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种族同质家系中手部骨关节炎的遗传模式。

Mode of inheritance of hand osteoarthritis in ethnically homogeneous pedigrees.

作者信息

Livshits Gregory, Kalichman Leonid, Cohen Zvl, Kobyliansky Eugene

机构信息

Research Unit, Human Population Biology, Department of Anatomy and Anthropology, Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.

出版信息

Hum Biol. 2002 Dec;74(6):849-60. doi: 10.1353/hub.2003.0009.

Abstract

The aim of the present study was to investigate the extent and mode of inheritance of hand osteoarthritis (OA) using a large sample of ethnically homogeneous pedigrees. Two types of segregation analysis (SA) models were examined. Type I models used the data adjusted for potential significant covariates, particularly age and sex, prior to genetic analysis. Type 11 models incorporated effects of the potential covariates into major gene penetrance functions, permitting an account of the genotype covariate-specific effect on study variables. The results of this study strongly supported the hypothesis of a major gene effect and additional multifactorial component. The best-fitting model was the Mendelian one with an additive type of inheritance. The estimates obtained using the standard three-factor variance decomposition analysis suggest that age (72.8%) and major gene (14.5%) are the main sources of interindividual differences in the development of hand OA. The contribution of the putative major gene on age- and sex-adjusted OA phenotype variation was 55% in the present study.

摘要

本研究的目的是使用大量种族同质的家系样本,调查手部骨关节炎(OA)的遗传程度和模式。研究了两种类型的分离分析(SA)模型。I型模型在进行遗传分析之前,使用针对潜在显著协变量(特别是年龄和性别)进行调整的数据。II型模型将潜在协变量的影响纳入主基因外显率函数中,从而能够考虑基因型协变量对研究变量的特定效应。本研究结果有力地支持了主基因效应和额外多因素成分的假设。最佳拟合模型是具有加性遗传类型的孟德尔模型。使用标准三因素方差分解分析获得的估计值表明,年龄(72.8%)和主基因(14.5%)是手部OA发病个体间差异的主要来源。在本研究中,假定的主基因对年龄和性别调整后的OA表型变异的贡献为55%。

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