• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

相似文献

1
A common genetic variant in the 15q24 nicotinic acetylcholine receptor gene cluster (CHRNA5-CHRNA3-CHRNB4) is associated with a reduced ability of women to quit smoking in pregnancy.15号染色体长臂24区烟碱型乙酰胆碱受体基因簇(CHRNA5-CHRNA3-CHRNB4)中的一种常见基因变异与女性孕期戒烟能力下降有关。
Hum Mol Genet. 2009 Aug 1;18(15):2922-7. doi: 10.1093/hmg/ddp216. Epub 2009 May 9.
2
Association Between rs1051730 and Smoking During Pregnancy in Dutch Women.荷兰女性 rs1051730 与孕期吸烟的关联性研究。
Nicotine Tob Res. 2019 May 21;21(6):835-840. doi: 10.1093/ntr/ntx267.
3
Beyond cigarettes per day. A genome-wide association study of the biomarker carbon monoxide.不仅仅是每天吸多少支烟。生物标志物一氧化碳的全基因组关联研究。
Ann Am Thorac Soc. 2014 Sep;11(7):1003-10. doi: 10.1513/AnnalsATS.201401-010OC.
4
Genetic variation in the 15q25 nicotinic acetylcholine receptor gene cluster (CHRNA5-CHRNA3-CHRNB4) interacts with maternal self-reported smoking status during pregnancy to influence birth weight.15q25 尼古丁型乙酰胆碱受体基因簇(CHRNA5-CHRNA3-CHRNB4)的遗传变异与母亲在怀孕期间自我报告的吸烟状况相互作用,影响出生体重。
Hum Mol Genet. 2012 Dec 15;21(24):5344-58. doi: 10.1093/hmg/dds372. Epub 2012 Sep 5.
5
Markers in the 15q24 nicotinic receptor subunit gene cluster (CHRNA5-A3-B4) predict severity of nicotine addiction and response to smoking cessation therapy.15q24 尼古丁受体亚基基因簇(CHRNA5-A3-B4)中的标志物可预测尼古丁成瘾的严重程度和对戒烟治疗的反应。
Am J Med Genet B Neuropsychiatr Genet. 2011 Apr;156B(3):275-84. doi: 10.1002/ajmg.b.31155. Epub 2011 Jan 25.
6
Variant within the promoter region of the CHRNA3 gene associated with FTN dependence is not related to self-reported willingness to quit smoking.与依赖氟烷相关的 CHRNA3 基因启动子区域内的变异与自我报告的戒烟意愿无关。
Nicotine Tob Res. 2011 Sep;13(9):833-9. doi: 10.1093/ntr/ntr084. Epub 2011 Apr 21.
7
Association of serum cotinine level with a cluster of three nicotinic acetylcholine receptor genes (CHRNA3/CHRNA5/CHRNB4) on chromosome 15.血清可替宁水平与染色体 15 上三个烟碱型乙酰胆碱受体基因(CHRNA3/CHRNA5/CHRNB4)簇的关联。
Hum Mol Genet. 2009 Oct 15;18(20):4007-12. doi: 10.1093/hmg/ddp322. Epub 2009 Jul 23.
8
Analysis of detailed phenotype profiles reveals CHRNA5-CHRNA3-CHRNB4 gene cluster association with several nicotine dependence traits.分析详细的表型谱揭示 CHRNA5-CHRNA3-CHRNB4 基因簇与多种尼古丁依赖特征相关。
Nicotine Tob Res. 2012 Jun;14(6):720-33. doi: 10.1093/ntr/ntr283. Epub 2012 Jan 12.
9
Risk gene variants for nicotine dependence in the CHRNA5-CHRNA3-CHRNB4 cluster are associated with cognitive performance.与尼古丁依赖相关的 CHRNA5-CHRNA3-CHRNB4 簇中的风险基因变异与认知表现相关。
Am J Med Genet B Neuropsychiatr Genet. 2010 Dec 5;153B(8):1448-58. doi: 10.1002/ajmg.b.31126. Epub 2010 Sep 30.
10
The CHRNA5-CHRNA3-CHRNB4 nicotinic receptor subunit gene cluster affects risk for nicotine dependence in African-Americans and in European-Americans.CHRNA5-CHRNA3-CHRNB4烟碱受体亚基基因簇影响非裔美国人和欧裔美国人对尼古丁依赖的风险。
Cancer Res. 2009 Sep 1;69(17):6848-56. doi: 10.1158/0008-5472.CAN-09-0786. Epub 2009 Aug 25.

引用本文的文献

1
Relationship between tobacco smoking and metabolic syndrome: a Mendelian randomization analysis.吸烟与代谢综合征之间的关系:孟德尔随机化分析
BMC Endocr Disord. 2025 Mar 28;25(1):87. doi: 10.1186/s12902-025-01910-7.
2
Exploring and Accounting for Genetically Driven Effect Heterogeneity in Mendelian Randomization.探索并解释孟德尔随机化中基因驱动的效应异质性
Genet Epidemiol. 2025 Jan;49(1):e22587. doi: 10.1002/gepi.22587. Epub 2024 Sep 22.
3
A multi-ancestry cerebral cortex transcriptome-wide association study identifies genes associated with smoking behaviors.一项多血统大脑皮层转录组全基因组关联研究鉴定出与吸烟行为相关的基因。
Mol Psychiatry. 2024 Nov;29(11):3580-3589. doi: 10.1038/s41380-024-02605-6. Epub 2024 May 30.
4
Smoking during pregnancy and its effect on placental weight: a Mendelian randomization study.孕期吸烟及其对胎盘重量的影响:一项孟德尔随机化研究。
BMC Pregnancy Childbirth. 2024 Apr 4;24(1):238. doi: 10.1186/s12884-024-06431-0.
5
Genetic Associations with Smoking Relapse and Proportion of Follow-up in Smoking Relapse throughout Adulthood in Pre- and Postmenopausal Women.绝经前和绝经后女性整个成年期吸烟复发与遗传相关性及吸烟复发随访比例。
Cancer Prev Res (Phila). 2023 May 1;16(5):269-279. doi: 10.1158/1940-6207.CAPR-22-0421.
6
CHRNA5-A3-B4 and DRD2 Genes and Smoking Cessation Throughout Adulthood: A Longitudinal Study of Women.CHRNA5-A3-B4 和 DRD2 基因与成年期戒烟:一项女性的纵向研究。
Nicotine Tob Res. 2023 May 22;25(6):1164-1173. doi: 10.1093/ntr/ntad026.
7
Using genomic profiling for understanding and improving response to smoking cessation treatment.利用基因组分析来理解和改善对戒烟治疗的反应。
Curr Epidemiol Rep. 2019 Dec;6(4):486-490. doi: 10.1007/s40471-019-00220-6. Epub 2019 Oct 17.
8
A systematic review of genetic variation within nicotinic acetylcholine receptor genes and cigarette smoking cessation.尼古丁型乙酰胆碱受体基因内遗传变异与戒烟的系统评价。
Drug Alcohol Depend. 2022 Oct 1;239:109596. doi: 10.1016/j.drugalcdep.2022.109596. Epub 2022 Aug 5.
9
rs16969968 and rs578776 polymorphisms are associated with multiple nicotine dependence phenotypes in Bangladeshi smokers.rs16969968和rs578776基因多态性与孟加拉吸烟者的多种尼古丁依赖表型相关。
Heliyon. 2022 Jul 14;8(7):e09947. doi: 10.1016/j.heliyon.2022.e09947. eCollection 2022 Jul.
10
The potential of DNA methylation as a biomarker for obesity and smoking.DNA 甲基化作为肥胖和吸烟生物标志物的潜力。
J Intern Med. 2022 Sep;292(3):390-408. doi: 10.1111/joim.13496. Epub 2022 Apr 19.

本文引用的文献

1
Six new loci associated with body mass index highlight a neuronal influence on body weight regulation.六个与体重指数相关的新基因座凸显了神经元对体重调节的影响。
Nat Genet. 2009 Jan;41(1):25-34. doi: 10.1038/ng.287. Epub 2008 Dec 14.
2
Nicotinic acetylcholine receptor beta2 subunit gene implicated in a systems-based candidate gene study of smoking cessation.烟碱型乙酰胆碱受体β2亚基基因与一项基于系统的戒烟候选基因研究有关。
Hum Mol Genet. 2008 Sep 15;17(18):2834-48. doi: 10.1093/hmg/ddn181. Epub 2008 Jul 1.
3
Variants in nicotinic receptors and risk for nicotine dependence.烟碱型受体变体与尼古丁依赖风险
Am J Psychiatry. 2008 Sep;165(9):1163-71. doi: 10.1176/appi.ajp.2008.07111711. Epub 2008 Jun 2.
4
Common variants near MC4R are associated with fat mass, weight and risk of obesity.MC4R基因附近的常见变异与脂肪量、体重及肥胖风险相关。
Nat Genet. 2008 Jun;40(6):768-75. doi: 10.1038/ng.140. Epub 2008 May 4.
5
Genetic influences on smoking cessation and relapse in pregnant women.基因对孕妇戒烟及复吸的影响。
J Obstet Gynaecol. 2008 Feb;28(2):155-60. doi: 10.1080/01443610801912725.
6
A variant associated with nicotine dependence, lung cancer and peripheral arterial disease.一种与尼古丁依赖、肺癌和外周动脉疾病相关的变体。
Nature. 2008 Apr 3;452(7187):638-642. doi: 10.1038/nature06846.
7
A susceptibility locus for lung cancer maps to nicotinic acetylcholine receptor subunit genes on 15q25.肺癌的一个易感基因座定位于15号染色体长臂25区的烟碱型乙酰胆碱受体亚基基因。
Nature. 2008 Apr 3;452(7187):633-7. doi: 10.1038/nature06885.
8
Genome-wide association scan of tag SNPs identifies a susceptibility locus for lung cancer at 15q25.1.标签单核苷酸多态性的全基因组关联扫描在15q25.1处鉴定出一个肺癌易感位点。
Nat Genet. 2008 May;40(5):616-22. doi: 10.1038/ng.109. Epub 2008 Apr 2.
9
Common variation in the FTO gene alters diabetes-related metabolic traits to the extent expected given its effect on BMI.FTO基因的常见变异对与糖尿病相关的代谢特征产生的影响,与基于其对体重指数的作用所预期的程度相符。
Diabetes. 2008 May;57(5):1419-26. doi: 10.2337/db07-1466. Epub 2008 Mar 17.
10
Alpha-5/alpha-3 nicotinic receptor subunit alleles increase risk for heavy smoking.α-5/α-3烟碱受体亚基等位基因会增加重度吸烟的风险。
Mol Psychiatry. 2008 Apr;13(4):368-73. doi: 10.1038/sj.mp.4002154. Epub 2008 Jan 29.

15号染色体长臂24区烟碱型乙酰胆碱受体基因簇(CHRNA5-CHRNA3-CHRNB4)中的一种常见基因变异与女性孕期戒烟能力下降有关。

A common genetic variant in the 15q24 nicotinic acetylcholine receptor gene cluster (CHRNA5-CHRNA3-CHRNB4) is associated with a reduced ability of women to quit smoking in pregnancy.

作者信息

Freathy Rachel M, Ring Susan M, Shields Beverley, Galobardes Bruna, Knight Beatrice, Weedon Michael N, Smith George Davey, Frayling Timothy M, Hattersley Andrew T

机构信息

Genetics of Complex Traits, Peninsula Medical School, Institute of Biomedical and Clinical Science, Magdalen Road, Exeter EX1 2LU, UK.

出版信息

Hum Mol Genet. 2009 Aug 1;18(15):2922-7. doi: 10.1093/hmg/ddp216. Epub 2009 May 9.

DOI:10.1093/hmg/ddp216
PMID:19429911
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2706684/
Abstract

Maternal smoking during pregnancy is associated with low birth weight and adverse pregnancy outcomes. Women are more likely to quit smoking during pregnancy than at any other time in their lives, but some pregnant women continue to smoke. A recent genome-wide association study demonstrated an association between a common polymorphism (rs1051730) in the nicotinic acetylcholine receptor gene cluster (CHRNA5-CHRNA3-CHRNB4) and both smoking quantity and nicotine dependence. We aimed to test whether the same polymorphism that predisposes to greater cigarette consumption would also reduce the likelihood of smoking cessation in pregnancy. We studied 7845 pregnant women of European descent from the South-West of England. Using 2474 women who smoked regularly immediately pre-pregnancy, we analysed the association between the rs1051730 risk allele and both smoking cessation during pregnancy and smoking quantity. Each additional copy of the risk allele was associated with a 1.27-fold higher odds (95% CI 1.11-1.45) of continued smoking during pregnancy (P = 0.0006). Adjustment for pre-pregnancy smoking quantity weakened, but did not remove this association [odds ratio (OR) 1.20 (95% CI 1.03-1.39); P = 0.018]. The same risk allele was also associated with heavier smoking before pregnancy and in the first, but not the last, trimester [OR for smoking 10+ cigarettes/day versus 1-9/day in first trimester = 1.30 (95% CI 1.13-1.50); P = 0.0003]. To conclude, we have found strong evidence of association between the rs1051730 variant and an increased likelihood of continued smoking in pregnancy and have confirmed the previously observed association with smoking quantity. Our data support the role of genetic factors in influencing smoking cessation during pregnancy.

摘要

孕期母亲吸烟与低出生体重及不良妊娠结局相关。女性在孕期比一生中的其他任何时候都更有可能戒烟,但仍有一些孕妇继续吸烟。最近一项全基因组关联研究表明,烟碱型乙酰胆碱受体基因簇(CHRNA5-CHRNA3-CHRNB4)中的一种常见多态性(rs1051730)与吸烟量及尼古丁依赖均有关联。我们旨在测试,这种导致更多香烟消费量的相同多态性是否也会降低孕期戒烟的可能性。我们研究了来自英格兰西南部的7845名欧洲裔孕妇。以2474名孕前经常吸烟的女性为研究对象,我们分析了rs1051730风险等位基因与孕期戒烟及吸烟量之间的关联。风险等位基因每增加一份拷贝,与孕期继续吸烟的几率高出1.27倍(95%置信区间1.11-1.45)相关(P = 0.0006)。对孕前吸烟量进行校正后,这种关联虽有所减弱,但并未消除[比值比(OR)1.20(95%置信区间1.03-1.39);P = 0.018]。相同的风险等位基因还与孕前及孕早期(而非孕晚期)吸烟量更大有关[孕早期每天吸烟10支及以上与每天吸烟1-9支相比的OR = 1.30(95%置信区间1.13-1.50);P = 0.0003]。总之,我们发现了有力证据,表明rs1051730变异与孕期继续吸烟可能性增加之间存在关联,并证实了之前观察到的与吸烟量的关联。我们的数据支持遗传因素在影响孕期戒烟方面的作用。