首页> 外文期刊>Annals of the Rheumatic Diseases: A Journal of Clinical Rheumatology and Connective Tissue Research >Progression of lumbar disc degeneration over a decade: a heritability study.
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Progression of lumbar disc degeneration over a decade: a heritability study.

机译:十年来腰椎间盘退变的进展:遗传性研究。

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OBJECTIVES: Lumbar disc degeneration (LDD) is prevalent, age-related and contributes to low back pain. Cross-sectional LDD as determined by MRI scan is known to be highly heritable. The authors postulated that the rate of progression might also be controlled by genetic factors. METHODS: A 10-year follow-up of MRI-determined LDD was performed in 234 pairs of twin volunteers in the UK and Australia, comprising 90 monozygotic pairs and 144 dizygotic same-sex twin pairs. Of the total sample, 95% were female. The mean age at baseline was 53.3 years (range 32.3-69.5). The rate of progression was calculated and, because the effect of age was non-linear, the sample was divided into age strata and heritability estimated for each trait's progression. RESULTS: All MRI-determined traits worsened significantly over the period of follow-up (p<0.0001 for each). Change in disc height was not heritable at any age while posterior disc bulge was heritable across all age categories (range 28-53%), with higher heritability in those over 60 years. Change in disc signal intensity and anterior osteophytes were found to be heritable only in those aged under 50 years at baseline (heritability estimates 76% (95% CI 44% to 100%) and 74% (42% to 100%), respectively). CONCLUSIONS: Longitudinal change in LDD traits is heritable for all traits except disc height, but there is a significant influence of age, which varies across traits. Future studies to define the genetic variants influencing LDD progression should examine MRI traits individually and in women should focus on those under 50 years of age.
机译:目的:腰椎间盘退变(LDD)很普遍,与年龄有关,并导致腰痛。通过MRI扫描确定的横截面LDD是高度可遗传的。作者假设进展速度也可能受遗传因素控制。方法:在英国和澳大利亚的234对双生志愿者中进行了MRI确定的LDD的10年随访,包括90对单卵双生和144对同卵双性同性双生。在所有样本中,女性占95%。基线时的平均年龄为53.3岁(范围32.3-69.5)。计算进展速度,并且由于年龄的影响是非线性的,因此将样本分为年龄层次,并针对每个性状的进展估计遗传力。结果:所有MRI确定的特征在随访期间均显着恶化(每个p <0.0001)。在任何年龄段,椎间盘高度的变化都是可遗传的,而在所有年龄段(范围在28-53%之间),椎间盘后凸是可遗传的,在60岁以上人群中,遗传力较高。发现圆盘信号强度和前骨赘的变化仅在基线以下50岁以下的人群中是可遗传的(遗传力估计分别为76%(95%CI为44%至100%)和74%(42%至100%)) 。结论:LDD性状的纵向变化对于除圆盘高度以外的所有性状都是可遗传的,但年龄会产生显着影响,且年龄会因性状而异。未来的研究将确定影响LDD进展的遗传变异,应单独检查MRI特征,女性应关注50岁以下的女性。

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