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寻找手部骨关节炎与11号染色体q12 - 13区段之间的连锁关系。

Search for linkage between hand osteoarthritis and 11q 12-13 chromosomal segment.

作者信息

Kalichman L, Kobyliansky E, Malkin I, Yakovenko K, Livshits G

机构信息

Human Population Biology Research Unit, Department of Anatomy and Anthropology, Sackler Faculty of Medicine, Tel Aviv University, Ramat Aviv, 69978, Tel Aviv, Israel.

出版信息

Osteoarthritis Cartilage. 2003 Aug;11(8):561-8. doi: 10.1016/s1063-4584(03)00093-1.

Abstract

OBJECTIVE

The aims of the present study were: (1) to evaluate the extent and mode of inheritance of hand osteoarthritis by using a large sample of ethnically homogeneous pedigrees of Caucasian origin; (2) to examine whether the synthetic measure of osteoarthritis according to Kellgren and Lawrence (K-L) and the more specific measure, namely, the extent of osteophytes development, have a similar putative genetic determination and pattern of biological inheritance and (3) to test the hypothesis that hand osteoarthritis dependent phenotypes are linked to the 11q 12-13 chromosomal region.

METHODS

The population of the present study comprised 1190 Chuvashians (Russian Federation) belonging to 295 nuclear families. Segregation analysis was carried out on a total sample. Sub-sample of 571 individuals was used to conduct Transmission/disequilibrium test (TDT) and model-based linkage analysis.

RESULTS

Adjusted for age, sex and other covariates, both OA phenotypes showed significant familial aggregation. The model fitting analysis strongly supported the hypothesis of a major gene effect on study traits. The inferred major gene explained about 52% of the osteophyte score (OPS) and 49% of the K-L score variation adjusted for confounding variables. The series of model-based linkage analyses and TDTs provided inconclusive evidence on possible linkage of both phenotypes to the 11q 12-13 chromosomal region.

CONCLUSIONS

We support the hypothesis of a major gene effect in heritability of hand osteoarthritis in both phenotypes. Despite the fact that some DNA markers showed statistically significant association to studied primary phenotypes, we find only weak evidence of linkage disequilibrium between hand osteoarthritis and the proximal part of the 11q 12-13 chromosomal segment (D11S1983 for K-L score and D11S1313 for OPS). The subject, however, a merit requires further investigation.

摘要

目的

本研究的目的如下:(1)通过使用大量来自白种人、种族同质的家系样本,评估手部骨关节炎的遗传程度和模式;(2)检验根据凯尔格伦和劳伦斯(K-L)制定的骨关节炎综合测量方法以及更具体的测量方法,即骨赘形成程度,是否具有相似的假定遗传决定因素和生物学遗传模式;(3)检验手部骨关节炎相关表型与11q 12 - 13染色体区域相关的假设。

方法

本研究的人群包括来自295个核心家庭的1190名楚瓦什人(俄罗斯联邦)。对整个样本进行分离分析。使用571名个体的子样本进行传递/不平衡检验(TDT)和基于模型的连锁分析。

结果

在对年龄、性别和其他协变量进行调整后,两种骨关节炎表型均显示出显著的家族聚集性。模型拟合分析有力地支持了存在影响研究性状的主基因效应这一假设。推断的主基因解释了经混杂变量调整后的骨赘评分(OPS)变异的约52%以及K-L评分变异的49%。一系列基于模型的连锁分析和TDT未能提供确凿证据证明两种表型与11q 12 - 13染色体区域存在可能的连锁关系。

结论

我们支持主基因效应在两种表型的手部骨关节炎遗传中起作用这一假设。尽管一些DNA标记显示与所研究的主要表型存在统计学上的显著关联,但我们仅发现手部骨关节炎与11q 12 - 13染色体片段近端部分(K-L评分对应的D11S1983和OPS对应的D11S1313)之间存在弱的连锁不平衡证据。然而,该课题值得进一步研究。

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