Background: Diabetes is one of the common chronic diseases in which susceptibility is determined by a combination of genetic and environmental factors, and more than 90% of diabetic patients are diabetes mellitus type 2 (T2DM). The existing studies on the association between CDKAL1 rs10946398 gene polymorphism and susceptibility to type 2 diabetes are inconsistent across populations.
Aim: We aim to explore the association between CDKAL1 rs10946398 gene polymorphism and susceptibility to type 2 diabetes in different populations.
Methods: We examined all studies before June 12, 2021, that associated CDKAL1 rs10946398 with T2DM. Heterogeneity was assessed by meta-analysis of allelic inheritance models (A vs. C), dominant inheritance models (AA vs. AC+CC), and recessive inheritance model (AA+AC vs. CC); was used to assess the heterogeneity (if < 50%, the fixed-effects model was used; if ≥ 50%, the random-effects model was used for data consolidation); correlation was judged by a forest map; potential publication bias was tested by the Egger test ( > 0.05 indicates that there is no publication bias).
Results: Fourteen data totaling 30288 subjects, including 19272 controls and 11016 patients with T2DM, met our inclusion criteria. In the Asian population, the differences were statistically significant ( < 0.01) for dominant genetic model (OR = 0.75, 95%CI = 0.64-0.88, = 0.0003). But the allelic effect model (OR = 0.87, 95%CI = 0.75-1.02, = 0.08) and the recessive genetic model (OR = 0.85, 95%CI = 0.66-1.10, = 0.23) were not statistically significant ( > 0.01). In the non-Asian population, the differences were statistically significant ( < 0.01) for the allelic effect model (OR = 0.83, 95%CI = 0.77-0.88, < 0.00001), the dominant model (OR = 0.79, 95%CI = 0.72-0.87, < 0.00001), and the recessive model (OR = 0.78, 95%CI = 0.70-0.87, < 0.0001).
Conclusion: In this study, CDKAL1 RS10946398 was positively associated with T2DM, but the association was different in Asian populations.
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http://dx.doi.org/10.1155/2021/1254968 | DOI Listing |
Genes (Basel)
August 2023
Department of Physiology, Pomeranian Medical University, 70-204 Szczecin, Poland.
Post-transplant diabetes mellitus (PTDM) is a common complication that occurs in kidney transplant patients, increasing the risk of infection, cardiovascular disease and loss of graft function. Currently, factors that increase the risk of this complication are being sought, among them polymorphisms in genes that regulate carbohydrate metabolism and influence pancreatic β-cell function. The aim of this study was to evaluate the association of selected polymorphisms of genes affecting carbohydrate metabolism, such as rs10946398, rs1799884, rs780094 and rs2191349, with the development of post-transplant diabetes in kidney transplant patients.
View Article and Find Full Text PDFBMJ Open Diabetes Res Care
April 2023
Research Center for Health Promotion in Women, Youth and Children, Hubei Province Key Laboratory of Occupational Hazard Identification and Control, School of Public Health, Wuhan University of Science and Technology, Wuhan, Hubei, china
Introduction: To identify the association of the cyclin-dependent kinase 5 regulatory subunit associated protein 1-like 1 () gene polymorphism with gestational diabetes mellitus (GDM) in the Chinese population.
Research Design And Methods: This case-control study enrolled 835 pregnant women with GDM and 870 pregnant women without diabetes who underwent antenatal examination during 24 to 28 gestational weeks at the Maternal and Child Health Hospital of Hubei Province from January 15, 2018 to March 31, 2019. Trained nurses collected their clinical information and blood samples.
Mol Biol Rep
January 2023
Department of Zoology, Lahore College for Women University, Lahore, Pakistan.
Background: CDK5 regulatory subunit associated protein 1 like 1 (CDKAL1) encodes a tRNA modifying enzyme involved in the proper protein translation and regulation of insulin production encoded by the CDKL gene. Sequence variations in the CDKAL1 gene lead to the misreading of the Lys codon in proinsulin, resulting in decreased glucose-stimulated proinsulin production. Various polymorphic sequence variants of the CDKAL1 gene such as rs7754840, rs7756992, rs9465871, and rs10946398 are reported to be associated with type 2 diabetes mellitus and gestational diabetes mellitus (GDM) incidence.
View Article and Find Full Text PDFJ Diabetes Res
March 2022
Health Management College, Anhui Medical University, Hefei, Anhui 230032, China.
Background: Diabetes is one of the common chronic diseases in which susceptibility is determined by a combination of genetic and environmental factors, and more than 90% of diabetic patients are diabetes mellitus type 2 (T2DM). The existing studies on the association between CDKAL1 rs10946398 gene polymorphism and susceptibility to type 2 diabetes are inconsistent across populations.
Aim: We aim to explore the association between CDKAL1 rs10946398 gene polymorphism and susceptibility to type 2 diabetes in different populations.
Diabetes Metab Syndr Obes
January 2021
Department of Endocrinology and Metabolism, The Second People's Hospital of Yunnan Province, & the Affiliated Hospital of Yunnan University, Kunming, Yunnan 650021, People's Republic of China.
Purpose: Type 2 diabetes mellitus (T2DM) has a high global prevalence, and the interaction of environmental factors and genetic factors may contribute to the risk of T2DM. We aimed to investigate the association between T2DM and the single nucleotide polymorphisms (SNPs) in genes ( and ) associated with insulin secretion.
Subjects And Methods: T2DM (n=1,169) and nondiabetic (NDM) (n=1,277) subjects were enrolled and the eight SNPs in and genes associated with insulin secretion were genotyped in a Chinese population using MassARRAY.
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