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ORIGINAL RESEARCH article

Front. Public Health, 26 October 2022
Sec. Clinical Diabetes

Lower hydration status increased diabetic retinopathy among middle-aged adults and older adults: Results from NHANES 2005-2008

  • 1Department of Nutrition, Beijing Luhe Hospital, Capital Medical University, Beijing, China
  • 2Institute of Reproductive and Child Health/National Health Commission Key Laboratory of Reproductive Health, Peking University, Beijing, China
  • 3Department of Epidemiology and Biostatistics, School of Public Health, Peking University, Beijing, China

Background: Diabetic retinopathy (DR) is a common complication of diabetic patients. Retinal physiological function is affected by hydration status. We aimed to explore the association between hydration status and DR.

Methods: National Health and Nutrition Examination Survey (NHANES) 2005-2008 was used to perform this cross-sectional study. Serum osmolality was used to assess hydration status for all participants and calculated osmolality was evaluated for only older people. DR and its severity were evaluated and graded into mild non-proliferative retinopathy, moderate/severe non-proliferative retinopathy, and proliferative diabetic retinopathy by the Early Treatment for Diabetic Retinopathy Study protocol and NHANES Digital Grading Protocol. Fully adjusted multivariable logistic regression models were used by SAS OnDemand for Academics.

Results: Among the 5,220 United States adults aged 40 or older, compared with the lowest osmolality group, participants with the highest quartile of serum osmolarity had higher odds of DR (OR: 1.371, 95% CI: 1.001–1.876). For participants with DR, the adjusted OR (95 % CI) of moderate/severe non-proliferative retinopathy and proliferative diabetic retinopathy in the higher serum osmolarity group was 2.119 (1.200–3.741) and 7.001 (3.175–15.438), respectively. Furthermore, in older people, higher calculated osmolarity was significantly associated with increased occurrence of DR (OR: 2.039, 95% CI: 1.305–3.186).

Conclusions: Adults with lower hydration status had higher risk of DR, moderate/severe non-proliferative retinopathy, and proliferative diabetic retinopathy. Dehydration in older adults, classified by calculated osmolality, is associated with a higher rate of DR. There was consistent trend in the results between the two methods.

Introduction

Diabetic retinopathy (DR) is one of the most common complications of diabetes mellitus (DM) and is the major cause of visual loss in working-age adults (1, 2). Although extensive studies and health promotion programs on DM and its complications have been of great concern, it was reported that 103.12 million adults worldwide had DR in 2020, and this number was expected to be 160.50 million by 2045 (3). Furthermore, the age-standardized global prevalence of blindness due to DR has also increased by 14.9% from 1990 to 2020, placing a significant burden on public health (4).

Appropriate hydration status is the basis for healthy metabolism (5). Dehydration, often classified as isotonic or hypotonic dehydration (equal or more solute loss than water) and hypertonic dehydration (greater water loss than solutes), refers to a decrease in total body water when the fluid lost cannot be entirely replenished by fluid intake (6, 7). Previous evidence has indicated that the risks of urological, gastrointestinal, circulatory, and neurological diseases increase with dehydration (8). People who are dehydrated also have higher mortality and lower quality of life if not treated well (9). In addition, hydration status was reported to affect the retinal physiological function (10). For instance, dehydration can contribute to lower peak systolic velocity of the central retinal artery, as well as decreased retinal nerve fiber layer thickness and macular volume, all of which are risk factors of DR (1114).

It's widely known that polyuria is a common symptom in people with diabetes. With age, the sensation of thirst blunts, primary urine concentration declines, muscle mass decreases, and total body water and fluid stores decrease, which may increase the risks of dehydration (1518). Furthermore, age-related pathophysiological changes like the concentration change of Na+, K+, and Cl and comorbidities such as hyperglycemia, nephrotic syndrome, and adrenal insufficiency may also result in dehydration (10, 19). Hence, older diabetics are more likely to be influenced by fluid and electrolyte balance disturbances, which may lead to a higher risk of hypertonic dehydration and induce further DR (20, 21). However, limited studies have examined the association of hydration status with DR.

To fill these research gaps, we used data from the National Health and Nutrition Examination Survey (NHANES) 2005-2008 to explore the association between hydration status and DR among middle-aged and older United States adults.

Materials and methods

Study population

The NHANES is a cross-sectional survey designed to assess the health and nutritional status of the community dwelling populations in the United States. It started in the early 1960s and has been a continuous program since 1999. Every year, the NHANES collected data from a nearly 5,000-person nationally representative sample. Each participant completed the interview, examination and laboratory tests. The National Center for Health Statistics Website (https://www.cdc.gov/nchs/nhanes/) contains the NHANES data that are available to the general public. The NHANES protocols were approved by the National Center for Health Statistics Research Ethics Review Board. All participants provided written informed consent for this survey.

We used the demographics, dietary, examination, laboratory, and questionnaire data from NHANES 2005–2008. A total of 5,704 participants aged 40 years or older completed the retinal imaging exams. Participants who were blind or had eye infections/patches on both eyes were excluded from this study. According to the flow chart shown in Figure 1, we excluded 4 participants whose education level or marital status questionnaires were incomplete, 126 participants without BMI or blood pressure data, 99 participants without information on smoking or alcohol use, 5 participants who were pregnant, 206 participants without data on blood osmolality, sodium, potassium, glucose, urea nitrogen, glycohemoglobin, and total cholesterol, and 44 participants without information about prescription medications or comorbidities. Finally, 5,220 adults were involved in this study.

FIGURE 1
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Figure 1. Flow chart of the study.

Ascertainment of hydration status

In order to assess and grade the hydration status, serum osmolality was ranked and divided into four groups, the lowest osmolality group (serum osmolality ≤ 275 mOsm/kg), the lower osmolality group (276–279 mOsm/kg), the higher osmolality group (280–282 mOsm/kg), and the highest osmolality group (≥ 283 mOsm/kg) (9, 22).

Considering the impaired pancreatic and renal function of diabetes, we also used calculated osmolarity to evaluate the hydration status of people aged 65 or older for wider application in clinical practice (15, 2123).

Calculated Osmolarity=1.86×(Na++K+)+1.15×glucose                                                    +urea+14

In this equation, blood sodium, potassium, glucose, and urea nitrogen were all measured in mmol/L and were represented by Na+, K+, glucose, and urea , respectively. Normal hydration (285–294 mmol/L), impending dehydration (295–300 mmol/L), current dehydration (> 300 mmol/L), and hyperhydration (< 285 mmol/L) were the four grades used to categorize the hydration status (23, 24).

Ascertainment of DR

In participants aged 40 years and older, forty-five-degree non-mydriatic digital retinal images of each eye were captured. EyeQ Lite image processing software was used to view each retinal image. The ophthalmic digital imaging system was used to assess the presence of retinal diseases. DR severity levels were graded by graders at the University of Wisconsin and were classified into no retinopathy, mild non-proliferative retinopathy (NPR), moderate/severe NPR, and proliferative retinopathy (PDR), by the NHANES Digital Grading Protocol (25).

Covariates

Information on age (40–64 years, ≥ 65 years), sex (male, female), race (non-Hispanic White, other races), education (under high school, high school or equivalent, and above high school), marital status (married: married/lived with partners; not married: widowed/divorced/separated/never married), and smoke status (current, ever, and never) were all obtained by self-reported. Participants who had smoked more than 100 cigarettes in life were considered as current smoking (current smokers) or ever smoking (former smokers); participants who had smoked < 100 cigarettes in life were considered as never smoking. Body mass index (BMI) was calculated as weight (kg) divided by the square of height (m) and was categorized into normal weight (< 25.0 kg/m2), overweight (25.0–29.9 kg/m2), and obese (≥ 30.0 kg/m2), which was measured in the mobile examination centers (MECs). Alcohol consumption (0 gram, 0–20 grams, and >20 grams) was assessed from a 24-h dietary recall. The concentrations of blood glycohemoglobin (< 7.0%, ≥ 7.0%), serum cholesterol (< 5.1 mmol/L, ≥ 5.1 mmol/L), and serum albumin (< 35 g/L, ≥ 35 g/L) might have an impact on retinopathy (2630). Comorbidities such as hypertension (systolic pressure ≥130 mmHg or diastolic pressure ≥80 mmHg), liver conditions, thyroid problem, congestive heart failure (CHF), and asthma, and the use of diuretics were included because they were associated with DR or water metabolism (26, 27, 3136). Ophthalmic imaging status (complete, partial) was also taken into account since some participants did not complete the entire imaging process due to multiple causes, including physical limitations of eyes and equipment failure.

Statistical analysis

SAS OnDemand for Academics was applied to complete statistical analyses. Weights were utilized to match total population counts because of the complex survey design, non–response, and post-stratification adjustment. The chi-square test of the Rao-Scott modified weight was used to examine the subject characteristics at baseline, including age, sex, race, education, marital status, BMI, smoke status, alcohol consumption, blood glycohemoglobin, serum total cholesterol, serum albumin, comorbidities, use of diuretics, and ophthalmic imaging status. Multivariable logistic regression models were constructed by surveylogistic procedure with sampling weight, cluster, and strata. Model 1 was unadjusted and Model 2 was adjusted for age, sex, and race. Based on Model 2, Model 3 was further adjusted for all the other covariates. P value of < 0.05 or 95% confidence intervals (95% CI) that did not cross 1.00 was considered statistically significant.

Results

Subject characteristics

This study included 5,220 United States participants in total. Adults with DR (n = 641) were more likely to be older, male, of other races, with lower education level, alcohol consumption, serum total cholesterol, and serum albumin, as well as having higher BMI, glycohemoglobin, and prevalence of hypertension and CHF than adults without retinopathy (n = 4,579) (Table 1).

TABLE 1
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Table 1. Characteristics of United States participants grouped by with or without DR, NHANES 2005-2008.

Association between serum osmolarity and DR

Figure 2 showed the odds ratios (ORs) and 95% CIs for DR based on serum osmolality level. After fully adjusted, participants with the highest quartile of serum osmolarity had higher odds of DR than those in the lowest osmolality group (OR: 1.371, 95% CI: 1.001–1.876).

FIGURE 2
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Figure 2. Associations of serum osmolarity with DR, NHANES 2005–2008. (A) Model 1: Unadjusted. (B) Model 2: Adjusted for age, sex, and race. (C) Model 3: Adjusted for age, sex, race, education, marital status, BMI, smoke status, alcohol consumption, blood glycohemoglobin, serum total cholesterol, serum albumin, comorbidities, use of diuretics, and ophthalmic imaging status. Q1, the lowest osmolality group (serum osmolality ≤ 275 mOsm/kg); Q2, the lower osmolality group (276–279 mOsm/kg); Q3, the higher osmolality group (280–282 mOsm/kg); Q4, the highest osmolality group (≥ 283 mOsm/kg).

Association between serum osmolarity and DR severity

Patients with DR (n = 641) were further classified into three groups based on the retinopathy severity, mild NPR (n = 521), moderate/severe NPR (n = 96), and PDR (n = 24), respectively. In the three groups, there are significant differences in race, BMI, smoke status, alcohol consumption, glycohemoglobin, serum albumin, and the use of diuretics (Table 2).

TABLE 2
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Table 2. Characteristics of DR patients grouped by severity, NHANES 2005-2008.

Figure 3 showed the association between serum osmolarity and DR severity. As the limited number of PDR patients, participants were divided into lower serum osmolarity group and higher serum osmolarity group, and liver condition was excluded from Model 3. After fully adjustment, the odds of moderate/severe NPR and PDR rose as serum osmolarity increased (OR: 2.119, 95% CI: 1.200–3.741; OR: 7.001, 95% CI: 3.175–15.438).

FIGURE 3
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Figure 3. Associations of serum osmolarity with DR severity, NHANES 2005–2008. (A) Model 1: unadjusted. (B) Model 2: Adjusted for age, sex, and race. (C) Model 3: Adjusted for age, sex, race, education, marital status, BMI, smoke status, alcohol consumption, blood glycohemoglobin, serum total cholesterol, serum albumin, comorbidities, use of diuretics, and ophthalmic imaging status. Mild NPR, mild non-proliferative retinopathy; Moderate/severe NPR, moderate/severe non-proliferative retinopathy; PDR, proliferative retinopathy.

Association between hydration status by calculated osmolarity and DR in older adults

In Figure 4, we sorted hydration status into four groups by calculated osmolarity. Among the 1,834 adults aged 65 years or older, 53.3% of them (n = 978) had normal hydration, 29.7% adults were of impending dehydration (n = 545), 11.0% adults were dehydrated (n = 201), and 6.0% adults were of hyperhydration (n = 110). Similar trends could be seen in Model 1, 2, and 3. After fully adjusting, dehydration was significantly associated with DR (OR: 2.039, 95% CI: 1.305–3.186), whereas impending dehydration or hyperhydration had no significant differences with DR.

FIGURE 4
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Figure 4. Associations of hydration status by calculated osmolarity with DR in older adults, NHANES 2005-2008. (A) Model 1: Unadjusted. (B) Model 2: Adjusted for age, sex, and race. (C) Model 3: Adjusted for age, sex, race, education, marital status, BMI, smoke status, alcohol consumption, blood glycohemoglobin, serum total cholesterol, serum albumin, comorbidities, use of diuretics, and ophthalmic imaging status.

Discussion

From this cross-sectional study based on NHANES 2005–2008, we found the association between hydration status and DR. Participants with higher serum osmolarity were more likely to develop DR and to have more serious DR levels.

When we used serum osmolality, the gold standard currently, to evaluate hydration status in adults, only 0.1% of them were dehydrated. However, 6.8% participants had dehydration by using calculated osmolarity. The explanations for these differences are as follows. Firstly, comorbidities including hyperglycemia, hypertension, and hyperlipidemia might have a greater impact on DR than dehydration. Blood glucose and urea nitrogen levels were more emphasized in calculated osmolarity. It seemed that in diabetic kidney disease patients with albuminuria, glomerular filtration rate and albumin excretion rate were independently associated with DR (37). Secondly, serum osmolality above 300 mOsm/kg was the diagnostic criteria of hypotonic dehydration (15). Salt and water balance should also be taken into account when serum osmolality was at a normal level, as isotonic or hypotonic dehydration might also be existed (38, 39). For patients with mild to moderate dehydration, oral or enteral rehydration and subcutaneous infusion are the main therapy methods (9). Parenteral administration of fluids and electrolytes is the preferred treatment for severe dehydration (40). However, dehydration could be prevented by consuming adequate fluid and keeping the balance of fluids and electrolytes (41, 42). Adequate fluid intake could be achieved by providing straws and cups, offering fluids regularly, using frozen juice bars, and increasing awareness of factors responsible for dehydration such as fever, hot weather, vomiting and diarrhea (9).

The results of this study can be explained by the following mechanisms. Water makes up a quite high proportion of our eyes, with the highest concentrations in aqueous and vitreous humors (about 98–99% by volume) (10, 43). The occurrence and progression of DR is related to complex vascular, inflammatory, and neuronal mechanisms (44). Hydration status played an important role in the pathophysiological process of DR. Madonna, et al. demonstrated that glucose-related hyperosmolarity could promote retinopathy in type 1 diabetic mice (45). Blood-retinal barrier (BRB) was composed of retinal endothelial cells and retinal pigment epithelial (RPE) cells, which played an important role in water and ion balance (46, 47). With the increase of serum osmolarity, the RPE may be affected by hyperosmolar stimulus, resulting in a breakdown of BRB (47, 48). Simultaneously, high serum osmolality influences the function of RPE in eliminating water from subretinal space, resulting in retinal edema (47). In addition, rapid water transport by Müller glial cells may result from dehydration of the outer retina, and this alteration may lead to edema in the post-ischaemic retina (49). Retinal edema is a risk factor of retinal injury especially when the retina is in an inflammatory and ischaemic state (49, 50).

In a real-life pilot study, dehydration caused by prolonged physical effort may alter the retinal structure and its vascularization, leading to a low ocular blood flow rate (51). NPR is caused as a result of altered retinal blood flow and vascular permeability, thickened basement membrane, lost pericytes, and formed acellular capillary (26, 5254). Dehydration also contributed to the up-regulation of interleukin-6 (IL-6) in the supraoptic and paraventricular regions, which lead to an increase in IL-6 secretion (5557). IL-6, a potent angiogenic factor, is significantly associated with DR severity, especially in patients with PDR (5860).

This study has several strengths. To the best of our knowledge, this is the first study to investigate the association between hydration status and DR. We used NHANES data, which contained the nationally representative samples of adult population in United States. We also used serum osmolality, the gold standard, to assess hydration status in order to ensure the accuracy of the results. Moreover, elderly people frequently dehydrate, especially those who reside in care facilities (23, 61). The results of this study remind us of paying closer attention to hydration status, which may help to delay the progress of DR.

The limitations of this study should also be addressed. Firstly, this is a cross-sectional study. Despite there is a significant association between hydration status and DR, the cause-effect relationship is still unclear. Secondly, the proportion of dehydration was low, therefore we divided the data into quartiles to identify different levels of hydration status. As a result, we lacked a judgment criterion for abnormal hydration status, making it challenging to estimate the risk of DR from dehydration in real life. Thirdly, we only considered the most common form—hypertonic dehydration, which could be measured by serum osmolality directly. Isotonic or hypotonic dehydration is hard to diagnose by the currently available data. Moreover, although non-mydriatic digital retinal images are not the gold standard for DR diagnosis, they can be equally used to screen the diabetic population and grade DR severity (62). Finally, because the retinal imaging exam was only performed from 2005 to 2008, the survey data might not be suitable for current conditions.

Conclusions

In conclusion, this study revealed a significant positive association between hydration status and DR. The severity of DR increased as the serum osmolality rose. For people at risk for DR, it is critical to pay close attention to their hydration status in order to prevent and delay the occurrence of vision loss. For diabetics and older adults, adequate fluid intake is essential. Meanwhile, physicians are urged to correct their patients' abnormal hydration status timely. Furthermore, teleophthalmology, an accurate, fast, and affordable method for DR screening, has developed rapidly and may help reduce the burden of deteriorating DR due to the difficulty of monitoring and timely treatment in specialized medical institutions in the future (63, 64).

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

The studies involving human participants were reviewed and approved by the National Center for Health Statistics Research Ethics Review Board. The patients/participants provided their written informed consent to participate in this study.

Author contributions

JZ: conceptualization, data analysis, and writing-original draft. ZR and JL: data curation and validation. JZ, ZR, QZ, RZ, CZ, and JL: revision, editing the manuscript, read, and approved the final manuscript.

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.

References

1. Cheung N, Mitchell P, Wong TY. Diabetic retinopathy. Lancet (London, England). (2010) 376:124–36. doi: 10.1016/s0140-6736(09)62124-3

PubMed Abstract | CrossRef Full Text | Google Scholar

2. Wang W, lo ACY. Diabetic retinopathy: pathophysiology and treatments. Int J Mol Sci. (2018) 19:1816. doi: 10.3390/ijms19061816

PubMed Abstract | CrossRef Full Text | Google Scholar

3. Teo zl, Tham Y-C, Yu M, Chee ML, Rim TH, Cheung N, et al. Global prevalence of diabetic retinopathy and projection of burden through 2045: systematic review and meta-analysis. Ophthalmology. (2021) 128:1580–91. doi: 10.1016/j.ophtha.2021.04.027

PubMed Abstract | CrossRef Full Text | Google Scholar

4. Blindness G, collaborators vi, study vlegotgbod. Causes of blindness and vision impairment in 2020 and trends over 30 years, and prevalence of avoidable blindness in relation to vision 2020: the right to sight: an analysis for the global burden of disease study. Lancet Global Health. (2021) 9:e144–60. doi: 10.1016/s2214–109x(20)30489–7

PubMed Abstract | CrossRef Full Text | Google Scholar

5. Elmadfa I, Meyer AL. Patterns of drinking and eating across the european union: implications for hydration status. Nutr Rev. (2015) 73 (suppl. 2):141–7. doi: 10.1093/nutrit/nuv034

PubMed Abstract | CrossRef Full Text | Google Scholar

6. Lacey J, Corbett J, forni L, Hooper L, Hughes f, Minto G, et al. A multidisciplinary consensus on dehydration: definitions, diagnostic methods and clinical implications. Ann med. (2019) 51:232–51. doi: 10.1080/07853890.2019.1628352

PubMed Abstract | CrossRef Full Text | Google Scholar

7. Rosi IM, Milos R, Cortinovis I, Laquintana D, Bonetti L. Sensitivity and specificity of the new geriatric dehydration screening tool: an observational diagnostic study. Nutrition (burbank, los angeles county, calif). (2022) 101:111695. doi: 10.1016/j.nut.2022.111695

PubMed Abstract | CrossRef Full Text | Google Scholar

8. EL-Sharkawy am, Sahota O, Lobo DN. Acute and chronic effects of hydration status on health. Nutr Rev. (2015) 73 (suppl. 2):97–109. doi: 10.1093/nutrit/nuv038

PubMed Abstract | CrossRef Full Text | Google Scholar

9. Thomas DR, Cote TR, Lawhorne L, Levenson SA, Rubenstein LZ, Smith DA, et al. Understanding clinical dehydration and its treatment. J am Med Direct Assoc. (2008) 9:292–301. doi: 10.1016/j.jamda.2008.03.006

PubMed Abstract | CrossRef Full Text | Google Scholar

10. Sherwin JC, Kokavec J, Thornton SN. Hydration, fluid regulation and the eye: in health and disease. Clin Exp Ophthalmol. (2015) 43:749–64. doi: 10.1111/ceo.12546

PubMed Abstract | CrossRef Full Text | Google Scholar

11. Inan UU, Yücel A, Ermis SS, Oztürk F. The effect of dehydration and fasting on ocular blood flow. J Glaucoma. (2002) 11:411–5. doi: 10.1097/00061198-200210000-00007

PubMed Abstract | CrossRef Full Text | Google Scholar

12. Balk LJ, Sonder JM, Strijbis EMM, Twisk JWR, Killestein J, Uitdehaag BMJ, et al. The physiological variation of the retinal nerve fiber layer thickness and macular volume in humans as assessed by spectral domain-optical coherence tomography. Invest Ophthalmol Visual Sci. (2012) 53:1251–7. doi: 10.1167/iovs.11-8209

PubMed Abstract | CrossRef Full Text | Google Scholar

13. Meng N, Liu J, Zhang Y, Ma J, Li H, Qu Y. Color doppler imaging analysis of retrobulbar blood flow velocities in diabetic patients without or with retinopathy: a meta-analysis. J ultrasound Med : Off J Am Inst ultrasound Med. (2014) 33:1381–9. doi: 10.7863/ultra.33.8.1381

PubMed Abstract | CrossRef Full Text | Google Scholar

14. Shi R, Guo Z, Wang F, Li R, Zhao L, Lin R. Alterations in retinal nerve fiber layer thickness in early stages of diabetic retinopathy and potential risk factors. Curr Eye Res. (2018) 43:244–53. doi: 10.1080/02713683.2017.1387669

PubMed Abstract | CrossRef Full Text | Google Scholar

15. Beck AM, Seemer J, Knudsen AW, Munk T. Narrative review of low-intake dehydration in older adults. Nutrients. (2021) 13:3142. doi: 10.3390/nu13093142

PubMed Abstract | CrossRef Full Text | Google Scholar

16. Munk T, Bech CB, Klausen TW, Rønholt F, Suetta C, Knudsen AW. Accuracy of the calculated serum osmolarity to screen for hyperosmolar dehydration in older hospitalised medical patients. Clin Nutr Espen. (2021) 43:415–9. doi: 10.1016/j.clnesp.2021.03.014

PubMed Abstract | CrossRef Full Text | Google Scholar

17. Bunn DK, Hooper L. Signs and symptoms of low-intake dehydration do not work in older care home residents-drie diagnostic accuracy study. J Am Med Direct Assoc. (2019) 20:963–70. doi: 10.1016/j.jamda.2019.01.122

PubMed Abstract | CrossRef Full Text | Google Scholar

18. Ziegler R, Neu A. Diabetes in childhood and adolescence. Deutsches Arzteblatt Int. (2018) 115:146–56. doi: 10.3238/arztebl.2018.0146

PubMed Abstract | CrossRef Full Text | Google Scholar

19. Shen Y, Cheng X, Ying M, Chang H–T, Zhang W. Association between serum osmolarity and mortality in patients who are critically ill: a retrospective cohort study. Bmj Open. (2017) 7:e015729. doi: 10.1136/bmjopen-2016-015729

PubMed Abstract | CrossRef Full Text | Google Scholar

20. El-Sharkawy AM, Devonald MAJ, Humes DJ, Sahota O, Lobo DN. Hyperosmolar dehydration: a predictor of kidney injury and outcome in hospitalised older adults. Clin Nutr (Edinburgh, Scotland). (2020) 39:2593–9. doi: 10.1016/j.clnu.2019.11.030

PubMed Abstract | CrossRef Full Text | Google Scholar

21. Hooper L, Abdelhamid A, Ali A, Bunn DK, Jennings A, John WG, et al. Diagnostic accuracy of calculated serum osmolarity to predict dehydration in older people: adding value to pathology laboratory reports. Bmj Open. (2015) 5:e008846. doi: 10.1136/bmjopen-2015-008846

PubMed Abstract | CrossRef Full Text | Google Scholar

22. Volkert D, Beck AM, Cederholm T, Cruz-Jentoft A, Hooper L, Kiesswetter E, et al. Espen practical guideline: clinical nutrition and hydration in geriatrics. Clin Nutr (Edinburgh, Scotland). (2022) 41:958–89. doi: 10.1016/j.clnu.2022.01.024

PubMed Abstract | CrossRef Full Text | Google Scholar

23. Siervo M, Bunn D, Prado CM, Hooper L. Accuracy of prediction equations for serum osmolarity in frail older people with and without diabetes. Am J Clin Nutr. (2014) 100:867–76. doi: 10.3945/ajcn.114.086769

PubMed Abstract | CrossRef Full Text | Google Scholar

24. Bethancourt HJ, Kenney WL, Almeida DM, Rosinger AY. Cognitive performance in relation to hydration status and water intake among older adults, nhanes 2011-2014. Eur j Nutr. (2020) 59:3133–48. doi: 10.1007/s00394-019-02152-9

PubMed Abstract | CrossRef Full Text | Google Scholar

25. National health and nutrition examination survey. Nhanes digital grading protocol. Available online at: https://wwwn.cdc.gov/nchs/data/nhanes/2005-2006/manuals/nhanes_ophthamology_digital_grading_protocol.pdf (accessed october 4, 2022).

Google Scholar

26. Antonetti DA, Silva PS, Stitt AW. Current understanding of the molecular and cellular pathology of diabetic retinopathy. Nat Rev Endocrinol. (2021) 17:195–206. doi: 10.1038/s41574-020-00451-4

PubMed Abstract | CrossRef Full Text | Google Scholar

27. Duh EJ, Sun JK, Stitt AW. Diabetic retinopathy: current understanding, mechanisms, and treatment strategies. Jci Insight. (2017) 2:e93751. doi: 10.1172/jci.insight.93751

PubMed Abstract | CrossRef Full Text | Google Scholar

28. Committee ADAPP, Draznin B, Aroda VR, Bakris G, Benson G, Brown FM, et al. 6. Glycemic targets: standards of medical care in diabetes-2022. Diab Care. (2022) 45(suppl. 1):s83–96. doi: 10.2337/dc22-s006

PubMed Abstract | CrossRef Full Text | Google Scholar

29. Grundy SM, Stone NJ, Bailey AL, Beam C, Birtcher KK, Blumenthal RS, et al. 2018 aha/acc/aacvpr/aapa/abc/acpm/ada/ags/apha/aspc/nla/pcna guideline on the management of blood cholesterol: a report of the american college of cardiology/american heart association task force on clinical practice guidelines. Circulation. (2019) 139:e1082–143. doi: 10.1161/cir.0000000000000698

PubMed Abstract | CrossRef Full Text | Google Scholar

30. Zhang J, Deng Y, Wan Y, He S, Cai W, Xu J. Association between serum albumin level and microvascular complications of type 2 diabetes mellitus. Diabetes Metab Syndr Obes. (2022) 15:2173–82. doi: 10.2147/dmso.s373160

PubMed Abstract | CrossRef Full Text | Google Scholar

31. Bringmann A, Hollborn M, Kohen L, Wiedemann P. Intake of dietary salt and drinking water: implications for the development of age-related macular degeneration. Mol Vis. (2016) 22:1437–54.

PubMed Abstract | Google Scholar

32. Whelton PK, Carey RM, Aronow WS, Casey DE, Collins KJ, Himmelfarb CD, et al. 2017 acc/aha/aapa/abc/acpm/ags/apha/ash/aspc/nma/pcna guideline for the prevention, detection, evaluation, and management of high blood pressure in adults: a report of the american college of cardiology/american heart association task force on clinical practice guidelines. J Am Coll Cardiol. (2018) 71:e127–248. doi: 10.1161/hyp.0000000000000076

PubMed Abstract | CrossRef Full Text | Google Scholar

33. Lalama MA, Saloum Y. Nutrition, fluid, and electrolytes in chronic liver disease. Clin Liver Dis. (2016) 7:18–20. doi: 10.1002/cld.526

PubMed Abstract | CrossRef Full Text | Google Scholar

34. Vargas F, Moreno JM, Rodríguez-Gómez I, Wangensteen R, Osuna A, Alvarez-Guerra M, et al. Vascular and renal function in experimental thyroid disorders. Eur J Endocrinol. (2006) 154:197–212. doi: 10.1530/eje.1.02093

PubMed Abstract | CrossRef Full Text | Google Scholar

35. Chrysohoou C, Mantzouranis E, Dimitroglou Y, Mavroudis A, Tsioufis K. Fluid and salt balance and the role of nutrition in heart failure. Nutrients. (2022) 14:1386. doi: 10.3390/nu14071386

PubMed Abstract | CrossRef Full Text | Google Scholar

36. Potter PC, Klein M, Weinberg EG. Hydration in severe acute asthma. Arch Dis Childhood. (1991) 66:216–9. doi: 10.1136/adc.66.2.216

PubMed Abstract | CrossRef Full Text | Google Scholar

37. Sasso FC, Pafundi PC, Gelso A, Bono V, Costagliola C, Marfella R, et al. Relationship between albuminuric ckd and diabetic retinopathy in a real-world setting of type 2 diabetes: findings from no blind study. Nutr Metab Cardiovas Dis : NMCD. (2019) 29:923–30. doi: 10.1016/j.numecd.2019.05.065

PubMed Abstract | CrossRef Full Text | Google Scholar

38. Morley je. Dehydration, hypernatremia, and hyponatremia. Clin Geriatr Med. (2015) 31:389–99. doi: 10.1016/j.cger.2015.04.007

PubMed Abstract | CrossRef Full Text | Google Scholar

39. Reubi FC. Hemodynamic changes in isotonic dehydration. Contrib Nephrol. (1980) 21:55–61. doi: 10.1159/000385247

PubMed Abstract | CrossRef Full Text | Google Scholar

40. Reber E, Gomes F, Dähn IA, Vasiloglou MF, Stanga Z. Management of dehydration in patients suffering swallowing difficulties. J Clin Med. (2019) 8:1923. doi: 10.3390/jcm8111923

PubMed Abstract | CrossRef Full Text | Google Scholar

41. Mentes J. Oral hydration in older adults: greater awareness is needed in preventing, recognizing, and treating dehydration. Am J Nurs. (2006) 106:40–9. doi: 10.1097/00000446-200606000-00023

PubMed Abstract | CrossRef Full Text | Google Scholar

42. Miller HJ. Dehydration in the older adult. J Gerontol Nurs. (2015) 41:8–13. doi: 10.3928/00989134-20150814-02

PubMed Abstract | CrossRef Full Text | Google Scholar

43. Fischbarg J. Water channels and their roles in some ocular tissues. Mol Aspects Med. (2012) 33:638–41. doi: 10.1016/j.mam.2012.07.016

PubMed Abstract | CrossRef Full Text | Google Scholar

44. Semeraro F, Cancarini A, Dell'omo R, Rezzola S, Romano MR, Costagliola C. Diab Ret: Vasc Inflamm Dis J Diab Res. (2015) 2015:582060. doi: 10.1155/2015/582060

PubMed Abstract | CrossRef Full Text | Google Scholar

45. Madonna R, Giovannelli G, Confalone P, Renna FV, Geng Y-J, Caterina RD. High glucose-induced hyperosmolarity contributes to cox-2 expression and angiogenesis: implications for diabetic retinopathy. Cardiovas Diabetol. (2016) 15:18. doi: 10.1186/s12933-016-0342-4

PubMed Abstract | CrossRef Full Text | Google Scholar

46. Jo DH, Yun J-H, Cho CS, Kim JH, Kim JH, Cho C-H. Interaction between microglia and retinal pigment epithelial cells determines the integrity of outer blood-retinal barrier in diabetic retinopathy. Glia. (2019) 67:321–31. doi: 10.1002/glia.23542

PubMed Abstract | CrossRef Full Text | Google Scholar

47. Willermain F, Scifo L, Weber C, Caspers L, Perret J, Delporte C. Potential interplay between hyperosmolarity and inflammation on retinal pigmented epithelium in pathogenesis of diabetic retinopathy. Int J Mol Sci. (2018) 19:1056. doi: 10.3390/ijms19041056

PubMed Abstract | CrossRef Full Text | Google Scholar

48. Orgül S, Reuter U, Kain HL. Osmotic stress in an in vitro model of the outer blood-retinal barrier. Ger J Ophthalmol. (1993) 2:436–43.

PubMed Abstract | Google Scholar

49. Bringmann A, Uckermann O, Pannicke T, Iandiev I, Reichenbach A, Wiedemann P. Neuronal versus glial cell swelling in the ischaemic retina. Acta Ophthalmol Scandinavica. (2005) 83:528–38. doi: 10.1111/j.1600-0420.2005.00565.x

PubMed Abstract | CrossRef Full Text | Google Scholar

50. Daruich A, Matet A, Moulin A, Kowalczuk L, Nicolas M, Sellam A, et al. Mechanisms of macular edema: beyond the surface. Prog Ret Eye Res. (2018) 63:20–68. doi: 10.1016/j.preteyeres.2017.10.006

PubMed Abstract | CrossRef Full Text | Google Scholar

51. Mauget-Faýsse M, Arej N, Paternoster M, Zuber K, Derrien S, Thevenin S, et al. Retinal and choroidal blood flow variations after an endurance exercise: a real-life pilot study at the paris marathon. J Sci Med Sport. (2021) 24:1100–4. doi: 10.1016/j.jsams.2021.03.013

PubMed Abstract | CrossRef Full Text | Google Scholar

52. Kohner EM, Patel V, Rassam SM. Role of blood flow and impaired autoregulation in the pathogenesis of diabetic retinopathy. Diabetes. (1995) 44:603–7. doi: 10.2337/diabetes.44.6.603

PubMed Abstract | CrossRef Full Text | Google Scholar

53. Roy S, Ha J, Trudeau K, Beglova E. Vascular basement membrane thickening in diabetic retinopathy. Curr Eye Res. (2010) 35:1045–56. doi: 10.3109/02713683.2010.514659

PubMed Abstract | CrossRef Full Text | Google Scholar

54. Enge M, Bjarnegård M, Gerhardt H, Hustafsson E, Kalén M, Asker N, et al. Endothelium-specific platelet-derived growth factor-b ablation mimics diabetic retinopathy. Embo J. (2002) 21:4307–16. doi: 10.1093/emboj/cdf418

PubMed Abstract | CrossRef Full Text | Google Scholar

55. Costello JT, Rendell RA, Furber M, Massey HC, Tipton MJ, Young JS, et al. Effects of acute or chronic heat exposure, exercise and dehydration on plasma cortisol, il-6 and crp levels in trained males. Cytokine. (2018) 110:277–83. doi: 10.1016/j.cyto.2018.01.018

PubMed Abstract | CrossRef Full Text | Google Scholar

56. Ghorbel MT, Sharman G, Leroux M, Barrett T, Donovan DM, Becker KG, et al. Microarray analysis reveals interleukin-6 as a novel secretory product of the hypothalamo-neurohypophyseal system. J Biol Chem. (2003) 278:19280–5. doi: 10.1074/jbc.m209902200

PubMed Abstract | CrossRef Full Text | Google Scholar

57. Rubio MFR, Eriksson U, Brummer RJ, König J. Sauna dehydration as a new physiological challenge model for intestinal barrier function. Scient Rep. (2021) 11:15514. doi: 10.1038/s41598-021-94814-0

PubMed Abstract | CrossRef Full Text | Google Scholar

58. Funatsu H, Yamashita H, Noma H, Mimura T, Nakamura S, Sakata K, et al. Aqueous humor levels of cytokines are related to vitreous levels and progression of diabetic retinopathy in diabetic patients. Graefe's Arch Clin Exp Ophthalmol. (2005) 243:3–8. doi: 10.1007/s00417-004-0950-7

PubMed Abstract | CrossRef Full Text | Google Scholar

59. Mocan MC, Kadayifcilar S, Eldem B. Elevated intravitreal interleukin-6 levels in patients with proliferative diabetic retinopathy. Can J Ophthalmol J Can D'Ophtalmol. (2006) 41:747–52. doi: 10.3129/i06-070

PubMed Abstract | CrossRef Full Text | Google Scholar

60. Arjamaa O, Pöllönen M, Kinnunen K, Ryhänen T, Kaarniranta K. Increased il-6 levels are not related to nf-κb or hif-1α transcription factors activity in the vitreous of proliferative diabetic retinopathy. J Diab Compl. (2011) 25:393–7. doi: 10.1016/j.jdiacomp.2011.06.002

PubMed Abstract | CrossRef Full Text | Google Scholar

61. Nagae M, Umegaki H, Onishi J, Huang CH, Yamada Y, Watanabe K, et al. Chronic dehydration in nursing home residents. Nutrients. (2020) 12:3562. doi: 10.3390/nu12113562

PubMed Abstract | CrossRef Full Text | Google Scholar

62. Committee ADAPP, Draznin B, Aroda VR, Bakris G, Benson G, Brown FM, et al. 14 children and adolescents: standards of medical care in diabetes-2022. Diab Care. (2022) 45(suppl. 1):s208–31. doi: 10.2337/dc22-s014

PubMed Abstract | CrossRef Full Text | Google Scholar

63. Sasso FC, Pafundi PC, Gelso A, Bono V, Costagliola C, Marfella R, et al. Telemedicine for screening diabetic retinopathy: the no blind italian multicenter study. Diab/Metabol Res Rev. (2019) 35:e3113. doi: 10.1002/dmrr.3113

PubMed Abstract | CrossRef Full Text | Google Scholar

64. Galiero R, Pafundi PC, Nevola R, Rinaldi L, Acierno C, Caturano A, et al. The importance of telemedicine during covid-19 pandemic: a focus on diabetic retinopathy. J Diab Res. (2020) 2020:9036847. doi: 10.1155/2020/9036847

PubMed Abstract | CrossRef Full Text | Google Scholar

Keywords: hydration, retinopathy, osmolality, dehydration, NHANES

Citation: Zhang J, Ren Z, Zhang Q, Zhang R, Zhang C and Liu J (2022) Lower hydration status increased diabetic retinopathy among middle-aged adults and older adults: Results from NHANES 2005-2008. Front. Public Health 10:1023747. doi: 10.3389/fpubh.2022.1023747

Received: 20 August 2022; Accepted: 10 October 2022;
Published: 26 October 2022.

Edited by:

Ferdinando Carlo Sasso, University of Campania Luigi Vanvitelli, Italy

Reviewed by:

Alfredo Caturano, University of Campania Luigi Vanvitelli, Italy
Raffaele Galiero, Università della Campania Luigi Vanvitelli, Italy

Copyright © 2022 Zhang, Ren, Zhang, Zhang, Zhang and Liu. 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: Chunmei Zhang, bGhncXR6aGFuZyYjeDAwMDQwOzE2My5jb20=; Jufen Liu, bGl1anVmZW4mI3gwMDA0MDtiam11LmVkdS5jbg==

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