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遗传因素对颈椎和腰椎间盘退变的影响:一项双胞胎的磁共振成像研究

Genetic influences on cervical and lumbar disc degeneration: a magnetic resonance imaging study in twins.

作者信息

Sambrook P N, MacGregor A J, Spector T D

机构信息

University of Sydney, Royal North Shore Hospital, St. Leonards, Australia.

出版信息

Arthritis Rheum. 1999 Feb;42(2):366-72. doi: 10.1002/1529-0131(199902)42:2<366::AID-ANR20>3.0.CO;2-6.

Abstract

OBJECTIVE

Degenerative intervertebral disc disease is common; however, the importance of genetic factors is unknown. This study sought to determine the extent of genetic influences on disc degeneration by classic twin study methods using magnetic resonance imaging (MRI).

METHODS

We compared MRI features of degenerative disc disease in the cervical and lumbar spine of 172 monozygotic and 154 dizygotic twins (mean age 51.7 and 54.4, respectively) who were unselected for back pain or disc disease. An overall score for disc degeneration was calculated as the sum of the grades for disc height, bulge, osteophytosis, and signal intensity at each level. A "severe disease" score (excluding minor grades) and an "extent of disease" score (number of levels affected) were also calculated.

RESULTS

For the overall score, heritability was 74% (95% confidence interval [95% CI] 64-81%) at the lumbar spine and 73% (95% CI 64-80%) at the cervical spine. For "severe disease," heritability was 64% and 79% at the lumbar and cervical spine, respectively, and for "extent of disease," heritability was 63% and 63%, respectively. These results were adjusted for age, weight, height, smoking, occupational manual work, and exercise. Examination of individual features revealed that disc height and bulge were highly heritable at both sites, and osteophytes were heritable in the lumbar spine.

CONCLUSION

These results suggest an important genetic influence on variation in intervertebral disc degeneration. However, variation in disc signal is largely influenced by environmental factors shared by twins. The use of MRI scans to determine the phenotype in family and population studies should allow a better understanding of disease mechanisms and the identification of the genes involved.

摘要

目的

退行性椎间盘疾病很常见;然而,遗传因素的重要性尚不清楚。本研究旨在通过使用磁共振成像(MRI)的经典双生子研究方法来确定遗传因素对椎间盘退变的影响程度。

方法

我们比较了172对同卵双胞胎和154对异卵双胞胎(平均年龄分别为51.7岁和54.4岁)颈椎和腰椎的退行性椎间盘疾病的MRI特征,这些双胞胎未因背痛或椎间盘疾病而被挑选。椎间盘退变的总体评分计算为每个节段椎间盘高度、膨出、骨赘形成和信号强度等级的总和。还计算了“严重疾病”评分(不包括轻微等级)和“疾病范围”评分(受影响的节段数)。

结果

对于总体评分,腰椎的遗传度为74%(95%置信区间[95%CI]64 - 81%),颈椎为73%(95%CI 64 - 80%)。对于“严重疾病”,腰椎和颈椎的遗传度分别为64%和79%,对于“疾病范围”,遗传度分别为63%和63%。这些结果针对年龄、体重、身高、吸烟、职业体力劳动和运动进行了调整。对个体特征的检查显示,椎间盘高度和膨出在两个部位都具有高度遗传性,腰椎的骨赘具有遗传性。

结论

这些结果表明遗传因素对椎间盘退变的变异有重要影响。然而,椎间盘信号的变异在很大程度上受双胞胎共有的环境因素影响。在家庭和人群研究中使用MRI扫描来确定表型应有助于更好地理解疾病机制并识别相关基因。

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