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Genetic overlap between autoimmune diseases and non-Hodgkin lymphoma subtypes.
Genetic Epidemiology ( IF 1.7 ) Pub Date : 2019-08-13 , DOI: 10.1002/gepi.22242
Lennox Din 1 , Mohammad Sheikh 1 , Nikitha Kosaraju 2 , Karin Ekstrom Smedby 3 , Sasha Bernatsky 4, 5 , Sonja I Berndt 6 , Christine F Skibola 7 , Alexandra Nieters 8 , Sophia Wang 9 , James D McKay 10 , Pierluigi Cocco 11 , Marc Maynadié 12 , Lenka Foretová 13 , Anthony Staines 14 , Thomas M Mack 15 , Silvia de Sanjosé 16, 17, 18 , Timothy J Vyse 19 , Leonid Padyukov 20 , Alain Monnereau 21, 22 , Alan A Arslan 23 , Amy Moore 6 , Angela R Brooks-Wilson 24, 25 , Anne J Novak 26 , Bengt Glimelius 27 , Brenda M Birmann 28 , Brian K Link 29 , Carolyn Stewart 30 , Claire M Vajdic 31 , Corinne Haioun 32 , Corrado Magnani 33 , David V Conti 34 , David G Cox 35 , Delphine Casabonne 17, 18 , Demetrius Albanes 6 , Eleanor Kane 36 , Eve Roman 36 , Giacomo Muzi 37 , Gilles Salles 38 , Graham G Giles 39, 40 , Hans-Olov Adami 41, 42 , Hervé Ghesquières 38 , Immaculata De Vivo 28, 43 , Jacqueline Clavel 44 , James R Cerhan 45 , John J Spinelli 46, 47 , Jonathan Hofmann 6 , Joseph Vijai 30 , Karen Curtin 48 , Karen H Costenbader 28 , Kenan Onel 49 , Kenneth Offit 50, 51 , Lauren R Teras 52 , Lindsay Morton 6 , Lucia Conde 53 , Lucia Miligi 54 , Mads Melbye 55, 56 , Maria Grazia Ennas 57 , Mark Liebow 26 , Mark P Purdue 58 , Martha Glenn 48 , Melissa C Southey 59, 60 , Morris Din 61 , Nathaniel Rothman 6 , Nicola J Camp 48, 62 , Nicole Wong Doo 63, 64 , Nikolaus Becker 65 , Nisha Pradhan 30 , Paige M Bracci 66 , Paolo Boffetta 67 , Paolo Vineis 68 , Paul Brennan 10 , Peter Kraft 69 , Qing Lan 6 , Richard K Severson 70 , Roel C H Vermeulen 71 , Roger L Milne 39, 40, 64 , Rudolph Kaaks 72 , Ruth C Travis 73 , Stephanie J Weinstein 6 , Stephen J Chanock 6 , Stephen M Ansell 26 , Susan L Slager 45 , Tongzhang Zheng 74 , Yawei Zhang 75 , Yolanda Benavente 17, 18 , Zachary Taub 76 , Lohith Madireddy 77 , Pierre-Antoine Gourraud 78, 79 , Jorge R Oksenberg 77 , Wendy Cozen 80 , Henrik Hjalgrim 55 , Pouya Khankhanian 2
Affiliation  

Epidemiologic studies show an increased risk of non-Hodgkin lymphoma (NHL) in patients with autoimmune disease (AD), due to a combination of shared environmental factors and/or genetic factors, or a causative cascade: chronic inflammation/antigen-stimulation in one disease leads to another. Here we assess shared genetic risk in genome-wide-association-studies (GWAS). Secondary analysis of GWAS of NHL subtypes (chronic lymphocytic leukemia, diffuse large B-cell lymphoma, follicular lymphoma, and marginal zone lymphoma) and ADs (rheumatoid arthritis, systemic lupus erythematosus, and multiple sclerosis). Shared genetic risk was assessed by (a) description of regional genetic of overlap, (b) polygenic risk score (PRS), (c)"diseasome", (d)meta-analysis. Descriptive analysis revealed few shared genetic factors between each AD and each NHL subtype. The PRS of ADs were not increased in NHL patients (nor vice versa). In the diseasome, NHLs shared more genetic etiology with ADs than solid cancers (p = .0041). A meta-analysis (combing AD with NHL) implicated genes of apoptosis and telomere length. This GWAS-based analysis four NHL subtypes and three ADs revealed few weakly-associated shared loci, explaining little total risk. This suggests common genetic variation, as assessed by GWAS in these sample sizes, may not be the primary explanation for the link between these ADs and NHLs.

中文翻译:


自身免疫性疾病和非霍奇金淋巴瘤亚型之间的遗传重叠。



流行病学研究表明,自身免疫性疾病 (AD) 患者患非霍奇金淋巴瘤 (NHL) 的风险增加,这是由于共同的环境因素和/或遗传因素的组合,或因果级联:慢性炎症/抗原刺激之一疾病导致另一种疾病。在这里,我们评估全基因组关联研究(GWAS)中的共同遗传风险。 NHL亚型(慢性淋巴细胞白血病、弥漫性大B细胞淋巴瘤、滤泡性淋巴瘤和边缘区淋巴瘤)和AD(类风湿性关节炎、系统性红斑狼疮和多发性硬化症)的GWAS二次分析。通过(a)重叠区域遗传的描述、(b)多基因风险评分(PRS)、(c)“疾病”、(d)荟萃分析来评估共有遗传风险。描述性分析显示每种 AD 和每种 NHL 亚型之间几乎没有共同的遗传因素。 NHL 患者的 AD 的 PRS 并未增加(反之亦然)。在疾病中,与实体癌相比,NHL 与 AD 具有更多的共同遗传病因 (p = .0041)。荟萃分析(将 AD 与 NHL 结合起来)表明细胞凋亡基因和端粒长度有关。这项基于 GWAS 的分析对四种 NHL 亚型和三种 AD 进行了分析,结果显示几乎没有弱相关的共享基因座,这几乎无法解释总风险。这表明通过 GWAS 在这些样本量中评估的常见遗传变异可能不是这些 AD 和 NHL 之间联系的主要解释。
更新日期:2019-11-01
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