Polymorphisms in GC and NADSYN1 Genes are associated with vitamin D status and metabolic profile in Non-diabetic adults

BMC Endocrine Disorders - Tập 13 - Trang 1-8 - 2013
Lydia Foucan1,2,3, Fritz-Line Vélayoudom-Céphise1,4, Laurent Larifla1, Christophe Armand1, Jacqueline Deloumeaux1, Cedric Fagour1, Jean Plumasseau5, Marie-Line Portlis6, Longjian Liu7, Fabrice Bonnet8, Jacques Ducros9
1Research group Clinical Epidemiology and MedicineResearch group, University of Antilles and Guyane, Guyane, France
2Department of Public Health and Medical Information, University Hospital of Pointe-à-Pitre, Guadeloupe, France
3Département de Santé Publique, CHU de Pointe-à-Pitre, Pointe-à-Pitre, France
4Diabetology Unit, University Hospital of Pointe-à-Pitre, Guadeloupe, France
5Health Centre, AGREXAM, Les Abymes, France
6Clinical Genetic Unit, University Hospital of Pointe-à-Pitre, Guadeloupe, France
7Department of Epidemiology and Biostatistics, Drexel University School of Public Health, Philadelphia, USA
8Endocrinology-Diabetology and nutrition Unit, University Hospital South of Rennes, Rennes, France
9Nephrology Unit, University Hospital of Pointe-à-Pitre, Guadeloupe, France

Tóm tắt

Our aim was to assess the associations between vitamin D (vitD) status, metabolic profile and polymorphisms in genes involved in the transport (Group-Component: GC) and the hydroxylation (NAD synthetase 1: NADSYN1) of 25 hydroxyvitamin D (25(OH)D) in non-diabetic individuals. We conducted a cross-sectional study with 323 individuals recruited from the Health Center of Guadeloupe, France. The rs2282679 T > G and rs2298849 T > C in GC and rs12785878 G > T in NADSYN1 were genotyped. Mean age was 46(range 18–86) years. 57% of participants had vitD insufficiency, 8% had vitD deficiency, 61% were overweight and 58% had dyslipidemia. A higher frequency of overweight was noted in women carrying rs2298849T allele v CC carriers (71% v 50%; P = 0.035). The rs2282679G allele was associated with increased risks of vitD deficiency and vitD insufficiency (OR =3.53, P = 0.008, OR = 2.34, P = 0.02 respectively). The rs2298849 TT genotype was associated with vitD deficiency and overweight (OR =3.4, P = 0.004 and OR = 1.76, P = 0.04 respectively) and the rs12785878 GG genotype with vitD insufficiency and dyslipidemia (OR = 1.80, P = 0.01 and OR = 1.72, P = 0.03 respectively). Based on the number of risk alleles for rs2282679 and rs12785878 combined, a genotype score of 3 (vs. 0–1) was associated with a 5.5 ng/mL average reduction in serum 25(OH)D levels (P = 0.001). The GC and NADSYN1 genes are associated with the vitamin D status and might contribute to dyslipidemia and overweight independently of 25(OH)D levels.

Tài liệu tham khảo

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