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Study type | Subject division | Population | Vitamin D assessment/supplement | Duration | Conclusion | Citation |
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Cross-sectional | Non-DM T2DM patients | 100 698 | | Vitamin D assessment & main cardiovascular risk factors | — | Prevalence of hypovitaminosis D was higher in diabetic patients with HbA1C, BMI, LDL, and triglycerides than Vitamin D counterparts. 25(OH)D may have an indirect effect mediated by cardiovascular risk factors on CHD | [63] |
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Cross-sectional | Controls Case, diabetic retinopathy | 110 94 | Chinese | Vitamin D receptor gene polymorphism investigated | — | Diabetes duration, systolic blood pressure, HbA1c, and the rs2228570 T allele were associated with increased risk of diabetic retinopathy | [50] |
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Prospective case-control | Control Case (deficient/insufficient serum 25(OH)D3) | 30 31 | China | Vitamin D supplement: case, calcitriol 0.25 μg/daily Control, no dose | 6 months | No effect on FBG, HbA1c, and AUCC-peptide, but reduced blood pressure, inflammation markers, and proteinuria levels after 6 months from baseline | [43] |
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Case-cohort | Control (non-GDM) Case (GDM) | 517 135 | | Vitamin D assessment | | Early pregnancy Vitamin D status was found to be inversely associated with GDM | [33] |
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Prospective cohort | White Black | 8120 2102 | Diverse | Vitamin D assessment | 8 years | Risk association in Blacks No association in Whites | [23] |
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Case-control | Control Case, supplemented | 68 69 | India | Dose administration: 60,000 IU weekly for 4 weeks and then monthly | 1 year | Reduced HbA1c levels, FPG, and 2-h plasma glucose | [28] |
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Randomized double blind | Control Subjects (DM patients) | 21 21 | Tehran | Dose administration: intramuscular injection 300000 IU of Vitamin D3 | 3 months | Dose of Vitamin D improved plasma level but had no effect on HbA1c | [27] |
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Randomized double blind | Placebo Case, T2DM Vitamin D supplemented | 42 45 | UAE | Vitamin D supplementation: phase 1 6000 IU Vitamin D3/day (3 months), phase 2 with 3000 IU Vitamin D3/day, and phase 3 both the arms unblinded and supplemented with 2200 IU Vitamin D3/day for 6 months | 1 year | No significant influence on weight, fat mass, or waist circumference. Target levels of S-25(OH)D above 75 nmol/L in this population were not achievable | [25] |
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Randomized prospective | T1DM male (62%) Female (38%) | 25 | 62% Hispanics | Vitamin D3 (20 000 IU/week) for 6 months, either immediately or after 6 months of observation | 1 year | Did not affect glycaemia or markers of inflammation | [21] |
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Cross-sectional | Female Male | 697 769 | Korean | Vitamin D assessment | — | Significantly decreasing trends for fasting insulin, HOMA-IR, and IFG with increasing 25(OH)D (independent of adiposity) | [18] |
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Prospective case-control | Control Case (diagnosed DM) | 102 102 | India | Vitamin D assessment | 2 years | Controls and cases were deficient in Vitamin D, but it was significantly lower in DM patients. Significant negative correlation between 25(OH)D and HbA1c was observed | [15] |
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