization, Methodology, Software, Writing – original draft. KL: Conceptualization, Methodology, Writing – original draft. LL: Conceptualization, Validation, Writing – review & editing. LX: Data curation, Software, Supervision, Writing – review & editing.

Funding

This work is supported by grants from the Natural Science Foundation of Jiangxi Province (Nos. 20212BAB216061, 20212BAG70038), Jiangxi Clinical Medical Research Center of Lung Diseases (Gan ke fa she [2019] No. 44), Jiangxi University of Chinese Medicine Science and Technology Innovation Team Development Program (No. CXTD22011).

Acknowledgments

The authors thank all the participants and researchers who contributed and collected data. Thanks to Zhang Jing (Second Department of Infectious Disease, Shanghai Fifth People’s Hospital, Fudan University) for his work on the NHANES database. His outstanding work, nhanesR package and webpage, makes it easier for us to explore NHANES database.

Conflict of interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Publisher’s note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

Supplementary material

The Supplementary material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fnut.2024.1380791/full#supplementary-material

References

1. Agusti, A, Celli, BR, Criner, GJ, Halpin, D, Anzueto, A, Barnes, P, et al. Global initiative for chronic obstructive lung disease 2023 report: GOLD executive summary. Eur Respir J. (2023) 61:2300239. doi: 10.1183/13993003.00239-2023

Crossref Full Text | Google Scholar

2. Varmaghani, M, Dehghani, M, Heidari, E, Sharifi, F, Moghaddam, SS, and Farzadfar, F. Global prevalence of chronic obstructive pulmonary disease: systematic review and meta-analysis. East Mediterr Health J. (2019) 25:47–57. doi: 10.26719/emhj.18.014

Crossref Full Text | Google Scholar

3. van Iersel, LEJ, Beijers, R, Gosker, HR, and Schols, A. Nutrition as a modifiable factor in the onset and progression of pulmonary function impairment in COPD: a systematic review. Nutr Rev. (2022) 80:1434–44. doi: 10.1093/nutrit/nuab077

PubMed Abstract | Crossref Full Text | Google Scholar

4. Mete, B, Pehlivan, E, Gulbas, G, and Gunen, H. Prevalence of malnutrition in COPD and its relationship with the parameters related to disease severity. Int J Chron Obstruct Pulmon Dis. (2018) 13:3307–12. doi: 10.2147/COPD.S179609

PubMed Abstract | Crossref Full Text | Google Scholar

5. Kaluzniak-Szymanowska, A, Krzyminska-Siemaszko, R, Deskur-Smielecka, E, Lewandowicz, M, Kaczmarek, B, and Wieczorowska-Tobis, K. Malnutrition, sarcopenia, and malnutrition-sarcopenia syndrome in older adults with COPD. Nutrients. (2021) 14:44. doi: 10.3390/nu14010044

Crossref Full Text | Google Scholar

6. Dávalos-Yerovi, V, Marco, E, Sánchez-Rodríguez, D, Duran, X, Meza-Valderrama, D, Rodríguez, DA, et al. Malnutrition according to GLIM criteria is associated with mortality and hospitalizations in rehabilitation patients with stable chronic obstructive pulmonary disease. Nutrients. (2021) 13:369. doi: 10.3390/nu13020369

PubMed Abstract | Crossref Full Text | Google Scholar

7. Cederholm, T, Barazzoni, R, Austin, P, Ballmer, P, Biolo, G, Bischoff, SC, et al. ESPEN guidelines on definitions and terminology of clinical nutrition. Clin Nutr. (2017) 36:49–64. doi: 10.1016/j.clnu.2016.09.004

PubMed Abstract | Crossref Full Text | Google Scholar

8. Ignacio de Ulíbarri, J, González-Madroño, A, de Villar, NG, González, P, González, B, Mancha, A, et al. CONUT: a tool for controlling nutritional status. First validation in a hospital population. Nutr Hosp. (2005) 20:38–45.

PubMed Abstract | Google Scholar

9. Jafri, SH, Shi, R, and Mills, G. Advance lung cancer inflammation index (ALI) at diagnosis is a prognostic marker in patients with metastatic non-small cell lung cancer (NSCLC): a retrospective review. BMC Cancer. (2013) 13:158. doi: 10.1186/1471-2407-13-158

PubMed Abstract | Crossref Full Text | Google Scholar

10. Bouillanne, O, Morineau, G, Dupont, C, Coulombel, I, Vincent, JP, Nicolis, I, et al. Geriatric nutritional risk index: a new index for evaluating at-risk elderly medical patients. Am J Clin Nutr. (2005) 82:777–83. doi: 10.1093/ajcn/82.4.777

PubMed Abstract | Crossref Full Text | Google Scholar

11. Onodera, T, Goseki, N, and Kosaki, G. Prognostic nutritional index in gastrointestinal surgery of malnourished cancer patients. Nihon Geka Gakkai Zasshi. (1984) 85:1001–5.

PubMed Abstract | Google Scholar

12. Doi, S, Iwata, H, Wada, H, Funamizu, T, Shitara, J, Endo, H, et al. A novel and simply calculated nutritional index serves as a useful prognostic indicator in patients with coronary artery disease. Int J Cardiol. (2018) 262:92–8. doi: 10.1016/j.ijcard.2018.02.039

PubMed Abstract | Crossref Full Text | Google Scholar

13. Li, X, Qin, S, Sun, X, Liu, D, Zhang, B, Xiao, G, et al. Prognostic significance of albumin-globulin score in patients with operable non-small-cell lung Cancer. Ann Surg Oncol. (2018) 25:3647–59. doi: 10.1245/s10434-018-6715-z

PubMed Abstract | Crossref Full Text | Google Scholar

14. Tian, P, Xiong, J, Wu, W, Shi, S, Chen, A, Chen, K, et al. Impact of the malnutrition on mortality in rheumatoid arthritis patients: a cohort study from NHANES 1999-2014. Front Nutr. (2022) 9:993061. doi: 10.3389/fnut.2022.993061

PubMed Abstract | Crossref Full Text | Google Scholar

15. Pan, D, Guo, J, Su, Z, Wang, J, Wu, S, Guo, J, et al. Association of the controlling nutritional status score with all-cause mortality and cancer mortality risk in patients with type 2 diabetes: NHANES 1999-2018. Diabetol Metab Syndr. (2023) 15:175. doi: 10.1186/s13098-023-01138-2

PubMed Abstract | Crossref Full Text | Google Scholar

16. Tu, J, Wu, B, Xiu, J, Deng, J, Lin, S, Lu, J, et al. Advanced lung cancer inflammation index is associated with long-term cardiovascular death in hypertensive patients: national health and nutrition examination study, 1999-2018. Front Physiol. (2023) 14:1074672. doi: 10.3389/fphys.2023.1074672

PubMed Abstract | Crossref Full Text | Google Scholar

17. Yuan, X, Huang, B, Wang, R, Tie, H, and Luo, S. The prognostic value of advanced lung cancer inflammation index (ALI) in elderly patients with heart failure. Front Cardiovasc Med. (2022) 9:934551. doi: 10.3389/fcvm.2022.934551

PubMed Abstract | Crossref Full Text | Google Scholar

18. Chen, SC, Yang, YL, Wu, CH, Huang, SS, Chan, WL, Lin, SJ, et al. Association between preoperative nutritional status and clinical outcomes of patients with coronary artery disease undergoing percutaneous coronary intervention. Nutrients. (2020) 12:1295. doi: 10.3390/nu12051295

Crossref Full Text | Google Scholar

19. Chen, QJ, Qu, HJ, Li, DZ, Li, XM, Zhu, JJ, Xiang, Y, et al. Prognostic nutritional index predicts clinical outcome in patients with acute ST-segment elevation myocardial infarction undergoing primary percutaneous coronary intervention. Sci Rep. (2017) 7:3285. doi: 10.1038/s41598-017-03364-x

PubMed Abstract | Crossref Full Text | Google Scholar

20. Liang, L, Zhao, X, Huang, L, Tian, P, Huang, B, Feng, J, et al. Prevalence and prognostic importance of malnutrition, as assessed by four different scoring systems, in elder patients with heart failure. Nutr Metab Cardiovasc Dis. (2023) 33:978–86. doi: 10.1016/j.numecd.2023.01.004

PubMed Abstract | Crossref Full Text | Google Scholar

21. Li, J, Zhu, N, Wang, C, You, LP, Guo, WL, Yuan, ZH, et al. Preoperative albumin-to-globulin ratio and prognostic nutritional index predict the prognosis of colorectal cancer: a retrospective study. Sci Rep. (2023) 13:17272. doi: 10.1038/s41598-023-43391-5

PubMed Abstract | Crossref Full Text | Google Scholar

22. Laaban, JP. Nutrition and chronic respiratory failure. Ann Med Interne (Paris). (2000) 151:542–8. Nutrition et insuffisance respiratoire chronique.

PubMed Abstract | Google Scholar

23. Benjamin, JT, Plosa, EJ, Sucre, JM, van der Meer, R, Dave, S, Gutor, S, et al. Neutrophilic inflammation during lung development disrupts elastin assembly and predisposes adult mice to COPD. J Clin Invest. (2021) 131:e139481. doi: 10.1172/JCI139481

PubMed Abstract | Crossref Full Text | Google Scholar

24. Barnes, PJ. Inflammatory endotypes in COPD. Allergy. (2019) 74:1249–56. doi: 10.1111/all.13760

Crossref Full Text | Google Scholar

25. Gabriele, M, and Pucci, L. Diet bioactive compounds: implications for oxidative stress and inflammation in the vascular system. Endocr Metab Immune Disord Drug Targets. (2017) 17:264–75. doi: 10.2174/1871530317666170921142055

PubMed Abstract | Crossref Full Text | Google Scholar

26. Itoh, M, Tsuji, T, Nemoto, K, Nakamura, H, and Aoshiba, K. Undernutrition in patients with COPD and its treatment. Nutrients. (2013) 5:1316–35. doi: 10.3390/nu5041316

PubMed Abstract | Crossref Full Text | Google Scholar

27. Ellingsgaard, H, Hauselmann, I, Schuler, B, Habib, AM, Baggio, LL, Meier, DT, et al. Interleukin-6 enhances insulin secretion by increasing glucagon-like peptide-1 secretion from L cells and alpha cells. Nat Med. (2011) 17:1481–9. doi: 10.1038/nm.2513

PubMed Abstract | Crossref Full Text | Google Scholar

28. Wirsdorfer, F, and Jendrossek, V. The role of lymphocytes in radiotherapy-induced adverse late effects in the lung. Front Immunol. (2016) 7:591. doi: 10.3389/fimmu.2016.00591

PubMed Abstract | Crossref Full Text | Google Scholar

29. Eckart, A, Struja, T, Kutz, A, Baumgartner, A, Baumgartner, T, Zurfluh, S, et al. Relationship of nutritional status, inflammation, and serum albumin levels during acute illness: a prospective study. Am J Med. (2020) 133:713–722.e7. doi: 10.1016/j.amjmed.2019.10.031

PubMed Abstract | Crossref Full Text | Google Scholar

30. Paliogiannis, P, Fois, AG, Sotgia, S, Mangoni, AA, Zinellu, E, Pirina, P, et al. Neutrophil to lymphocyte ratio and clinical outcomes in COPD: recent evidence and future perspectives. Eur Respir Rev. (2018) 27:170113. doi: 10.1183/16000617.0113-2017

Crossref Full Text | Google Scholar

31. Ye, C, Yuan, L, Wu, K, Shen, B, and Zhu, C. Association between systemic immune-inflammation index and chronic obstructive pulmonary disease: a population-based study. BMC Pulm Med. (2023) 23:295. doi: 10.1186/s12890-023-02583-5

PubMed Abstract | Crossref Full Text | Google Scholar

32. Liu, H, Tan, X, Liu, Z, Ma, X, Zheng, Y, Zhu, B, et al. Association between diet-related inflammation and COPD: findings from NHANES III. Front Nutr. (2021) 8:732099. doi: 10.3389/fnut.2021.732099

PubMed Abstract | Crossref Full Text | Google Scholar

33. Liu, Z, Su, Y, Chen, Q, Xiao, L, Zhao, X, Wang, F, et al. Association of Dietary intake of vitamin E with chronic obstructive pulmonary disease events in US adults: a cross-sectional study of NHANES 2013-2018. Front Nutr. (2023) 10:1124648. doi: 10.3389/fnut.2023.1124648

PubMed Abstract | Crossref Full Text | Google Scholar

34. Ibrahimou, B, Azim, SI, and Sun, N. Interaction between blood lead level and chronic obstructive pulmonary disease (COPD) on risk of heart attack or stroke: USA NHANES, 2013-2014. Pulm Pharmacol Ther. (2019) 58:101805. doi: 10.1016/j.pupt.2019.101805

PubMed Abstract | Crossref Full Text | Google Scholar

35. Ruan, Z, Li, D, Cheng, X, Jin, M, liu, Y, Qiu, Z, et al. The association between sleep duration, respiratory symptoms, asthma, and COPD in adults. Front Med (Lausanne). (2023) 10:1108663. doi: 10.3389/fmed.2023.1108663

PubMed Abstract | Crossref Full Text | Google Scholar

36. Barnes, PJ, Shapiro, SD, and Pauwels, RA. Chronic obstructive pulmonary disease: molecular and cellular mechanisms. Eur Respir J. (2003) 22:672–88. doi: 10.1183/09031936.03.00040703

Crossref Full Text | Google Scholar

37. Iddir, M, Brito, A, Dingeo, G, Fernandez del Campo, SS, Samouda, H, la Frano, MR, et al. Strengthening the immune system and reducing inflammation and oxidative stress through diet and nutrition: considerations during the COVID-19 crisis. Nutrients. (2020) 12:1562. doi: 10.3390/nu12061562

Crossref Full Text | Google Scholar

38. Lauridsen, C. From oxidative stress to inflammation: redox balance and immune system. Poult Sci. (2019) 98:4240–6. doi: 10.3382/ps/pey407

Crossref Full Text | Google Scholar

39. Ochs-Balcom, HM, Grant, BJ, Muti, P, Sempos, CT, Freudenheim, JL, Browne, RW, et al. Antioxidants, oxidative stress, and pulmonary function in individuals diagnosed with asthma or COPD. Eur J Clin Nutr. (2006) 60:991–9. doi: 10.1038/sj.ejcn.1602410

Crossref Full Text | Google Scholar

40. Rodríguez-Rodríguez, E, Ortega, RM, Andrés, P, Aparicio, A, González-Rodríguez, LG, López-Sobaler, AM, et al. Antioxidant status in a group of institutionalised elderly people with chronic obstructive pulmonary disease. Br J Nutr. (2016) 115:1740–7. doi: 10.1017/S0007114516000878

PubMed Abstract | Crossref Full Text | Google Scholar

41. Kaluza, J, Larsson, SC, Orsini, N, Linden, A, and Wolk, A. Fruit and vegetable consumption and risk of COPD: a prospective cohort study of men. Thorax. (2017) 72:500–9. doi: 10.1136/thoraxjnl-2015-207851

PubMed Abstract | Crossref Full Text | Google Scholar

42. Kaluza, J, Harris, HR, Linden, A, and Wolk, A. Long-term consumption of fruits and vegetables and risk of chronic obstructive pulmonary disease: a prospective cohort study of women. Int J Epidemiol. (2018) 47:1897–909. doi: 10.1093/ije/dyy178

PubMed Abstract | Crossref Full Text | Google Scholar

43. Hogan, D, Lan, LT, Diep, DT, Gallegos, D, and Collins, PF. Nutritional status of Vietnamese outpatients with chronic obstructive pulmonary disease. J Hum Nutr Diet. (2017) 30:83–9. doi: 10.1111/jhn.12402

PubMed Abstract | Crossref Full Text | Google Scholar

44. Collins, PF, Yang, IA, Chang, YC, and Vaughan, A. Nutritional support in chronic obstructive pulmonary disease (COPD): an evidence update. J Thorac Dis. (2019) 11:S2230–7. doi: 10.21037/jtd.2019.10.41

PubMed Abstract | Crossref Full Text | Google Scholar

45. Ezzell, L, and Jensen, GL. Malnutrition in chronic obstructive pulmonary disease. Am J Clin Nutr. (2000) 72:1415–6. doi: 10.1093/ajcn/72.6.1415

Crossref Full Text | Google Scholar

46. Chai, X, Chen, Y, Li, Y, Chi, J, and Guo, S. Lower geriatric nutritional risk index is associated with a higher risk of all-cause mortality in patients with chronic obstructive pulmonary disease: a cohort study from the National Health and nutrition examination survey 2013-2018. BMJ Open Respir Res. (2023) 10:e001518. doi: 10.1136/bmjresp-2022-001518

Crossref Full Text | Google Scholar

47. Suzuki, E, Kawata, N, Shimada, A, Sato, H, Anazawa, R, Suzuki, M, et al. Prognostic nutritional index (PNI) as a potential prognostic tool for exacerbation of COPD in elderly patients. Int J Chron Obstruct Pulmon Dis. (2023) 18:1077–90. doi: 10.2147/COPD.S385374

PubMed Abstract | Crossref Full Text | Google Scholar

48. Lo Buglio, A, Scioscia, G, Bellanti, F, Tondo, P, Soccio, P, Natale, MP, et al. Controlling nutritional status score as a predictor for chronic obstructive pulmonary disease exacerbation risk in elderly patients. Meta. (2023) 13:1123. doi: 10.3390/metabo13111123

Crossref Full Text | Google Scholar

49. Cederholm, T, Jensen, GL, Correia, M, Gonzalez, MC, Fukushima, R, Higashiguchi, T, et al. GLIM criteria for the diagnosis of malnutrition - a consensus report from the global clinical nutrition community. Clin Nutr. (2019) 38:1–9. doi: 10.1016/j.clnu.2018.08.002

PubMed Abstract | Crossref Full Text | Google Scholar

50. Zhang, Z, Pereira, SL, Luo, M, and Matheson, EM. Evaluation of blood biomarkers associated with risk of malnutrition in older adults: a systematic review and meta-analysis. Nutrients. (2017) 9:829. doi: 10.3390/nu9080829

Crossref Full Text | Google Scholar

51. Chung, KF, and Adcock, IM. Multifaceted mechanisms in COPD: inflammation, immunity, and tissue repair and destruction. Eur Respir J. (2008) 31:1334–56. doi: 10.1183/09031936.00018908

PubMed Abstract | Crossref Full Text | Google Scholar

52. Yang, Y, Mao, J, Ye, Z, Li, J, Zhao, H, and Liu, Y. Risk factors of chronic obstructive pulmonary disease among adults in Chinese mainland: a systematic review and meta-analysis. Respir Med. (2017) 131:158–65. doi: 10.1016/j.rmed.2017.08.018

PubMed Abstract | Crossref Full Text | Google Scholar

53. Adeloye, D, Song, P, Zhu, Y, Campbell, H, Sheikh, A, Rudan, I, et al. Global, regional, and national prevalence of, and risk factors for, chronic obstructive pulmonary disease (COPD) in 2019: a systematic review and modelling analysis. Lancet Respir Med. (2022) 10:447–58. doi: 10.1016/S2213-2600(21)00511-7

PubMed Abstract | Crossref Full Text | Google Scholar

54. Chen, H, Liu, X, Gao, X, Lv, Y, Zhou, L, Shi, J, et al. Epidemiological evidence relating risk factors to chronic obstructive pulmonary disease in China: a systematic review and meta-analysis. PLoS One. (2021) 16:e0261692. doi: 10.1371/journal.pone.0261692

PubMed Abstract | Crossref Full Text | Google Scholar

55. Hancu, A. Nutritional status as a risk factor in COPD. Maedica (Bucur). (2019) 14:140–3. doi: 10.26574/maedica.2019.14.2.140

PubMed Abstract | Crossref Full Text | Google Scholar

56. Barnes, PJ. Oxidative stress-based therapeutics in COPD. Redox Biol. (2020) 33:101544. doi: 10.1016/j.redox.2020.101544

PubMed Abstract | Crossref Full Text | Google Scholar

57. Duran-Güell, M, Flores-Costa, R, Casulleras, M, López-Vicario, C, Titos, E, Díaz, A, et al. Albumin protects the liver from tumor necrosis factor alpha-induced immunopathology. FASEB J. (2021) 35:e21365. doi: 10.1096/fj.202001615RRR

PubMed Abstract | Crossref Full Text | Google Scholar

58. Zinellu, E, Fois, AG, Sotgiu, E, Mellino, S, Mangoni, AA, Carru, C, et al. Serum albumin concentrations in stable chronic obstructive pulmonary disease: a systematic review and Meta-analysis. J Clin Med. (2021) 10:269. doi: 10.3390/jcm10020269

Crossref Full Text | Google Scholar

59. du, W, Guan, H, Wan, X, Zhu, Z, Yu, H, Luo, P, et al. Circulating liver function markers and the risk of COPD in the UK biobank. Front Endocrinol (Lausanne). (2023) 14:1121900. doi: 10.3389/fendo.2023.1121900

PubMed Abstract | Crossref Full Text | Google Scholar

60. Hao, W, Li, M, Zhang, Y, Zhang, C, and Wang, P. Severity of chronic obstructive pulmonary disease with ‘exacerbator with emphysema phenotype’ is associated with potential biomarkers. Postgrad Med J. (2020) 96:28–32. doi: 10.1136/postgradmedj-2019-136599

PubMed Abstract | Crossref Full Text | Google Scholar

61. Thomas, MR, and Storey, RF. The role of platelets in inflammation. Thromb Haemost. (2015) 114:449–58. doi: 10.1160/TH14-12-1067

Crossref Full Text | Google Scholar

62. Ellingsen, J, Janson, C, Bröms, K, Lisspers, K, Ställberg, B, Högman, M, et al. Neutrophil-to-lymphocyte ratio, blood eosinophils and COPD exacerbations: a cohort study. ERJ Open Res. (2021) 7:00471–2021. doi: 10.1183/23120541.00471-2021

PubMed Abstract | Crossref Full Text | Google Scholar

63. Foreman, MG, Zhang, L, Murphy, J, Hansel, NN, Make, B, Hokanson, JE, et al. Early-onset chronic obstructive pulmonary disease is associated with female sex, maternal factors, and African American race in the COPDGene study. Am J Respir Crit Care Med. (2011) 184:414–20. doi: 10.1164/rccm.201011-1928OC

PubMed Abstract | Crossref Full Text | Google Scholar

64. Sorheim, IC, Johannessen, A, Gulsvik, A, Bakke, PS, Silverman, EK, and DeMeo, DL. Gender differences in COPD: are women more susceptible to smoking effects than men? Thorax. (2010) 65:480–5. doi: 10.1136/thx.2009.122002

PubMed Abstract | Crossref Full Text | Google Scholar

65. Merkus, PJ, Borsboom, GJ, Van Pelt, W, Schrader, PC, Van Houwelingen, HC, Kerrebijn, KF, et al. Growth of airways and air spaces in teenagers is related to sex but not to symptoms. J Appl Physiol. (1985) 75:2045–53. doi: 10.1152/jappl.1993.75.5.2045

PubMed Abstract | Crossref Full Text | Google Scholar

66. DeMeo, DL. Sex and gender Omic biomarkers in men and women with COPD: considerations for precision medicine. Chest. (2021) 160:104–13. doi: 10.1016/j.chest.2021.03.024

PubMed Abstract | Crossref Full Text | Google Scholar

67. DeMeo, DL, Ramagopalan, S, Kavati, A, Vegesna, A, Han, MK, Yadao, A, et al. Women manifest more severe COPD symptoms across the life course. Int J Chron Obstruct Pulmon Dis. (2018) 13:3021–9. doi: 10.2147/COPD.S160270

PubMed Abstract | Crossref Full Text | Google Scholar

68. DeMeo, DL. The yin and Yang of COPD: sex/gender differences in the National Emphysema Treatment Trial. Am J Respir Crit Care Med. (2007) 176:222–3. doi: 10.1164/rccm.200704-558ED

Crossref Full Text | Google Scholar

69. Martinez, FJ, Curtis, JL, Sciurba, F, Mumford, J, Giardino, ND, Weinmann, G, et al. Sex differences in severe pulmonary emphysema. Am J Respir Crit Care Med. (2007) 176:243–52. doi: 10.1164/rccm.200606-828OC

PubMed Abstract | Crossref Full Text | Google Scholar

Keywords: advanced lung cancer inflammation index, chronic obstructive pulmonary disease, nutritional status, cross-sectional study, population-based study, NHANES

Citation: Xu Y, Yan Z, Li K, Liu L and Xu L (2024) Association between nutrition-related indicators with the risk of chronic obstructive pulmonary disease and all-cause mortality in the elderly population: evidence from NHANES. Front. Nutr. 11:1380791. doi: 10.3389/fnut.2024.1380791

Received: 02 February 2024; Accepted: 01 July 2024;
Published: 16 July 2024.

Edited by:

Tomoko Suzuki, Saitama Medical University, Japan

Reviewed by:

Yayun Nan, People’s Hospital of Ningxia Hui Autonomous Region, China
Chih-Yuan Ko, The Second Affiliated Hospital of Fujian Medical University, China

Copyright © 2024 Xu, Yan, Li, Liu and Xu. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Lei Xu, MTUzNTAyNTYyMDBAMTYzLmNvbQ==

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