3-羟基-3-甲基戊二酰辅酶 A 还原酶基因的常见和罕见遗传变异与白内障风险的关系

Jonas Ghouse, Gustav Ahlberg, Anne Guldhammer Skov, Henning Bundgaard, Morten S Olesen
{"title":"3-羟基-3-甲基戊二酰辅酶 A 还原酶基因的常见和罕见遗传变异与白内障风险的关系","authors":"Jonas Ghouse, Gustav Ahlberg, Anne Guldhammer Skov, Henning Bundgaard, Morten S Olesen","doi":"10.1161/JAHA.122.025361","DOIUrl":null,"url":null,"abstract":"<p><p>Background Results from animal models and observational studies have raised concerns regarding the potential cataractogenic effects of statin treatment. We investigated whether common and rare genetic variants in <i>HMGCR</i> are associated with cataract risk, to gauge the likely long-term effects of statin treatment on lenticular opacities. Methods and Results We used genotyping data and exome sequencing data of unrelated European individuals in the UK Biobank to test the association between genetically proxied inhibition of <i>HMGCR</i> and cataract risk. First, we constructed an <i>HMGCR</i> genetic score consisting of 5 common variants weighted by their association with low-density lipoprotein cholesterol. Second, we analyzed exome sequencing data to identify carriers of predicted loss-of-function mutations in <i>HMGCR</i>. Common and rare variants in aggregate were then tested for association with cataract and cataract surgery. In an analysis of >402 000 individuals, a 38.7 mg/dL (1 mmol/L) reduction in low-density lipoprotein C by the <i>HMGCR</i> genetic score was associated with higher risk for cataract (odds ratio, 1.14 [95% CI, 1.00-1.39], <i>P</i>=0.045) and cataract surgery (odds ratio, 1.25 [95% CI, 1.06-1.48], <i>P</i>=0.009). Among 169 172 individuals with <i>HMGCR</i> sequencing data, we identified 32 participants (0.02%), who carried a rare <i>HMGCR</i> predicted loss-of-function variant. Compared with noncarriers, heterozygous carriers of <i>HMGCR</i> predicted loss-of-function had a higher risk of developing cataract (odds ratio, 4.54 [95% CI, 1.96-10.53], <i>P</i>=0.001) and cataract surgery (odds ratio, 5.27 [95% CI, 2.27-12.25]<i>, P</i>=5.37×10<sup>-4</sup>). In exploratory analyses, we found no significant association between genetically proxied inhibition of <i>PCSK9, NPC1L1</i>, or circulating low-density lipoprotein cholesterol levels (<i>P</i>>0.05 for all) and cataract risk. Conclusions We found that genetically proxied inhibition of the <i>HMGCR</i> gene mimicking long-term statin treatment associated with higher risk of cataract. Clinical trials with longer follow-up are needed to confirm these findings.</p>","PeriodicalId":17189,"journal":{"name":"Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2022-06-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9238641/pdf/","citationCount":"0","resultStr":"{\"title\":\"Association of Common and Rare Genetic Variation in the 3-Hydroxy-3-Methylglutaryl Coenzyme A Reductase Gene and Cataract Risk.\",\"authors\":\"Jonas Ghouse, Gustav Ahlberg, Anne Guldhammer Skov, Henning Bundgaard, Morten S Olesen\",\"doi\":\"10.1161/JAHA.122.025361\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Background Results from animal models and observational studies have raised concerns regarding the potential cataractogenic effects of statin treatment. We investigated whether common and rare genetic variants in <i>HMGCR</i> are associated with cataract risk, to gauge the likely long-term effects of statin treatment on lenticular opacities. Methods and Results We used genotyping data and exome sequencing data of unrelated European individuals in the UK Biobank to test the association between genetically proxied inhibition of <i>HMGCR</i> and cataract risk. First, we constructed an <i>HMGCR</i> genetic score consisting of 5 common variants weighted by their association with low-density lipoprotein cholesterol. Second, we analyzed exome sequencing data to identify carriers of predicted loss-of-function mutations in <i>HMGCR</i>. Common and rare variants in aggregate were then tested for association with cataract and cataract surgery. In an analysis of >402 000 individuals, a 38.7 mg/dL (1 mmol/L) reduction in low-density lipoprotein C by the <i>HMGCR</i> genetic score was associated with higher risk for cataract (odds ratio, 1.14 [95% CI, 1.00-1.39], <i>P</i>=0.045) and cataract surgery (odds ratio, 1.25 [95% CI, 1.06-1.48], <i>P</i>=0.009). Among 169 172 individuals with <i>HMGCR</i> sequencing data, we identified 32 participants (0.02%), who carried a rare <i>HMGCR</i> predicted loss-of-function variant. Compared with noncarriers, heterozygous carriers of <i>HMGCR</i> predicted loss-of-function had a higher risk of developing cataract (odds ratio, 4.54 [95% CI, 1.96-10.53], <i>P</i>=0.001) and cataract surgery (odds ratio, 5.27 [95% CI, 2.27-12.25]<i>, P</i>=5.37×10<sup>-4</sup>). In exploratory analyses, we found no significant association between genetically proxied inhibition of <i>PCSK9, NPC1L1</i>, or circulating low-density lipoprotein cholesterol levels (<i>P</i>>0.05 for all) and cataract risk. Conclusions We found that genetically proxied inhibition of the <i>HMGCR</i> gene mimicking long-term statin treatment associated with higher risk of cataract. Clinical trials with longer follow-up are needed to confirm these findings.</p>\",\"PeriodicalId\":17189,\"journal\":{\"name\":\"Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2022-06-21\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9238641/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1161/JAHA.122.025361\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2022/6/15 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1161/JAHA.122.025361","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2022/6/15 0:00:00","PubModel":"Epub","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

背景 动物模型和观察性研究的结果引起了人们对他汀类药物治疗可能导致白内障的担忧。我们调查了 HMGCR 中常见和罕见的基因变异是否与白内障风险相关,以评估他汀类药物治疗对光栅不透明可能产生的长期影响。方法和结果 我们利用英国生物库中无关欧洲人的基因分型数据和外显子组测序数据,检验了HMGCR基因替代抑制与白内障风险之间的关联。首先,我们构建了一个 HMGCR 遗传评分,该评分由 5 个常见变体组成,并根据其与低密度脂蛋白胆固醇的关系进行加权。其次,我们分析了外显子组测序数据,以确定预测的 HMGCR 功能缺失突变的携带者。然后,我们检测了常见和罕见变异与白内障和白内障手术的关系。在对超过 402 000 人的分析中,根据 HMGCR 基因评分,低密度脂蛋白 C 减少 38.7 毫克/分升(1 毫摩尔/升)与白内障(几率比为 1.14 [95% CI, 1.00-1.39],P=0.045)和白内障手术(几率比为 1.25 [95% CI, 1.06-1.48],P=0.009)风险较高有关。在 169 172 名有 HMGCR 测序数据的个体中,我们发现 32 名参与者(0.02%)携带罕见的 HMGCR 预测功能缺失变异。与非携带者相比,HMGCR 预测功能缺失杂合子携带者患白内障(几率比为 4.54 [95% CI, 1.96-10.53],P=0.001)和白内障手术(几率比为 5.27 [95% CI, 2.27-12.25],P=5.37×10-4)的风险更高。在探索性分析中,我们发现 PCSK9、NPC1L1 或循环中的低密度脂蛋白胆固醇水平的基因代理抑制与白内障风险之间没有明显的关联(P>0.05)。结论 我们发现,模拟长期他汀类药物治疗的 HMGCR 基因基因替代抑制与较高的白内障风险有关。要证实这些发现,还需要进行更长时间的临床试验。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Association of Common and Rare Genetic Variation in the 3-Hydroxy-3-Methylglutaryl Coenzyme A Reductase Gene and Cataract Risk.

Background Results from animal models and observational studies have raised concerns regarding the potential cataractogenic effects of statin treatment. We investigated whether common and rare genetic variants in HMGCR are associated with cataract risk, to gauge the likely long-term effects of statin treatment on lenticular opacities. Methods and Results We used genotyping data and exome sequencing data of unrelated European individuals in the UK Biobank to test the association between genetically proxied inhibition of HMGCR and cataract risk. First, we constructed an HMGCR genetic score consisting of 5 common variants weighted by their association with low-density lipoprotein cholesterol. Second, we analyzed exome sequencing data to identify carriers of predicted loss-of-function mutations in HMGCR. Common and rare variants in aggregate were then tested for association with cataract and cataract surgery. In an analysis of >402 000 individuals, a 38.7 mg/dL (1 mmol/L) reduction in low-density lipoprotein C by the HMGCR genetic score was associated with higher risk for cataract (odds ratio, 1.14 [95% CI, 1.00-1.39], P=0.045) and cataract surgery (odds ratio, 1.25 [95% CI, 1.06-1.48], P=0.009). Among 169 172 individuals with HMGCR sequencing data, we identified 32 participants (0.02%), who carried a rare HMGCR predicted loss-of-function variant. Compared with noncarriers, heterozygous carriers of HMGCR predicted loss-of-function had a higher risk of developing cataract (odds ratio, 4.54 [95% CI, 1.96-10.53], P=0.001) and cataract surgery (odds ratio, 5.27 [95% CI, 2.27-12.25], P=5.37×10-4). In exploratory analyses, we found no significant association between genetically proxied inhibition of PCSK9, NPC1L1, or circulating low-density lipoprotein cholesterol levels (P>0.05 for all) and cataract risk. Conclusions We found that genetically proxied inhibition of the HMGCR gene mimicking long-term statin treatment associated with higher risk of cataract. Clinical trials with longer follow-up are needed to confirm these findings.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信