Solovieva Svetlana, Lohiniva Jaana, Leino-Arjas Päivi, Raininko Raili, Luoma Katariina, Ala-Kokko Leena, Riihimäki Hilkka
Department of Epidemiology and Biostatistics, Finnish Institute of Occupational Health, Helsinki, Finland.
Spine (Phila Pa 1976). 2002 Dec 1;27(23):2691-6. doi: 10.1097/00007632-200212010-00008.
Cross-sectional.
To evaluate the interaction between the COL9A3 gene polymorphism and persistent obesity in relation to lumbar disc degeneration.
Obesity has been suggested to be a risk factor for disc degeneration. There is some indication for an association between collagen IX genes and lumbar disc disease characterized by sciatica. However, the interaction between those factors in their influences on the risk of disc degeneration has not been studied.
Blood samples from 135 middle-aged men who had undergone magnetic resonance imaging (MRI) of the lumbar spine were analyzed for the presence of an arginine to tryptophan change in the COL9A3 gene (Trp3 allele). The men represented three occupations: 41 were machine drivers, 42 were carpenters, and 52 were office workers. The discs L2/L3-L5/S1 were evaluated on MRI, using decreased signal intensity of the nucleus pulposus, posterior disc bulges, and decreased disc height as signs of disc degeneration. Based on self-reports on body height and weight currently and at the age of 25 years, obesity history was classified as no obesity, persistent obesity, and other. Rothman's synergy index was used as a measure of interaction between two factors.
The Trp3 allele and persistent obesity acted synergistically to increase the risk of dark nucleus pulposus, posterior disc bulge, and decreased disc height at L4/L5; of multilevel posterior disc bulges; and of decreased disc height. From 45% to 71% of disc degeneration among persistently obese individuals with the Trp3 allele could be attributed to the synergism of these two factors.
The effect of obesity on lumbar disc degeneration seems to be modified by the collagen IX gene polymorphism, so that people who carry the Trp3 allele are at increased risk if they are persistently obese.
横断面研究。
评估COL9A3基因多态性与持续性肥胖在腰椎间盘退变方面的相互作用。
肥胖被认为是椎间盘退变的一个危险因素。有迹象表明,IX型胶原蛋白基因与以坐骨神经痛为特征的腰椎疾病之间存在关联。然而,这些因素在影响椎间盘退变风险方面的相互作用尚未得到研究。
对135名接受过腰椎磁共振成像(MRI)检查的中年男性的血液样本进行分析,以检测COL9A3基因中精氨酸到色氨酸的变化(Trp3等位基因)。这些男性代表三种职业:41名是机器驾驶员,42名是木匠,52名是办公室职员。在MRI上评估L2/L3至L5/S1椎间盘,以髓核信号强度降低、椎间盘后凸和椎间盘高度降低作为椎间盘退变的征象。根据目前和25岁时的身高和体重自我报告,肥胖史分为无肥胖、持续性肥胖和其他。采用Rothman协同指数作为两个因素之间相互作用的衡量指标。
Trp3等位基因与持续性肥胖协同作用,增加了L4/L5节段出现暗髓核、椎间盘后凸和椎间盘高度降低的风险;多节段椎间盘后凸的风险;以及椎间盘高度降低的风险。在携带Trp3等位基因的持续性肥胖个体中,45%至71%的椎间盘退变可归因于这两个因素的协同作用。
肥胖对腰椎间盘退变的影响似乎因IX型胶原蛋白基因多态性而改变,因此携带Trp3等位基因的人如果持续肥胖,风险会增加。