Faleti Joseph O, Olasore Holiness S A, Olawale Matthew O, Murtala Abdullahi A, Banjo Taiwo O, Igwo-Ezikpe Miriam N
Department of Biochemistry, College of Medicine, University of Lagos, Idi-Araba Campus, Surulere, Lagos State, Nigeria.
Department of Pharmacology and Therapeutics, Obafemi Awolowo College of Health Sciences, Olabisi Onabanjo University, Sagamu Campus, Sagamu, Ogun State, Nigeria.
Biochem Genet. 2025 Feb 3. doi: 10.1007/s10528-025-11039-w.
Genetic variations in the lipoprotein lipase (LPL) gene including the HindIII polymorphism (rs320) have been reported to modify fat metabolism, adiposity, and body weight. However, little attention has been given to the African population. The present study aimed to investigate the relationship between the rs320 gene polymorphism and a number of metabolic and anthropometric parameters in a sample of the Nigerian population. We recruited 236 participants for the study. The participants were required to sign informed consent forms after which information related to their calorie intake and utilization as well as anthropometric measurements were recorded. Plasma metabolic parameters were subsequently determined using an autoanalyzer. Genotyping for HindIII polymorphism was performed using the PCR-RFLP method. The frequencies (n) of T and G alleles were 0.841 (397) and 0.158 (75), while the frequencies (n) of TT, TG, and GG were 0.691(163), 0.301(71), and 0.01(2), respectively. The population was not in Hardy-Weinberg equilibrium (χ = 3.717, df = 1, p = 0.841). The anthropometric parameters, the fasting blood glucose, and low-density lipoprotein cholesterol showed no association with the alleles, while plasma high-density lipoprotein cholesterol and total cholesterol were significantly higher among the G allele carriers. However, triglyceride and total protein were significantly higher among the non-G allele carriers. The LPL HindIII gene polymorphism is associated with changes in plasma lipid profile in a sample of the Nigerian population.
据报道,脂蛋白脂肪酶(LPL)基因的遗传变异,包括HindIII多态性(rs320),会改变脂肪代谢、肥胖程度和体重。然而,非洲人群却很少受到关注。本研究旨在调查尼日利亚人群样本中rs320基因多态性与一些代谢和人体测量参数之间的关系。我们招募了236名参与者进行研究。参与者需要签署知情同意书,之后记录与他们的卡路里摄入和利用以及人体测量相关的信息。随后使用自动分析仪测定血浆代谢参数。采用PCR-RFLP方法对HindIII多态性进行基因分型。T和G等位基因的频率(n)分别为0.841(397)和0.158(75),而TT、TG和GG的频率(n)分别为0.691(163)、0.301(71)和0.01(2)。该人群不符合哈迪-温伯格平衡(χ = 3.717,自由度 = 1,p = 0.841)。人体测量参数、空腹血糖和低密度脂蛋白胆固醇与等位基因无关联,而G等位基因携带者中的血浆高密度脂蛋白胆固醇和总胆固醇显著更高。然而,非G等位基因携带者中的甘油三酯和总蛋白显著更高。LPL HindIII基因多态性与尼日利亚人群样本中的血浆脂质谱变化有关。