Association of Vitamin D Deficiency with Diabetic Nephropathy

So-hyeon Hong; Young Bin Kim; Hoon Sung Choi; Tae-Dong Jeong; Jin Taek Kim; Yeon Ah Sung

doi:10.3803/EnM.2020.826

Endocrinol Metab > Volume 36(1); 2021 > Article

Hong, Kim, Choi, Jeong, Kim, and Sung: Association of Vitamin D Deficiency with Diabetic Nephropathy

Original Article

Endocrinology and Metabolism 2021;36(1):106-113.

Published online: February 24, 2021

DOI: https://doi.org/10.3803/EnM.2020.826

Association of Vitamin D Deficiency with Diabetic Nephropathy

So-hyeon Hong¹

, Young Bin Kim², Hoon Sung Choi³, Tae-Dong Jeong⁴, Jin Taek Kim²

, Yeon Ah Sung¹

¹Division of Endocrinology and Metabolism, Department of Internal Medicine, Ewha Womans University School of Medicine, Seoul, Korea

²Department of Internal Medicine, Nowon Eulji Medical Center, Eulji University School of Medicine, Seoul, Korea

³Department of Internal Medicine, Kangwon National University School of Medicine, Chuncheon, Korea

⁴Department of Laboratory Medicine, Ewha Womans University School of Medicine, Seoul, Korea

Corresponding authors: Yeon Ah Sung. Division of Endocrinology and Metabolism, Department of Internal Medicine, Ewha Womans University Medical Center, 1071 Anyangcheon-ro, Yangcheon-gu, Seoul 07985, Korea,
Tel: +82-2-2650-5034, Fax: +82-2-2650-5235, E-mail: yasung@ewha.ac.kr

Jin Taek Kim. Division of Endocrinology and Metabolism, Department of Internal Medicine, Nowon Eulji Medical Center, Eulji University School of Medicine, 68 Hangeulbiseong-ro, Nowon-gu, Seoul 01830, Korea,
Tel: +82-2-970-8456, Fax: +82-2-970-8862, E-mail: jtkimmd@eulji.ac.kr

Received August 27, 2020 Revised December 5, 2020 Accepted December 10, 2020

This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

Background

Low 25-hydroxyvitamin D (25OHD) levels are associated with the incidence of type 2 diabetes mellitus (T2DM). However, the association between 25OHD and metabolic health status or diabetic complications is inconclusive. We evaluated this relationship between vitamin D status and metabolic parameters and complications of T2DM.

Methods

This study included 1,392 patients with T2DM who visited Eulji and Ewha Diabetes Center between January 2011 and August 2016. Anthropometric parameters and laboratory tests including glycated hemoglobin (HbA1c), lipid profile, liver and kidney function, and urinary albumin-to-creatinine ratio (UACR) were evaluated. Diabetic macro- and microvascular complications were determined through a medical record review. Serum 25OHD concentrations were measured by chemiluminescent immunoassay.

Results

The mean 25OHD level was 16.8±9.6 ng/mL. Vitamin D deficiency (<20 ng/mL) and severe deficiency (<10 ng/mL) were observed in 990 (71.1%) and 351 (25.2%) participants, respectively. 25OHD level was positively correlated with age and high-density lipoprotein cholesterol (HDL-C) level and negatively correlated with HbA1c, triglyceride level, and UACR. HDL-C and UACR were significantly associated with 25OHD after adjusting for other variables. Vitamin D deficiency was independently related to nephropathy after adjusting for confounding variables.

Conclusion

Vitamin D deficiency was common among Korean T2DM patients; it was independently associated with microalbuminuria and HDL level, and positively related to diabetic nephropathy.

Keywords: Albuminuria; Diabetes complications; Diabetic nephropathies; Vitamin D

INTRODUCTION

Vitamin D, traditionally known for its role in regulating bone and calcium metabolism, has recently been implicated in a multitude of systems including the cardiovascular, immune, and reproductive systems [1,2]. The ubiquitous expression of vitamin D receptors in the human body is closely related to these findings, suggesting that vitamin D plays an important role in the regulation of the expression of multiple genes beyond those involved in calcium metabolism [3].

Several large epidemiologic studies on the impact of vitamin D on metabolic and cardiovascular diseases demonstrated that lower vitamin D levels were associated with the incidence of type 2 diabetes mellitus (T2DM) [4,5]. Vitamin D deficiency reportedly reduced intracellular calcium levels and decreased insulin secretion in pancreatic beta cells [6]. Vitamin D deficiency also decreases the insulin receptor expression, leading to peripheral insulin resistance [7]. Furthermore, vitamin D deficiency has an atherosclerotic action, promoting myocardial hypertrophy and renin activation [8].

Vitamin D deficiency is prevalent in South Korea. The 2006 to 2008 Korea National Health and Nutrition Examination Survey (KNHANES), which included adults aged 19 years or older, reported vitamin D deficiency in 47.3% of men and 64.5% of women [9]. Another international study reported that Korean postmenopausal osteoporotic women had the lowest 25-hydroxyvitamin D (25OHD) levels among 18 countries [10]. These findings suggest that vitamin D deficiency may be even more prevalent in T2DM patients in Korea and related to poor glycemic control and/or various complications of T2DM.

However, studies on the association between vitamin D deficiency and micro- and macrovascular complications in T2DM showed conflicting results and are currently inconclusive. Several studies reported that vitamin D deficiency increased the risk of diabetic polyneuropathy [11], nephropathy, and retinopathy [12]. However, other studies found no association between vitamin D deficiency and diabetic polyneuropathy [13] or retinopathy [14]. While vitamin D deficiency was reportedly associated with a lower low-density lipoprotein cholesterol (LDL-C) level and a higher triglyceride level and diastolic blood pressure than those in T2DM patients with sufficient vitamin D level [15], other studies reported no relationship [16].

The present study investigated the prevalence of vitamin D deficiency in Korean patients with T2DM and identified the relationship between vitamin D status and diabetes-related parameters such as glycemic control, macro- and microvascular complications, and cardiovascular risk factors.

METHODS

Study population

This cross-sectional study included 1,564 T2DM patients who visited Eulji Diabetes Center and Ewha Womans University Mokdong Hospital between January 2011 and August 2016. T2DM was diagnosed according to the American Diabetes Association criteria [17]. We excluded patients who took calcium or vitamin D supplements, and patients with diagnosed osteoporosis, chronic kidney stage 5 (estimated glomerular filtration rate [eGFR] <15 mL/min/1.73 m²), liver cirrhosis, or refractory malignancy. Finally, 1,392 patients were included in the analysis. The Institutional Review Boards of the hospitals approved the study (EMCIRB 09-007 and EUMC 2016-07-013-002), and due to a retrospective nature of the study, informed consent was waived.

Anthropometric and biochemical measurements

We collected information on age, sex, smoking status, alcohol consumption, duration of diabetes, and types of diabetic medication used from patient medical records. Height and weight were measured, and body mass index (BMI) was calculated by dividing the weight in kilograms by the height squared in meters. The blood pressure was calculated as the mean of two manual sphygmomanometer readings with the patient in a seated position.

A venous blood sample was collected after an overnight fast for at least 8 hours. 25OHD levels were measured using a chemiluminescent immunoassay (Roche ELECSYS^®, Total Vitamin D, Roche Diagnostics, Mannheim, Germany; and Liaison^® 25-OH Vitamin D Total, DiaSorin, Saluggia, Italy). According to the World Health Organization definitions, vitamin D status was defined as following: severely deficient for 25OHD <10 ng/mL, deficient for 10 ng/mL≤ 25OHD <20 ng/mL, insufficient for 20 ng/mL≤ 25OHD <30 ng/mL, and sufficient for 25OHD ≥30 ng/mL [18].

Glycated hemoglobin (HbA1c) was measured by high-performance liquid chromatography using HLC-723G7 and G8 instruments (Tosoh, Tokyo, Japan). Total cholesterol, LDL-C, high-density lipoprotein cholesterol (HDL-C), triglyceride, and creatinine levels were measured using enzymatic colorimetric procedures with an automated analyzer (Hitachi-747, Hitachi, Tokyo, Japan). Total calcium and phosphorus were measured using CA-HR2 and P-HR2 (Wako Pure Chemical Industries, Osaka, Japan), respectively. The eGFR was calculated using the following Modification of Diet in Renal Disease equation: 186×(serum creatinine)^−1.154×(age)^−0.203×(0.742 if female) [19]. The urinary albumin-to-creatinine ratio (UACR) was assessed on a random spot urine sample and measured using radioimmunoassay (Immunotech, Prague, Czech Republic).

Assessment of diabetic complications

The presence of diabetic retinopathy, nephropathy, neuropathy, and cardio and cerebrovascular diseases (CVDs) were investigated through medical record reviews. Diabetic retinopathy was defined as either a non-proliferative or proliferative diabetic retinopathy or previous laser photocoagulation therapy. Diabetic nephropathy was defined as microalbuminuria (UACR 30 to 299 mg/g) or macroalbuminuria (UACR ≥300 mg/g). Diabetic neuropathy was identified in patients by the current perception threshold test (CPT) using a Neurometer (Neurotron Inc., Baltimore, MD, USA) or reported pain, burning, tingling, or numb sensation on the feet or hands. CVD included myocardial infarction, unstable angina, or stroke.

Statistical analysis

The statistical analysis was performed using IBM SPSS Statistics for Windows version 20.0 (IBM Corp., Armonk, NY, USA). Quantitative variables were reported as means and standard deviations and categorical parameters were reported as numbers and percentages. Student’s t test and chi-square test were used for comparisons between groups with continuous and categorical variables, respectively.

The 25OHD levels showed significant seasonal variance, with a significantly lower level during the winter season compared to those in the spring, summer, and autumn after Bonferroni correction (14.4±9.5, 18.2±10.8, 17.1±8.8, and 17.7±9.1 ng/mL, respectively, P for trend <0.01). Therefore, we also adjusted for seasonal variation to winter (from December to February) versus non-winter (from March to November).

Pearson’s correlation tests were used to evaluate the relationships between 25OHD level and diabetes-related clinical and biochemical parameters. Multiple linear regression analysis was performed using the 25OHD levels as independent variables and HbA1c, eGFR, total, LDL-C, and HDL-C, triglycerides, and UACR as dependent variables to determine the relationships between 25OHD levels and diabetes-related factors. Multiple logistic regression was performed to identify the independent association between vitamin D deficiency and macro- and microvascular complications. Two-tailed P values <0.05 were considered statistically significant.

RESULTS

Basal characteristics

The mean age of the participants was 61.6±10.9 years, 57.9% were men, and the mean BMI was 25.8±3.6 kg/m². The mean HbA1c was 7.4%±1.3%, the mean duration of diabetes was 13.0±8.0 years, and 18.5% of patients used insulin. Retinopathy, nephropathy, neuropathy, and CVD were present in 30.3%, 31.2%, 17.2%, and 15.6% of patients, respectively (Supplemental Table S1).

The mean 25OHD level was 16.8±9.6 ng/mL. Overall, only 144 patients (10.3%) showed sufficient 25OHD levels; 351 patients (25.2%) had severe deficiency (<10 ng/mL), 639 patients (45.9%) had 25OHD levels of 10≤ and <20 ng/mL, and 258 patients (18.5%) had values of 20≤ and <30 ng/mL (Supplemental Table S2).

The clinical and metabolic characteristics of the participants stratified by vitamin D deficiency status are presented in Table 1. Among patients with T2DM, those with vitamin D deficiency were younger (60.9 years vs. 63.3 years, P<0.01) and had higher HbA1c (7.5% vs. 7.2%, P<0.01), lower HDL-C (47.3 mg/dL vs. 50.7 mg/dL, P<0.01), and higher triglyceride (164.2 mg/dL vs. 148.7 mg/dL, P=0.01) levels as well as higher UACR (129.1 mg/g vs. 50.6 mg/g, P<0.01) compared to those in participants without vitamin D deficiency. While a higher percentage of vitamin D-deficient participants used insulin (20.4% vs. 13.7%, P<0.01), the duration of diabetes did not differ between the two groups. Additionally, nephropathy was more prevalent in patients with a vitamin D deficiency than in in patients without a vitamin D deficiency (34.0% vs. 24.3%, P<0.01). Other complications did not differ between the two groups.

Correlations between 25OHD levels and clinical and biochemical variables

We observed a significant positive correlation between 25OHD level and age (r=0.05, P=0.045) and HDL-C (r=0.12, P<0.01) and negative associations between 25OHD and HbA1c (r= −0.09, P<0.01), triglycerides (r=-0.08, P<0.01), and UACR (r=-0.13, P<0.01) (Table 2).

Association between 25OHD and diabetes-related clinical and biochemical variables

Correlation analysis through multiple linear regression was performed to identify biochemical variables associated with 25OHD levels. The 25OHD level was positively associated with HDL-C (β=5.56; 95% confidence interval [CI], 1.32 to 9.81; P=0.01) and negatively associated with UACR (β=-194; 95% CI, −290 to −98.0; P<0.01) after adjusting for age, sex, systolic blood pressure, HbA1c, total calcium, phosphorus, duration of diabetes, type of medication, and season (Table 3).

Association between vitamin D deficiency and macro- and microvascular complications

Using the vitamin D insufficiency and sufficiency groups as a reference, the vitamin D deficiency group showed an increased risk of nephropathy after adjusting for age, sex, systolic blood pressure, HbA1c, total calcium, phosphorus, duration of diabetes, type of medication, and season (odds ratio, 1.62; 95% CI, 1.21 to 2.16; P<0.01) (Table 4). Retinopathy, neuropathy, and CVD were not related to vitamin D deficiency.

DISCUSSION

In this study, the 25OHD levels in T2DM patients were correlated with several clinical parameters of diabetes, including HbA1c, albuminuria, triglyceride, and HDL. Among diabetic macro- and microvascular complications, diabetic nephropathy was correlated with the 25OHD level. In particular, the 25OHD level remained an independent risk factor for diabetic nephropathy after adjusting for the other risk factors.

In our study, the rate of vitamin D deficiency (defined as less than 20 ng/mL) was 71.1%, while that for severe deficiency (less than 10 ng/mL) was 25.2%. This prevalence was higher than that in the 2006 to 2008 KNHANES, in which 47.3% and 64.5% of the included adult male and female patients aged 19 years, respectively, were vitamin D-deficient [9]. Vitamin D level was affected by age, obesity, sun exposure, and even diabetes itself; in comparison to that in the KNHANES, our study population was older and more obese and had a longer duration of diabetes. A previous study including 9,524 patients with T2DM aged 50 to 75 years in Australia, New Zealand, and Finland reported vitamin D deficiency in 47.9% of the population [20]. In Asia, two Korean studies reported rates of 18.9% to 54% [13,21], a Japanese study reported a rate of 70.6% [22], and a Chinese study reported a rate of 34.3% [23]. Additionally, another study on Asians living in the UK reported an 83% prevalence of vitamin D deficiency among T2DM patients [24]. The broad ranges of vitamin D status among the studies may be attributed to differences in ethnicity, geography, season, sun exposure, physical activity, age, and glycemic control status.

In the present study, 25OHD level was negatively associated with UACR, and vitamin D deficiency was significantly associated with diabetic nephropathy after adjusting for multidirectional variable parameters including age, sex, systolic blood pressure, duration of diabetes, type of medication, total calcium, phosphorus, HbA1c, and season comparable to the findings of a previous study reporting that vitamin D deficiency increased the risk of diabetic nephropathy progression [25]. An in vitro study showed that vitamin D has a protective effect in the kidneys by reducing levels of transforming growth factor-β and SMAD3 proteins, which are involved in renal fibrosis and oxidative stress [26]. In an animal study, diabetic vitamin D receptor knockout mice developed severe albuminuria compared to diabetic wild-type mice [27]. A clinical study reported that 2 μg/day supplementation of paricalcitol reduced microalbuminuria in patients with diabetic nephropathy [28]. Taken together, these findings demonstrate the negative effects of vitamin D deficiency on albuminuria and diabetic nephropathy. However, we found no association between the 25OHD level and retinopathy or neuropathy in the present study. Several studies have demonstrated the association between vitamin D deficiency and diabetic retinopathy [29,30], while others found no relationship [14,31]. In the case of neuropathy, the data suggest that vitamin D deficiency was associated with neuropathy [32-34]. We did not perform identical methods or use the same diagnostic tools to detect diabetic neuropathy in all patients, which might have increased the false-negative rates; i.e., patients with diabetic neuropathy who did not undergo vibration perception threshold examination nor report abnormal sensations in their feet or hands who could have been considered non-neuropathic patients.

We found that vitamin D deficiency was associated with hypertriglyceridemia and low HDL level and that HDL remained statistically significant after adjusting for other variables. These results are in line with those of previous large-scale general population studies reporting an association between lower vitamin D levels and higher triglyceride and lower HDL levels [35,36]. Another study reported that vitamin D level was positively associated with lipoprotein lipase activity, which acted as a triglyceride hydrolase and bridging factor for receptor-mediated lipoprotein uptake [37]. A study on macrophages extracted from obese, hypertensive T2DM patients showed that activated vitamin D signaling prevented foam cell formation in the macrophages, which is an early sign of atherosclerosis [38]. Together, these observations indicate an association between a lower vitamin D level and unfavorable lipid profiles. However, a previous study of T2DM patients reported insignificant results; the relationship between vitamin D concentration and triglycerides and/or HDL levels disappeared after adjusting for BMI or waist circumference [16]. One possible explanation is that patients with T2DM have ameliorated lipid metabolism compared to that in the general population, which overwhelms the effect of vitamin D on lipid profiles. Another possibility is that even though we did not consider the number of patients taking statins or fibrates, most patients are prescribed individualized doses or types of lipid-lowering agents to reach lipid targets. The average triglyceride and LDL-C levels in the present study were 160 and 92.4 mg/dL, respectively, indicating that these levels nearly optimal.

The strengths of our study include the large study population and the statistically adjustment for seasonal variations. Although we did not measure parathyroid hormone levels, we did adjust for both calcium and phosphorus levels, which are closely related to vitamin D and the parathyroid hormone. The limitations were that we were unable to determine the physical activity and medications status other than that for diabetes, such as renin-angiotensin blocker of the patients. Furthermore, we could not fully account for neuropathy since we relied on medical records for patients’ subjective reports and CPTs conducted before study initiation. Lastly, the cross-sectional design makes it difficult to establish causality.

In conclusion, vitamin D deficiency was highly prevalent among Korean patients with T2DM and was independently associated with increased diabetic nephropathy. Additionally, low vitamin D levels were related to higher triglyceride and lower HDL-C levels in T2DM patients. Additional prospective studies are needed to evaluate the effect of vitamin D on lipid metabolism and diabetic complications.

Supplementary Information

Supplemental Table S1.

Baseline Characteristics of Study Participants (n=1,392)

enm-2020-826-suppl1.pdf

Supplemental Table S2.

Distribution of Serum 25OHD Concentration

enm-2020-826-suppl2.pdf

NOTES

CONFLICTS OF INTEREST

No potential conflict of interest relevant to this article was reported.

AUTHOR CONTRIBUTIONS

Conception or design: S.H., J.T.K., Y.A.S. Acquisition, analysis, or interpretation of data: S.H., Y.B.K., H.S.C., T.D.J., J.T.K., Y.A.S. Drafting the work or revising: S.H., J.T.K., Y.A.S. Final approval of the manuscript: S.H., Y.B.K., H.S.C., T.D.J., J.T.K., Y.A.S.

Table 1

Baseline Characteristics According to Vitamin D Deficiency Status

Characteristic	25OHD <20 ng/mL (n=990)	25OHD ≥20 ng/mL (n=402)	P value
Age, yr	60.9±11.1	63.3±10.2	<0.01

Male, sex	566 (57.2)	240 (59.7)	0.40

BMI, kg/m²	25.9±3.6	25.6±3.6	0.17

SBP, mm Hg	133±16	132±15	0.17

DBP, mm Hg	78±11	77±10	0.10

Smoking status (n=1,246) (former or current)	355 (39.7)	153 (43.5)	0.23

Alcohol status (n=1,248) (yes)	355 (39.7)	178 (50.4)	<0.01

HbA1c, %	7.5±1.4	7.2±1.1	<0.01

Total cholesterol, mg/dL	166±37	168±35	0.45

LDL-C, mg/dL	92.2±29.2	92.8±29.1	0.71

HDL-C, mg/dL	47.3±12.0	50.7±11.8	<0.01

Triglycerides, mg/dL	164.2±109.5	148.7±86.4	0.01

AST, IU/L	25.7±14.4	27.2±23.1	0.15

ALT, IU/L	27.0±19.4	26.6±21.4	0.71

Creatinine, mg/dL	1.03±0.29	1.01±0.21	0.23

eGFR (MDRD), mL/min/1.73 m²	69.8±17.8	69.4±15.1	0.68

UACR, mg/g	129.1±481.0	50.6±148.9	<0.01

Total calcium, mg/dL	9.0±0.5	8.9±0.6	0.02

Phosphorus, mg/dL	3.5±0.8	3.6±0.8	0.32

Duration of diabetes, yr	12.8±8.1	13.6±7.9	0.10

Medication (any insulin)	201 (20.4)	55 (13.7)	<0.01

Complication
Retinopathy (n=931)	214/690 (31.0)	68/241 (28.2)	0.46
Neuropathy (n=1,367)	173/974 (17.8)	62/393 (28.7)	0.43
Nephropathy (n=1,354)	329/967 (34.0)	94/387 (24.3)	<0.01
Cardiovascular disease	158 (16.0)	59 (14.7)	0.57

Values are expressed as mean±standard deviation or number (%).

25OHD, 25-hydroxyvitamin D; BMI, body mass index; SBP, systolic blood pressure; DBP, diastolic blood pressure; HbA1c, glycated hemoglobin; LDL-C, low-density lipoprotein cholesterol; HDL-C, high-density lipoprotein cholesterol; AST, aspartate aminotransferase; ALT, alanine transaminase; eGFR, estimated glomerular filtration rate; MDRD, Modification of Diet in Renal Disease; UACR, urinary albumin-to-creatinine ratio.

Table 2

Correlation Analysis of 25OHD with Clinical and Biochemical Factors

Variable	r	P value
Age	0.05	0.045
BMI	−0.04	0.13
SBP	−0.04	0.15
DBP	−0.05	0.06
HbA1c	−0.09	<0.01
Total cholesterol	−0.02	0.53
LDL-C	−0.02	0.49
HDL-C	0.12	<0.01
Triglycerides	−0.08	<0.01
AST	0.03	0.29
ALT	0.01	0.66
eGFR (MDRD)	0.05	0.09
UACR	−0.13	<0.01
Total calcium	−0.23	0.40
Phosphorus	−0.02	0.48
Duration of diabetes	0.05	0.07

25OHD and triglyceride levels were computed from log-scale.

Table 3

Multiple Linear Regression Analysis of the Associations between 25OHD Concentration and Clinical and Biochemical Variables of Diabetes

Variable	Model 1			Model 2

	β	95% CI	P value	β	95% CI	P value
HbA1c	−0.48	−0.76 to −0.19	<0.01

Total cholesterol	−0.97	−8.51 to 6.57	0.80	5.56	−2.31 to 13.43	0.17

LDL-C	−1.16	−7.43 to 5.12	0.72	0.01	−6.63 to 6.66	0.99

HDL-C	5.88	2.17 to 9.60	<0.01	5.56	1.32 to 9.81	0.01

Triglycerides	−0.09	−0.15 to −0.04	<0.01	−0.04	−0.09 to 0.01	0.12

eGFR	4.48	1.11 to 7.85	0.01	1.82	−1.27 to 4.90	0.25

UACR	−225	−314 to −136	<0.01	−194	−290 to −98.0	<0.01

Model 1: Adjusted for age; Model 2: Adjusted for age, sex, body mass index, systolic blood pressure, HbA1c, total calcium, phosphorus, duration of diabetes, type of medication, and season. 25OHD and triglyceride levels were computed from log-scale.

25OHD, 25-hydroxyvitamin D; CI, confidence interval; HbA1c, glycated hemoglobin; LDL-C, low-density lipoprotein cholesterol; HDL-C, high-density lipoprotein cholesterol; eGFR, estimated glomerular filtration rate; UACR, urinary albumin-to-creatinine ratio.

Table 4

Logistic Regression Analysis of the Association between Vitamin D Deficiency and Diabetic Complications

Variable	Model 1			Model 2

	OR	95% CI	P value	OR	95% CI	P value
Retinopathy	1.17	0.85-1.62	0.34	1.30	0.90-1.88	0.16

Nephropathy	1.72	1.31-2.26	<0.01	1.62	1.21-2.16	<0.01

Neuropathy	1.21	0.88-1.67	0.24	1.31	0.93-1.84	0.12

Cardiovascular disease	1.20	0.86-1.66	0.28	1.22	0.87-1.72	0.26

Model 1: Adjusted for age; Model 2: Adjusted for age, sex, body mass index, systolic blood pressure, glycated hemoglobin, total calcium, phosphorus, duration of diabetes, type of medication, and season.

OR, odds ratio; CI, confidence interval.

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