父母血缘和家族史与银屑病的关系及性别的作用:一项病例对照研究。

IF 1.1 4区 生物学 Q4 GENETICS & HEREDITY Human Heredity Pub Date : 2025-01-01 Epub Date: 2024-12-31 DOI:10.1159/000543351
Alanood N AlKhas, Ali H Ziyab
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引用次数: 0

摘要

简介:银屑病是由内在因素和外在因素相互作用引起的。亲本血缘关系增加了后代基因组的纯合性,这反过来又增加了患病风险。亲代血缘关系与后代牛皮癣之间的关系仍未得到研究。因此,本研究试图评估父母血缘和家族史与后代牛皮癣的关系,并确定性别是否调节上述关系。方法:一项病例对照研究纳入了21岁及以上的成年人。由皮肤科医生诊断的牛皮癣病例(n=139)来自皮肤科诊所。对照组(无牛皮癣受试者;N =278)从工作场所招募。研究对象报告了父母亲属关系和牛皮癣家族史的信息。应用逻辑回归评估相关性,并估计校正优势比(aOR)和95%置信区间(CI)。结果:与对照组相比,病例更有可能报告父母血缘关系(59.7% vs 35.6%;结论:与对照组相比,银屑病患者报告父母亲属关系和银屑病家族史的可能性明显更高,父母亲属关系仅与男性银屑病有关。
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Parental Consanguinity and Family History in Relation to Psoriasis and the Role of Sex: A Case-Control Study.

Introduction: Psoriasis is caused by an interplay between intrinsic and extrinsic factors. Parental consanguinity increases homozygosity in the genome of the offspring, which in turn increases disease risk. The association between parental consanguinity and psoriasis in the offspring remains unexplored. Therefore, this study sought to evaluate the association of parental consanguinity and family history with psoriasis in the offspring and to determine whether sex modulates the aforementioned associations.

Methods: A case-control study enrolled adults aged 21 years and more. Psoriasis cases (n = 139) diagnosed by dermatologists were enrolled from dermatology clinics. Controls (psoriasis-free subjects; n = 278) were enrolled from workplaces. Study subjects reported information on parental consanguinity and family history of psoriasis. Logistic regression was applied to evaluate associations, and adjusted odds ratios (aOR) and 95% confidence intervals (CIs) were estimated.

Results: Cases compared to controls were more likely to report parental consanguinity (59.7% vs. 35.6%; p < 0.001) and family history of psoriasis (56.8% vs. 23.7%; p < 0.001). Both parental consanguinity (aOR: 2.13, 95% CI: 1.29-3.50) and family history of psoriasis (aOR: 3.43, 95% CI: 2.07-5.67) were associated with increased odds of having psoriasis. The observed association between parental consanguinity and psoriasis differed according to sex (pinteraction = 0.008), with parental consanguinity being associated with psoriasis among males (aOR: 5.96, 95% CI: 2.39-14.82), but not among females (aOR: 1.36, 95% CI: 0.75-2.49).

Conclusion: Psoriasis cases compared to controls were significantly more likely to report parental consanguinity and family history of psoriasis, with parental consanguinity being associated with psoriasis among males only.

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来源期刊
Human Heredity
Human Heredity 生物-遗传学
CiteScore
2.50
自引率
0.00%
发文量
12
审稿时长
>12 weeks
期刊介绍: Gathering original research reports and short communications from all over the world, ''Human Heredity'' is devoted to methodological and applied research on the genetics of human populations, association and linkage analysis, genetic mechanisms of disease, and new methods for statistical genetics, for example, analysis of rare variants and results from next generation sequencing. The value of this information to many branches of medicine is shown by the number of citations the journal receives in fields ranging from immunology and hematology to epidemiology and public health planning, and the fact that at least 50% of all ''Human Heredity'' papers are still cited more than 8 years after publication (according to ISI Journal Citation Reports). Special issues on methodological topics (such as ‘Consanguinity and Genomics’ in 2014; ‘Analyzing Rare Variants in Complex Diseases’ in 2012) or reviews of advances in particular fields (‘Genetic Diversity in European Populations: Evolutionary Evidence and Medical Implications’ in 2014; ‘Genes and the Environment in Obesity’ in 2013) are published every year. Renowned experts in the field are invited to contribute to these special issues.
期刊最新文献
Parental Consanguinity and Family History in Relation to Psoriasis and the Role of Sex: A Case-Control Study. Place of concordance-discordance model in evaluating NGS performance. Implications of the Co-Dominance Model for Hardy-Weinberg Testing in Genetic Association Studies. Joint Linkage and Association Analysis Using GENEHUNTER-MODSCORE with an Application to Familial Pancreatic Cancer. Investigation of Recessive Effects of Coding Variants on Common Clinical Phenotypes in Exome-Sequenced UK Biobank Participants.
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