Department of Endocrinology and Metabolism, Diskapi Yildirim Beyazit Teaching and Training Research Hospital, Ankara, Turkey.
Department of Medical Biology, Baskent University, Ankara, Turkey.
BMC Endocr Disord. 2019 May 20;19(1):51. doi: 10.1186/s12902-019-0375-2.
The molecular basis of the Turkish population with suspected maturity-onset diabetes of the young (MODY) has not been identified. This is the first study to investigate the association between HNF1A-gene single-nucleotide polymorphisms (SNPs) and having early-onset, MODY-like diabetes mellitus in the Turkish population.
All diabetic patients (N = 565) who presented to our clinic between 2012 and 2015 with a clinical suspicion of MODY were included in the study. Analysis of HNF1A, HNFB, HNF4A, GCK gene mutations was performed using real-time polymerase chain reaction sequencing. After genetic analysis, diabetics (n = 46) with HNF1A, HNF1B, HNF4A, GCK gene mutations (diagnosed as MODY) and diabetics (n = 30) with HNF1B, HNF4A, GCK gene SNPs were excluded. Patients with early-onset, MODY-like diabetes (n = 486) and non-diabetic controls (n = 263) were included. Genetic analyses for the HNF1A gene p.S487 N (rs2464196), p.A98V (rs1800574) and p.I27L (rs1169288) SNPs were performed using Sanger-based DNA sequencing among the control group.
p.S487 N and p.A98V was similar between the diabetics and controls in dominant and recessive models with no association (each, p > 0.05). p.I27L GT/TT carriers (GT/TT vs. GG, OR = 1.68, 95% CI: [1. 21-2.13]; p = 0.035) and p.I27L TT carriers had increased risk of having MODY-like diabetes (GT/GG vs. TT, OR = 1.56, 95% CI: [1. 14-2.57]; p = 0.048). Family inheritance of diabetes was significantly more common in patients with the p.I27L TT genotype. The p.I27L SNP was modestly associated with having diabetes after adjusting for body mass index and age (β = 1.45, 95% CI: [1. 2-4.2]; p = 0.036).
The HNF1A gene p.I27L SNP was modestly associated with having early-onset, MODY-like diabetes in the Turkish population. HNF1A gene p.I27L SNP might contribute to age at diabetes diagnosis and family inheritance.
疑似青年起病的成年型糖尿病(MODY)的土耳其人群的分子基础尚未确定。这是第一项研究,旨在调查 HNF1A 基因单核苷酸多态性(SNPs)与土耳其人群中早发、MODY 样糖尿病之间的关联。
所有在 2012 年至 2015 年间因疑似 MODY 而就诊于我院的糖尿病患者(N=565)均纳入本研究。采用实时聚合酶链反应测序分析 HNF1A、HNFB、HNF4A、GCK 基因突变。进行基因分析后,排除 HNF1A、HNF1B、HNF4A、GCK 基因突变(诊断为 MODY)的糖尿病患者(n=46)和 HNF1B、HNF4A、GCK 基因 SNPs 的糖尿病患者(n=30)。纳入早发、MODY 样糖尿病患者(n=486)和非糖尿病对照者(n=263)。在对照组中,采用 Sanger 测序法对 HNF1A 基因 p.S487N(rs2464196)、p.A98V(rs1800574)和 p.I27L(rs1169288)SNP 进行基因分析。
在显性和隐性模型中,糖尿病患者和对照组的 p.S487N 和 p.A98V 无差异(各 p>0.05)。p.I27L GT/TT 携带者(GT/TT 与 GG,OR=1.68,95%CI:[1.21-2.13];p=0.035)和 p.I27L TT 携带者发生 MODY 样糖尿病的风险增加(GT/GG 与 TT,OR=1.56,95%CI:[1.14-2.57];p=0.048)。p.I27L TT 基因型患者糖尿病家族遗传更为常见。调整体重指数和年龄后,p.I27L SNP 与糖尿病的发生有中度相关性(β=1.45,95%CI:[1.2-4.2];p=0.036)。
HNF1A 基因 p.I27L SNP 与土耳其人群中早发、MODY 样糖尿病有中度相关性。HNF1A 基因 p.I27L SNP 可能导致糖尿病的发病年龄和家族遗传。