Rajasekaran S, Kanna Rishi Mugesh, Senthil Natesan, Raveendran Muthuraja, Ranjani Veera, Cheung Kenneth M C, Chan Danny, Kao Patrick Y P, Yee Anita, Shetty Ajoy Prasad
Department of Orthopaedics and Spine Surgery, Ganga Hospital, 313, Mettupalayam Road, Coimbatore, Tamil Nadu, 641 011, India,
Eur Spine J. 2015 Sep;24(9):1969-75. doi: 10.1007/s00586-014-3687-y. Epub 2014 Nov 22.
Although the exact mechanisms that lead to degenerative disc disease (DDD) are not well understood, a significant genetic influence has been found. Focusing on DDD that occurs in young adults can be valuable in determining the exact role of genetic predisposition to DDD.
Patients (<40 years) with lumbar disc degeneration were evaluated with MRI imaging (1.5 Tesla) and genetic association analysis for 58 single nucleotide polymorphism (SNP) of 35 candidate genes was performed. Disc degeneration of individual discs of lumbar spine from L1 to S1 was graded by Pfirrmann's grading. The subjects were stratified into two groups based on Total Disc Degenerative Score (TDDS). Based on TDDS, the severity of DDD was classified as mild (Group A: TDDS <10) and severe (Group B: TDDS >10).
695 Indian subjects including 308 with mild TDDS and 387 with severe TDDS were studied. The mean age of the patients was 29.6 ± 6.9 years in group A and 31.7 ± 6.1 in group B (p < 0.05). Five of the 35 candidate genes viz., rs1337185 of COL11A (p = 0.02), rs5275 (p = 0.03) and rs5277 (p = 0.05) of COX2, rs7575934 of IL1F5 (p = 0.04), rs3213718 of CALM1 (p = 0.04) and rs162509 of ADAMTS5 (p = 0.04) were found to be significantly associated with severe TDDS.
The study identifies specific SNP associations of five genes in young adults with severe lumbar disc degeneration. These five genes (COL11A1, ADAMTS5, CALM1, IL1F5 and COX2) have different functions in the matrix metabolism, intracellular signalling and inflammatory cascade. This shows that disc degeneration is a complex disease with an intricate interplay of multiple genetic polymorphisms.
尽管导致椎间盘退变(DDD)的确切机制尚未完全明确,但已发现其受显著的遗传影响。关注发生于年轻人的DDD对于确定遗传易感性在DDD中的确切作用具有重要价值。
对年龄小于40岁的腰椎间盘退变患者进行1.5特斯拉的MRI成像评估,并对35个候选基因的58个单核苷酸多态性(SNP)进行基因关联分析。根据Pfirrmann分级对腰椎从L1至S1各节段椎间盘退变情况进行分级。根据椎间盘退变总分(TDDS)将研究对象分为两组。基于TDDS,将DDD的严重程度分为轻度(A组:TDDS<10)和重度(B组:TDDS>10)。
共研究了695名印度受试者,其中308名TDDS轻度患者,387名TDDS重度患者。A组患者的平均年龄为29.6±6.9岁,B组为31.7±6.1岁(p<0.05)。35个候选基因中的5个,即COL11A的rs1337185(p = 0.02)、COX2的rs5275(p = 0.03)和rs5277(p = 0.05)、IL1F5的rs7575934(p = 0.04)、CALM1的rs3213718(p = 0.04)以及ADAMTS5的rs162509(p = 0.04),被发现与重度TDDS显著相关。
该研究确定了与重度腰椎间盘退变的年轻成年人中五个基因的特定SNP关联。这五个基因(COL11A1、ADAMTS5、CALM1、IL1F5和COX2)在基质代谢、细胞内信号传导和炎症级联反应中具有不同功能。这表明椎间盘退变是一种复杂疾病,由多种基因多态性相互作用所致。