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Apolipoprotein M promoter polymorphisms alter promoter activity and confer the susceptibility to the development of type 1 diabetes
Authors:Xiaopan Wu  Nifang Niu  Kerstin Brismar  Xilin Zhu  Xin Wang  Suad Efendic  Te Du  Yang Liu  Harvest F Gu  Ying Liu
Institution:1. Department of Clinical Biochemistry, Rigshospitalet, University of Copenhagen, Denmark;2. Department of Biomedical Science, University of Copenhagen, Denmark;3. KineMed, Inc., Emeryville, CA, USA;1. Service of Endocrinology and Nutrition, Hospital Clínico Universitario de Valencia, Valencia, Spain;2. CIBER de Diabetes y Enfermedades Metabólicas asociadas (CIBERDEM), Barcelona, Spain;3. Laboratorio de Estudios Genéticos, Fundación para la Investigación. Instituto de Investigación INCLIVA, Valencia, Spain;4. Department of Medicine, University of Valencia, Valencia, Spain;5. Department of Biochemistry and Molecular Biology, University of Valencia and CIBER de Obesidad, Spain
Abstract:ObjectivesApolipoprotein M plays an important role in the formation of preβ-HDL and cholesterol efflux to HDL. In the present study, we investigate the potential association between the ApoM promoter polymorphisms and type 1 diabetes.Design and methodsThe study was conducted in Peking Union Medical College, Beijing, China and Karolinska Institutet, Stockholm, Sweden. Two populations, including 493 Han Chinese subjects (177 T1D patients/316 controls) and 225 Swedish (124/101), are enrolled in the present study. Three single nucleotide polymorphisms (SNP) C-1065A, T-855C and T-778C in the promoter region of the ApoM gene are genotyped using a polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) protocol. Promoter activity was measured by reporter gene assay.ResultsSNP T-778C was strongly associated with T1D in both Han Chinese (p = 0.002, OR = 2.188, CI 95% = 1.338–3.581) and Swedish (p = 0.021, OR = 2.865, CI 95% = 1.128–7.278) populations. The luciferase activity of ?778C promoter was 1.41 times as high as that of ?778T promoter (9.90 ± 1.92 vs. 7.04 ± 0.76, p = 0.001).ConclusionsAllele C of SNP T-778C may increase promoter activity and confer the risk susceptibility to the development of T1D.
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