Genetic predisposition of BMP7 polymorphisms to lumbar disk herniation in the Chinese Han population

• Published in: Cell cycle (Georgetown, Tex.) Vol. 23; no. 4; pp. 466 - 477
• Main Authors: Sun, Kai, Liu, Ruiyu
• Format: Journal Article
• Language: English
• Published: United States Taylor & Francis 16.02.2024
• Subjects: Adult; Aged; Asian People - genetics; BMP7 polymorphisms; Bone Morphogenetic Protein 7 - genetics; Case-Control Studies; China; East Asian People; Female; Genetic Predisposition to Disease - genetics; Humans; Intervertebral Disc Displacement - genetics; Lumbar disk herniation; Lumbar Vertebrae - pathology; Male; Middle Aged; Polymorphism, Single Nucleotide - genetics; Research Paper; Risk Factors; China; Lumbar disk herniation; BMP7 polymorphisms; risk factors
• ISSN: 1538-4101; 1551-4005; 1551-4005
• DOI: 10.1080/15384101.2024.2342703

Bone morphogenetic protein 7 (BMP7) can induce skeletal formation, promote the differentiation of chondrocytes and osteoblasts, and ameliorate intervertebral disc degeneration. The study was designed to evaluate the relationship of BMP7 variants to LDH risk in the Chinese Han population. BMP7 variants were genotyped with the Agena MassARRAY system among 690 LDH patients and 690 healthy controls. The odds ratio (OR) and 95% confidence interval (CI) were calculated by logistic regression. Multi-factor dimension reduction (MDR) (version 3.0.2) software was used to evaluate the effect of BMP7 variant-variant interaction on the susceptibility to LDH. Here, the risk-reducing association between rs230189 and LDH occurrence was found (p = 0.005, OR = 0.79). Specially, rs230189 was associated with decreased LDH risk in females (p = 0.001, OR = 0.60), elder group (p = 0.025, OR = 0.76), subjects with BMI < 24 kg/m 2 (p = 0.027, OR = 0.48), nonsmokers (p = 0.001, OR = 0.66), and nondrinkers (p = 0.011, OR = 0.72). Moreover, rs1321862 might be the risk factor for LDH susceptibility among the participants with BMI < 24 kg/m 2 (p = 0.024, OR = 1.84). MDR results displayed that rs230189 was the greatest attribution factor on LDH risk in the single-locus model, with an information gain of 0.44%. The present study demonstrated that BMP7 rs230189 g.55771443A>C may play a protective role against LDH risk. Our findings may help to understand the potential mechanism of BMP7 in LDH susceptibility.