Kaijiang Kang1,2,3,4†
Yu Wang1,2,3,4†
Jianwei Wu1,2,3,4Anxin Wang1,5,6
Jia Zhang1,2,3,4Jie Xu1,2,3,4Yi Ju1,2,3,4*
Xingquan Zhao1,2,3,4*- 1Department of Neurology, Beijing Tiantan Hospital, Capital Medical University, Beijing, China
- 2China National Clinical Research Center for Neurological Diseases, Beijing, China
- 3Center of Stroke, Beijing Institute for Brain Disorders, Beijing, China
- 4Beijing Key Laboratory of Translational Medicine for Cerebrovascular Disease, Beijing, China
- 5Department of Epidemiology and Health Statistics, School of Public Health, Capital Medical University, Beijing, China
- 6Beijing Municipal Key Laboratory of Clinical Epidemiology, Beijing, China
Background and Purpose: Intracranial atherosclerosis has gained increasing attention due to the high risk of recurrent clinical or subclinical ischemic events, while the relationship between low-density lipoprotein cholesterol (LDL-C) measured at a single time point and intracranial atherosclerotic stenosis (ICAS) is inconsistent. This study aims to assess the association between cumulative exposure to increased LDL-C and the prevalence of asymptomatic ICAS.
Methods: The Asymptomatic Polyvascular Abnormalities Community study was investigated on the epidemiology of asymptomatic polyvascular abnormalities in Chinese adults. In this study, we included 4,523 participants with LDL-C measured at 3 examinations in 2006, 2008, and 2010. Cumulative exposure to increased LDL-C was calculated as following: LDL-C burden2006−2008 = [(LDL-C2006-1.8) + (LDL-C2008-1.8)]/2 * time2006−2008; LDL-C burden = LDL-C burden2006−2008 + LDL-C burden2008−2010. Transcranial doppler ultrasonography was performed in 2010 to detecting the ICAS.
Results: Of the 4,347 patients, 13.3% (580/4,347) were diagnosed with ICAS. In univariate analysis, the association between LDL-C burden and ICAS prevalence was significant, the odds ratios (95% confidence interval) from the lowest to the highest quartile were 1 (reference), 1.30 (0.99–1.70), 1.32 (1.01–1.73), and 2.14 (1.66–2.75), respectively (P < 0.05). After adjustment for potential confounding factors, the same result was reached.
Conclusions: Cumulative exposure to increased LDL-C is concentration-dependently associated with increased prevalence of asymptomatic ICAS, especially in those under the age of 65 y or free of hypertension, diabetes mellitus, and hyperlipidemia.
Introduction
Stroke has now become the most common and disabling disease in China, and ischemic stroke is the primary type (1, 2). Intracranial atherosclerosis has gained increasing attention due to the high risk of recurrent clinical, subclinical ischemic events, and its association with cognitive deficits, especially in non-whites (3, 4). Extracranial atherosclerotic stenosis (ECAS) is more prevalent in the Caucasian population, while intracranial atherosclerotic stenosis (ICAS) is one of the leading causes of ischemic stroke in Asian populations due to the differences in race and lifestyle (1, 2, 5, 6). Some studies have shown that hyperlipidemia, especially increased low-density lipoprotein cholesterol (LDL-C), is an independent risk factor for atherosclerotic stenosis and vulnerable plaque of ECAS (7–9). However, the relationship between the lipid levels measured at a single time point and ICAS is still inconsistent (10–13). Some studies suggested that higher LDL-C levels might be associated with increased risk of ICAS (14). Therefore, this community-based, epidemiological and observational study was conducted to explore the association between cumulative exposure to increased LDL-C and the prevalence of ICAS in the Asymptomatic Polyvascular Abnormalities Community (APAC) study.
Materials and Methods
Study Design and Population
The APAC study is a subset of the Kailuan study, investigating the prevalence and associations of asymptomatic multivascular abnormalities in a large industrial population in China (15). A total of 5,440 participants met the inclusion criteria of the APAC study: (1) aged ≥ 40 years; (2) without a history of cardiovascular or cerebrovascular disease. After excluding 917 participants with missing data of LDL-C at 2006, 2008 or 2010 time points, and 176 participants with poor temporal window, 4,347 participants (2,638 men and 1,709 women) were eventually included with full baseline data collected from 2006 to 2010 (Figure 1).
Figure 1. Study flow chart.
Measurement of Lipid Levels
Peripheral blood samples were taken from the antecubital vein under fasting conditions and analyzed within 4 h using an auto-analyzer (Hitachi 747; Hitachi, Tokyo, Japan). Lipid parameters, including LDL-C, high-density lipoprotein cholesterol (HDL-C), total cholesterol (TC), and triglyceride (TG), were measured at three examinations in 2006, 2008, and 2010. The specific methods of lipid levels measurement had been described in published articles (8, 9).
Calculation of LDL-C Burden
Cumulative exposure to increased LDL-C was calculated as the weighted sum of the average LDL-C level:
LDL-C burden2006−2008 = [(LDL-C2006-1.8) + (LDL-C2008-1.8)]/2 * time2006−2008;
LDL-C burden2008−2010 = [(LDL-C2008-1.8) + (LDL-C2010-1.8)]/2 * time2008−2010;
LDL-C burden = LDL-C burden2006−2008 + LDL-C burden2008−2010.
The cutoff value of LDL-C is set at 1.8 mmol/L (70 mg/dL) according to the SPARCL study, which indicated that achieving an LDL-C level of <1.8 mmol/L was associated with a significant reduction in risk of stroke (16). Participants were classified into four groups (Q1, Q2, Q3, and Q4) according to the interquartile range of LDL-C burden.
Measurement of Potential Covariates at Baseline
Demographic information, past medical history, and current medications were collected at baseline through a standard questionnaire. Current smoker refers to smoking at least one cigarette per day. Body mass index (BMI) was calculated according to the following equation based on the weight and height: BMI = weight (kg)/square of height (m2). Physical activity was categorized as none, seldom, and always. Except for the lipid indicators, systolic and diastolic blood pressure, fasting blood glucose (FBG, hexokinase/glucose-6-phosphate dehydrogenase method) and uric acid (UA, uricase-peroxidase method) were also measured.
Assessment of Intracranial Atherosclerosis Stenosis
Transcranial doppler ultrasonography (TCD), as a reliable method to diagnose ICAS, was performed by two experienced technicians (blinded to the baseline information of the participants) in 2010 for the detection of ICAS using portable devices (EME Companion, Nicolet, Madison, WI, USA). ICAS was diagnosed according to the peak flow velocity criteria which was published and validated against MR angiography and clinical outcomes (17, 18). Details were described in a previous study. In brief, ICAS was diagnosed if a peak systolic flowing velocity > 140 cm/s for the middle cerebral artery; >120 cm/s for the anterior cerebral artery and internal carotid siphon; and >100 cm/s for the posterior cerebral artery and vertebral-basilar. Also, we considered age, the presence of segmental abnormal velocity, disturbance in echo frequency, or turbulence sound in the diagnosis of ICAS. In this study, the ICAS was diagnosed if stenosis or occlusion was found in one of the studied cranial arteries by TCD, and the participants with poor temporal window were excluded.
Statistical Analysis
The statistical analysis was performed using a commercial statistical software package (SAS 9.1, Cary, NC, USA). T-test or analysis of variance (continuous variables) and chi-squared tests (categorical variables) were used to analyze the differences of baseline characteristics between patients with and without ICAS. Chi-squared tests and logistic regression were used to evaluate the relationship between LDL-C burden levels and ICAS prevalence. Differences of p value < 0.05 were considered statistically significant for two-tailed tests.
Results
Prevalence of ICAS
Of the 4,347 participants, 580 (13.3%) of them were detected as having asymptomatic ICAS based on the TCD results. The overall distribution and proportion of ICAS in each vessel have been described previously (10, 19).
Baseline Characteristics
Compared to those without ICAS, the subjects with ICAS were older, with larger BMI, fewer daily activities, higher prevalence of hypertension, DM, hyperlipidemia and current medication in use; and higher levels of systolic or diastolic blood pressure and FBG (p < 0.05, Table 1). In addition, when comparing the baseline characteristics according to quartile of LDL-C burden, there were significant differences in age, sex, BMI, physical activity, income status, hypertension, hyperlipidemia, smoking, drinking, systolic and diastolic blood pressure, FBG, and UA.
Table 1. Baseline characteristics of the participants with or without ICAS.
Correlation Between LDL-C Burden and the Prevalence of Asymptomatic ICAS
There were significant differences in LDL-C levels measured in 2006, 2008, and 2010 between participants with ICAS and those without ICAS (p < 0.05) (Table 2). There were also significant differences in LDL-C burden, LDL-C burden2006−2008, and LDL-C burden2008−2010 between participants with ICAS and those without ICAS (p < 0.01) (Table 2). In univariate analysis, the association between LDL-C burden and prevalence of asymptomatic ICAS was significant (p < 0.01). Compared with participants in the Q1 group, the Q2, Q3, and Q4 groups had significantly increased prevalence of asymptomatic ICAS with ORs of 1.30 (0.99–1.70), 1.32 (1.01–1.73), and 2.14 (1.66–2.75), respectively (p < 0.05). In multivariate analysis, after adjustment for age, gender, smoking, drinking, BMI, hypertension, diabetes mellitus (DM), hyperlipidemia, physical activity, income status, antihypertensive medication, antidiabetic medication, and lipid-lowering medication, similar and significant associations were also observed with ORs of 1 (reference), 1.33 (1.01–1.76), 1.41 (1.07–1.87), and 2.12 (1.63– 2.76) from the lowest to the highest quartile (p < 0.05) (Table 3).
Table 2. LDL-C and LDL-C burden levels of the participants with or without ICAS.
Table 3. Association between LDL-C burden and the prevalence of asymptomatic ICAS.
In the sensitivity analysis, after excluding the subjects with age ≥ 65 y or the subjects with a history of hypertensive, DM, or hyperlipidemia, the association between LDL-C burden and the prevalence of asymptomatic ICAS was still statistically significant (p < 0.01), additional information was demonstrated in Table 3.
Discussion
To the best of our knowledge, this is the first investigation using the LDL-C burden to demonstrate the association between LDL-C levels and the asymptomatic ICAS prevalence. In this large and retrospective cohort study, we disclosed that cumulative exposure to increased LDL-C was concentration-dependently associated with asymptomatic ICAS prevalence, especially in those under the age of 65 years or free of hypertension, DM, and hyperlipidemia.
ICAS had been reported to account for about 30–50% of ischemic stroke or transient ischemic attacks in Asia and often results in poor prognosis (3, 13). Confronting with the situation, there is a considerable need to identify and control risk factors of ICAS. It was suggested that hyperlipidemia and higher LDL-C levels were associated with increased risk of ICAS in previous studies based on TCD, computed tomography angiography (CTA), and high-resolution magnetic resonance angiography (HR-MRA) (14, 20, 21). While, no significant association was found in the Chinese Intracranial Atherosclerosis (CICAS) study (22), and only the highest quintile of LDL-C, measured at a single time point, was associated with the prevalence of ICAS in the APAC study (19). The fact that LDL-C levels fluctuate over time within individuals was ignored by previous studies based on a single time point assessment and likely to generate biased estimates of its association with ICAS. Although the LDL-C level has been the primary target for lipid-lowering treatment in the prevention of cardiovascular and cerebrovascular disease in clinical practice, the role of LDL-C in ICAS remains to be elucidated (3, 23–25). The strengths of this study relate to the large sample size of subjects to find the significant association of sustained and increased LDL-C with an elevated risk of ICAS prevalence. As we know, LDL-C levels will be affected by some factors such as participants' short-term diet and physical activity, so one single time point measurement of LDL-C level could not reflect the participants' long-term actual LDL-C level. Instead, LDL-C burden, calculated as the weighted sum of the average LDL-C levels, is a more reliable indicator of long-term LDL-C levels.
The critical process involved in arteriosclerosis is the retention and accumulation of cholesterol-rich lipoproteins (especially LDL) within the arterial intima at sites of predilection for plaque formation (26–29). When the concentration of LDL-C increases to a certain extent, the probability of intimal retention of LDL and the initiation or progressive development of atherosclerosis increases (27, 29, 30). As a well-established risk factor of atherosclerosis, LDL-C has been actually proved not merely a biomarker of increased risk but a causal factor in the pathophysiology of atherosclerotic cardiovascular disease (26), which has prompted us to further investigate the association of LDL-C with the prevalence of ICAS.
Considering that old age, hypertension, DM, hyperlipidemia are previously documented risk factors for ICAS, we performed further sensitivity analysis (13, 21, 31). After excluding the subjects with age ≥ 65 y or those with a history of hypertensive, DM, or hyperlipidemia, the same result was obtained with higher ORs in concentration-depend manners, which indicated that LDL-C burden was concentration-dependently associated with the prevalence of asymptomatic ICAS, especially in those with age < 65 y and those without a history of hypertension, DM, or hyperlipidemia.
Based on the current research results, LDL-C appears to be associated with asymptomatic ICAS. Although LDL-C has been a primary target for lipid-lowering therapy in the prevention of ischemic stroke, whether there is a causal relationship between LDL-C and asymptomatic ICAS remains unclear. Miao et al. reported that the degree of stenosis in asymptomatic ICAS can be alleviated with intensive lipid-lowering therapy using statin for Chinese patients with asymptomatic ICAS (32). Chung et al. found that high-dose statin treatment can significantly decrease the LDL-C levels and effectively stabilize symptomatic intracranial atherosclerotic plaques as documented by HR-MRI (33). Evidence above suggests that LDL-C may play a role in the formation and progression of ICAS, and maintaining LDL in a normal range may be the right choice for preventing ICAS in clinical practice. Given the high prevalence of ICAS and increased risk of ischemic stroke, more researches on mechanisms and prospective intervention studies are needed to provide insight into their relationship.
There were some limitations in our study. First, some participants with nonatherosclerotic diseases may also be included in the presumed ICAS group. Second, our study was based on a randomly selected subgroup of participants of the Kailuan Study that included employees and retirees of the Kailuan Co. Ltd. and the study population was selected using a stratified random sampling method by age and sex. It may not be representative of the population of the Tangshan area in Hebei province despite the large study sample. Third, ICAS was only determined at a single time point in 2010 and no baseline assessment of ICAS was made in 2006 among the participants. Forth, we just investigated the cumulative effect of blood lipid but not other factors on ICAS. Despite these limitations, this was the first large, cohort study to our knowledge that investigate the correlation between LDL-C burden and asymptomatic ICAS so far.
In conclusion, our data show that cumulative exposure to increased LDL-C is concentration-dependently associated with increased prevalence of asymptomatic ICAS, especially in those with age < 65 y and free of hypertension, DM, and hyperlipidemia.
Data Availability Statement
The raw data supporting the conclusions of this article will be made available by the authors, without undue reservation.
Ethics Statement
The studies involving human participants were reviewed and approved by the Ethics Committees of the Kailuan General Hospital and Beijing Tiantan Hospital. The patients/participants provided their written informed consent to participate in this study.
Author Contributions
KK and YW interpreted the data and drafted the manuscript. YJ and XZ conceived and designed the research. AW acquired and analyzed the data. JW and JZ made a critical revision of the manuscript. All authors revised and agreed to be accountable for the content of this work.
Funding
This study was sponsored by Capital health research and development of special (Grant Number: Capital 2011-2004-03) and Beijing Municipal Science & Technology Commission, PR China (Grant Number: Z131107002213009).
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.
Acknowledgments
We thank all the patients and healthcare providers who participated in the present study for their important contributions.
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Keywords: epidemiology, LDL-C, intracranial atherosclerotic stenosis, risk factor, TCD
Citation: Kang K, Wang Y, Wu J, Wang A, Zhang J, Xu J, Ju Y and Zhao X (2020) Association Between Cumulative Exposure to Increased Low-Density Lipoprotein Cholesterol and the Prevalence of Asymptomatic Intracranial Atherosclerotic Stenosis. Front. Neurol. 11:555274. doi: 10.3389/fneur.2020.555274
Received: 24 April 2020; Accepted: 05 November 2020;
Published: 26 November 2020.
Edited by:
Maurizio A. Leone, Casa Sollievo della Sofferenza (IRCCS), ItalyReviewed by:
Gyeong-Moon Kim, Sungkyunkwan University, South KoreaKota Maekawa, Kobe City Medical Center General Hospital, Japan
Copyright © 2020 Kang, Wang, Wu, Wang, Zhang, Xu, Ju and Zhao. 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: Yi Ju, juyi1226@vip.163.com; Xingquan Zhao, zxq@vip.163.com
†These authors have contributed equally to this work and share first authorship