Association of COL2A1rs2276454, rs1793953, COL9A1rs1135056, COL11A1rs1676486 structure-forming collagens of the nucleus pulposus with degeneration of intervertebral discs L5-L4, L5-S1

IF 0.1 Q4 PATHOLOGY
Ye. H. Pedachenko, I. H. Vasylieva, M. Khyzhniak, O. S. Halanta, N. Chopyk, O. Tsiubko, A. B. Hriazov, O. Nekhlopochyn, T. A. Ksenzov, A. Dmytrenko, T. Makarova
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引用次数: 0

Abstract

Aim. The purpose of the work was to determine the relationship between degenerative changes of the L5-S1 and L4-L5 intervertebral discs with collagen mononucleotide variants COL2A1rs2276454, rs1793953, COL9A1rs1135056, COL11A1rs1676486 among ethnic Ukrainians. Materials and methods. The following subjects were investigated: 90 persons of the case group with degeneration of the intervertebral disc L5-S1; 50 persons of the case group with degeneration of the intervertebral disc L4-L5; 66 people of the control group. The object of the study was the venous blood of patients with degenerative lesions of the intervertebral discs and healthy donors. Venous blood was obtained as a result of venipuncture. Typing of COL2A1rs2276454, COL2A1rs1793953, COL9A1rs1135056, COL11A1rs1676486 was performed using the Tag Man Universal PCR Master Mix kit (Applied Biosystems, USA) and Tag Man SNP Genotyping Assays for the determination of polymorphisms (Applied Biosystems, USA). The research was carried out by specialists in the field of molecular biology and biochemistry of the Department of Neurobiochemistry of the SI “Romodanov Neurosurgery Institute, National Academy of Medical Sciences of Ukraine”, using the CFX96 device (Bio-Rrad, USA). Certificate of determination of measuring capabilities No. PT-322/21 from 07/28/2021 to 08/27/2023. Results. COL2A1rs2276454 may have a protective value for the development of degeneration of the intervertebral disc L5-S1 among men (OR (95 % CI): 0.27 (0.10–0.80), χ2 = 6.02, P = 0.015). Genotype C/T (COL9A1rs1135056) is 3.25 times more common among male patients with degeneration of the intervertebral disc L5-S1 in comparison with the female case group (OR (95 % CI): 3.25 (1.20–8.84), χ2 = 5.50, P = 0.02). The presence of the genotype G/A (COL11A1rs1676486) in the general group of patients with degeneration of the intervertebral disc L5-S1 is observed 5.46 times more often among male patients (OR (95 % CI): 5.46 (1.60–18.47), χ2 = 8.29, P = 0.004); G/A is registered 4.17 times more often among men compared to the group of women (OR (95 % CI): 4.17 (1.070–16.82), χ2 = 4.17, P = 0.04). Comparison of the odds of observing the genotype G/G, G/A, AA in the group of men with degeneration of the intervertebral disc L5-S1 showed a statistically significant 4.06 times predominance of the genotype G/A (OR (95 % CI): 4.06 (1.23–13.38), χ2 = 4.17, P = 0.04). The most probable model of heredity for COL11A1rs1676486 is dominant OR (95 % CI): 2.08 (1.03–4.21), χ2 = 4.26, P = 0.04. Associations of COL2A1rs2276454, rs1793953, COL9A1rs1135056, COL11A1rs1676486 structure-forming collagens of the gelatinous nucleus with degeneration of L5-L4 intervertebral discs were not detected. Conclusions. The COL2A1rs2276454 may be protective for the development of L5-S1 intervertebral disc degeneration in men (OR (95 % CI): 0.27 (0.10–0.80), χ2 = 6.02, Р = 0.015). COL2A1rs1793953 is not associated with degeneration of intervertebral discs L4-L5, L5-S1. С/T COL9A3rs1135056 genotype is associated with L5-S1 intervertebral disc degeneration among males (OR (95 % CI): 3.25 (1.20–8.84), χ2 = 5.50, Р = 0.02) compared with L5-S1 females. G/A COL11A1rs1676486 genotype is associated with L5-S1 intervertebral disc degeneration among male patients (OR (95 % CI): 5.46 (1.60–18.47), χ2 = 8.29, Р = 0.004) and compared to female patients (OR (95 % CI): 4.17 (1.07–16.82), χ2 = 4.17, Р = 0.04). The type of inheritance COL11A1rs1676486 is dominant.  
COL2A1rs2276454, rs1793953, COL9A1rs1135056, COL11A1rs1676486髓核结构形成胶原与L5-L4, L5-S1椎间盘退变的关系
的目标。本研究的目的是确定乌克兰人L5-S1和L4-L5椎间盘退行性改变与胶原单核苷酸变异COL2A1rs2276454、rs1793953、COL9A1rs1135056、COL11A1rs1676486之间的关系。材料和方法。以下受试者被调查:病例组中有90人患有L5-S1椎间盘退变;L4-L5椎间盘退变病例组50例;对照组的66人。本研究的对象是椎间盘退行性病变患者和健康供者的静脉血。静脉穿刺获得静脉血。COL2A1rs2276454、COL2A1rs1793953、COL9A1rs1135056、COL11A1rs1676486的分型采用Tag Man Universal PCR Master Mix kit (Applied Biosystems, USA)和Tag Man SNP基因分型测定(Applied Biosystems, USA)。该研究由“乌克兰国家医学科学院罗莫达诺夫神经外科研究所”SI神经生物化学系分子生物学和生物化学领域的专家使用CFX96装置(Bio-Rrad,美国)进行。测量能力确定证书PT-322/21从2021年7月28日至2023年8月27日。COL2A1rs2276454可能对男性L5-S1椎间盘退变的发生有保护作用(OR (95% CI): 0.27 (0.10-0.80), χ2 = 6.02, P = 0.015)。基因型C/T (COL9A1rs1135056)在男性L5-S1椎间盘退变患者中的发生率是女性病例组的3.25倍(OR (95% CI): 3.25 (1.20 ~ 8.84), χ2 = 5.50, P = 0.02)。G/A (COL11A1rs1676486)基因型在普通组L5-S1椎间盘退变患者中出现的频率是男性患者的5.46倍(95% CI: 5.46 (1.60 ~ 18.47), χ2 = 8.29, P = 0.004);男性的G/A发生率是女性的4.17倍(OR (95% CI): 4.17 (1.070-16.82), χ2 = 4.17, P = 0.04)。男性椎间盘退变L5-S1组G/G、G/A、AA基因型优势率比较,G/A基因型优势率为4.06倍,差异有统计学意义(95% CI: 4.06 (1.23 ~ 13.38), χ2 = 4.17, P = 0.04)。COL11A1rs1676486最可能的遗传模式为显性OR (95% CI): 2.08 (1.03 ~ 4.21), χ2 = 4.26, P = 0.04。未发现COL2A1rs2276454、rs1793953、COL9A1rs1135056、COL11A1rs1676486胶质核结构形成胶原与L5-L4椎间盘退变的相关性。COL2A1rs2276454可能对男性L5-S1椎间盘退变的发生有保护作用(OR (95% CI): 0.27 (0.10-0.80), χ2 = 6.02, Р = 0.015)。COL2A1rs1793953与L4-L5、L5-S1椎间盘退变无关。С/T COL9A3rs1135056基因型与L5-S1椎间盘退变相关(OR (95% CI): 3.25 (1.20-8.84), χ2 = 5.50, Р = 0.02)。G/A COL11A1rs1676486基因型与男性患者L5-S1椎间盘退变相关(OR (95% CI): 5.46 (1.60-18.47), χ2 = 8.29, Р = 0.004),与女性患者相比(OR (95% CI): 4.17 (1.07-16.82), χ2 = 4.17, Р = 0.04)。遗传类型COL11A1rs1676486占主导地位。
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来源期刊
Pathologia
Pathologia PATHOLOGY-
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