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腰椎发育性椎管狭窄的家系分析:潜在遗传模式的确定。

Pedigree analysis of lumbar developmental spinal stenosis: Determination of potential inheritance patterns.

机构信息

Department of Orthopaedics and Traumatology, The University of Hong Kong, Pokfulam, Hong Kong SAR, China.

School of Biomedical Sciences, The University of Hong Kong, Pokfulam, Hong Kong SAR, China.

出版信息

J Orthop Res. 2021 Aug;39(8):1763-1776. doi: 10.1002/jor.24850. Epub 2020 Sep 16.

Abstract

Lumbar developmental spinal stenosis (DSS) refers to multilevel pre-existing narrowed spinal canals, which predispose to neural compromise. The objective of this study is to identify any inheritance pattern of DSS by utilizing pedigree charts. This was a case series of 13 families with a total of 80 subjects having magnetic resonance imaging (MRI) from L1 to S1. Cases (subjects with DSS) or controls (subjects without DSS) were identified by measuring their anteroposterior (AP) vertebral canal diameters. Multilevel model analyses were also performed to evaluate whether there is substantial clustering of observations within the families, and the effect of multilevel DSS. The intraclass correlation coefficient (ICC) and Akaike information criteria (AIC) were compared between models. Correlations between subject demographics and AP vertebral canal diameter were statistically insignificant at all levels. Only vertebral canal cross-sectional area, and axial and sagittal vertebral canal diameter were found to be statistically different between cases and controls at all levels (all p < .05). Both males and females were affected by DSS and there was no skipping of generation, which highly suggested DSS followed an autosomal dominant inheritance pattern. After accounting for multilevel DSS, there was a drop of more than 10 in AIC and some variances were also explained within families. This is the first study that suggests multilevel lumbar DSS to have an autosomal dominant inheritance pattern. Within families with a background of DSS, subjects had a smaller canal size, contributed by shortened axial and sagittal AP vertebral canal diameter, and smaller canal cross-sectional area.

摘要

腰椎发育性椎管狭窄症(DSS)是指多节段的椎管先天狭窄,易导致神经受压。本研究的目的是通过绘制家系图来确定 DSS 是否存在遗传模式。这是一项包含 13 个家系共 80 名受试者的病例系列研究,所有受试者均进行了从 L1 到 S1 的磁共振成像(MRI)检查。通过测量其前后(AP)椎管直径来确定病例(DSS 患者)或对照(无 DSS 患者)。还进行了多水平模型分析,以评估家庭内观察值是否存在大量聚类,以及多水平 DSS 的影响。比较了模型之间的组内相关系数(ICC)和赤池信息量准则(AIC)。在所有水平上,受试者人口统计学特征与 AP 椎管直径之间的相关性均无统计学意义。仅在所有水平上发现椎管横截面积、轴向和矢状椎管直径在病例与对照组之间存在统计学差异(均 p<0.05)。男性和女性均受到 DSS 的影响,且没有世代缺失,这强烈表明 DSS 遵循常染色体显性遗传模式。在考虑多水平 DSS 后,AIC 下降了 10 多,并且家庭内的一些方差也得到了解释。这是第一项表明多水平腰椎 DSS 具有常染色体显性遗传模式的研究。在具有 DSS 背景的家庭中,由于轴向和矢状 AP 椎管直径缩短以及椎管横截面积较小,导致受试者椎管较小。

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