Chinese Journal of Tissue Engineering Research ›› 2020, Vol. 24 ›› Issue (32): 5128-5132.doi: 10.3969/j.issn.2095-4344.2860

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Association of HTRA1 and HAPLN1 gene polymorphism with intervertebral disc degeneration

Yang Jinfeng, Ma Sanhui   

  1. Department of Orthopedics, People’s Hospital of Dingzhou, Dingzhou 073000, Hebei Province, China
  • Received:2019-09-10 Revised:2019-09-12 Accepted:2019-12-05 Online:2020-11-18 Published:2020-09-24
  • About author:Yang Jinfeng, Attending physician, Department of Orthopedics, People’s Hospital of Dingzhou, Dingzhou 073000, Hebei Province, China
  • Supported by:

    the Scientific Research Foundation of Hebei Provincial Health Department, No. 20181772

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Abstract:

BACKGROUND: Studies have found that single nucleotide polymorphism genotypes in the HTRA1 gene promoter region are associated with intervertebral disc degeneration, while HAPLN1 is associated with osteoarthritis caused by intervertebral disc degeneration.

OBJECTIVE: To explore the role of human secretory serine protease HTRA1 and the key group of extracellular matrix HAPLN1 in the pathogenesis of intervertebral disc degeneration.

METHODS: This study included 498 postmenopausal female subjects who underwent a physical examination at Dingzhou People’s Hospital from April 2015 to December 2018. TaqMan PCR was used to detect HTRA1 gene promoter rs11200638 single nucleotide polymorphism and HAPLN1 gene 5' flanking rs975563, intron 1 rs10942332, intron 2 rs179851 and intron 4 rs4703570 single nucleotide polymorphism in 498 postmenopausal Chinese women. The correlation between the HTRA1orHAPLN1 gene polymorphisms and the radiographic features of spinal disc degeneration was analyzed. The trial has been approved by the Ethics Committee of Dingzhou People’s Hospital.

RESULTS AND CONCLUSION: Among the 498 subjects with the HTRA1 gene rs11200638 single nucleotide polymorphism, 178 were GG homozygotes, 222 were GA heterozygotes, and 98 were AA homozygotes. We compared the parameters of intervertebral disc degeneration in subjects with at least one G allele (GG+GA, n=400) and without G allele (AA, n=98). In HTRA1 gene rs11200638 single nucleotide polymorphism, the score on intervertebral space stenosis in the subjects with GG+GA allele genome was lower than that in the subjects with AA allele (P < 0.001). With the increase of the score on intervertebral space stenosis, the proportion of the subjects with AA alleles increased (P ≤ 0.001). Among the 498 subjects with single nucleotide polymorphisms of the HAPLN1 gene, 137 were homozygous for TT, 230 were heterozygous for CT, and 131 were homozygous for CC. Intervertebral disc degeneration parameters of CC+TT allele (n=361) and TT allele (n=137) were compared. In the HAPLN1 gene, there was a significant difference between the CC+TT and TT alleles of the rs179851 single nucleotide polymorphism in osteophyte formation and intervertebral space stenosis (P < 0.01). Among the HAPLN1 gene rs179851 single nucleotide polymorphisms, the proportion of subjects with TT alleles and intervertebral space stenosis ≥ 6 points increased (P < 0.05). With an increase in osteophyte formation score, the proportion of subjects with TT allele increased (P < 0.001). These results reveal that HTRA1 and HAPLN1 genetic variations at specific genetic loci are associated with intervertebral disc degeneration.

Key words: ">single nucleotide polymorphism, high temperature requirement serine protease A1 (HTRA1), hyaluronan and proteoglycan link protein 1 (HAPLN1), intervertebral disc degeneration, genetic variation, allele, osteophyte formation, intervertebral space stenosis

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