Nejati Majid, Atlasi Mohammad Ali, Karimian Mohammad, Nikzad Hossein, Azami Tameh Abolfazl
Anatomical Sciences Research Center, Kashan University of Medical Sciences, Kashan, Iran.
Iran J Basic Med Sci. 2018 Jul;21(7):701-708. doi: 10.22038/IJBMS.2018.29009.7001.
Stroke is the most common neurological disorder and genetic susceptibility has an important role in its etiology. Polymorphism in several genes such as lipoprotein lipase () is propounded as a risk for stroke. This meta-analysis investigated the association of rs285 and rs320 LPL polymorphism with stroke risk.
We searched PubMed, Clarivate Analytics Web of Science, Google Scholar, and Science Direct databases for appropriate studies. The odds ratios (ORs) with 95% confidence intervals (CIs) were calculated to estimate the strength of this association. Also, the effects of four common polymorphisms (rs268, rs285, rs320, and rs328) on the molecular aspects of LPL were evaluated by tools. Five studies were included in meta-analysis after screening.
Our data indicated that rs320 significantly decreased the risk of stroke (G vs. T: OR= 0.64, 95%CI=0.54-0.76; GG vs. TT: OR=0.47, 95%CI=0.29-0.75; TG vs. TT: OR=0.65, 95%CI=0.53-0.80; TG+GG vs. TT: OR=0.62, 95%CI=0.51-0.75; GG vs. TT+TG: OR=0.51, 95%CI=0.32-0.82). Moreover, a significant association between rs285 and diminution of stroke risk was seen (P- vs. P+: OR=0.72, 95%CI=0.58-0.91; P-P- vs. P+P+: OR=0.50, 95%CI=0.31-0.82; P+P-+P-P- vs. P+P+: OR=0.72, 95%CI=0.53-0.96; P-P- vs. P+P++P+P-: OR=0.581, 95%CI=0.369-0.916). Also, the same results were observed after stratifying, without any publication bias (>0.05). Furthermore, computational analysis revealed that rs268 and rs328 may affect the protein structure (prediction: non-neutral; score=19; expected accuracy=59%) while rs320 could affect the RNA structure (distance=0.2264, -value=0.0534; <0.2 is significant).
This meta-analysis indicated that risk of stroke was decreased in rs320 and rs285 polymorphisms in the LPL gene.
中风是最常见的神经系统疾病,遗传易感性在其病因中起重要作用。若干基因如脂蛋白脂肪酶(LPL)的多态性被认为是中风的危险因素。本荟萃分析研究了rs285和rs320 LPL多态性与中风风险的关联。
我们在PubMed、科睿唯安Web of Science、谷歌学术和Science Direct数据库中搜索相关研究。计算比值比(OR)及95%置信区间(CI)以评估这种关联的强度。此外,还通过工具评估了四种常见多态性(rs268、rs285、rs320和rs328)对LPL分子层面的影响。筛选后纳入五项研究进行荟萃分析。
我们的数据表明,rs320显著降低中风风险(G vs. T:OR = 0.64,95%CI = 0.54 - 0.76;GG vs. TT:OR = 0.47,95%CI = 0.29 - 0.75;TG vs. TT:OR = 0.65,95%CI = 0.53 - 0.80;TG + GG vs. TT:OR = 0.62,95%CI = 0.51 - 0.75;GG vs. TT + TG:OR = 0.51,95%CI = 0.32 - 0.82)。此外,rs285与中风风险降低之间存在显著关联(P - vs. P +:OR = 0.72,95%CI = 0.58 - 0.91;P - P - vs. P + P +:OR = 0.50,95%CI = 0.31 - 0.82;P + P - + P - P - vs. P + P +:OR = 0.72,95%CI = 0.53 - 0.96;P - P - vs. P + P + + P + P -:OR = 0.581,95%CI = 0.369 - 0.916)。分层分析后也得到相同结果,且无任何发表偏倚(P > 0.05)。此外,计算分析表明rs268和rs328可能影响蛋白质结构(预测:非中性;得分 = 19;预期准确率 = 59%),而rs320可能影响RNA结构(距离 = 0.2264,P值 = 0.0534;P < 0.2具有显著性)。
本荟萃分析表明,LPL基因中的rs320和rs285多态性可降低中风风险。