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Hypovitaminosis D in Chinese type 2 diabetes: Lack of impact on clinical metabolic status and biomarkers of cellular inflammationThe Diabetes Centre, Royal Prince Alfred Hospital, Sydney, New South Wales, Australia, connie.luo{at}email.cs.nsw.gov.au
The Diabetes Centre, Royal Prince Alfred Hospital, Sydney, New South Wales, Australia, Discipline of Medicine, University of Sydney, Sydney, New South Wales, Australia
Discipline of Medicine, University of Sydney, Sydney, New South Wales, Australia
Discipline of Medicine, University of Sydney, Sydney, New South Wales, Australia
The Diabetes Centre, Royal Prince Alfred Hospital, Sydney, New South Wales, Australia, Discipline of Medicine, University of Sydney, Sydney, New South Wales, Australia
The Diabetes Centre, Royal Prince Alfred Hospital, Sydney, New South Wales, Australia, Discipline of Medicine, University of Sydney, Sydney, New South Wales, Australia Objective: Low vitamin D (25 OH vitamin D) is implicated in the development of diabetes and the metabolic syndrome. We examined whether hypovitaminosis D has a clinically significant impact on glycaemia, metabolic status and inflammatory markers in Chinese patients with established type 2 diabetes.
Methods: Characteristics of 109 patients aged over 50 years were stratified by 25 OH vitamin D status. Patients identified as 25 OH vitamin D deficient (
Results: Vitamin D deficiency was common, affecting 36% of patients. There was no impact of hypovitaminosis D on metabolic syndrome status, HbA1c or insulin use (p Conclusion: There is no relationship between hypovitaminosis D and metabolic control or inflammatory markers in established type 2 diabetes.This suggests that at least in Chinese populations, the effect of low vitamin D is not clinically significant once diabetes is established. Future 25OHVitD intervention trials should therefore focus on prevention in pre-diabetes.
Key Words: diabetes vitamin D metabolic syndrome obesity complications
Diabetes and Vascular Disease Research, Vol. 6, No. 3,
194-199 (2009) |
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50 nmol/L) received cholecalciferol 2,000 IU daily for three months. Measurement of HbA1c, metabolic syndrome parameters, 25 OH vitamin D, calcium, phosphate, PTH, hsCRP and ferritin were taken at baseline and then 25 OH vitamin D, PTH, calcium, phosphate monthly for three months in those on replacement therapy.
0.4 for all) and no association between 25OHVitD and ferritin or hsCRP (p