Key result
POSTN minor allele A linked to ~72% higher vertebral fracture prevalence versus allele G.
Why the study?
To investigate the association between serum periostin levels, variation in its encoding gene POSTN, vertebral fractures prevalence, and bone mineral density in Chinese postmenopausal women.
Are serum periostin levels and POSTN genetic polymorphisms associated with vertebral fractures and bone mineral density in Chinese postmenopausal women?
Observational (n=385)
Are serum periostin levels and POSTN genetic polymorphisms associated with vertebral fractures and bone mineral density in Chinese postmenopausal women?
Genetic variation in POSTN and serum periostin levels may serve as potential biomarkers for osteoporosis and vertebral fracture risk in Chinese postmenopausal women.
Answers are grounded in this paper and cite their sources.
rs9603226 A allele associated with higher vertebral fracture prevalence; hypothesis-generating for POSTN variants as biomarkers, needing prospective validation.
Purposes: In order to investigate the association between serum periostin levels and the variation of its encoding gene POSTN and the prevalence of vertebral fractures and bone mineral density (BMD) in Chinese postmenopausal women, an association study was performed. Materials and Methods: 385 postmenopausal women were recruited. For participants without a history of vertebral fracture, lateral X-rays of the spine covering the fourth thoracic spine to the fifth lumbar spine were performed to detect any asymptomatic vertebral fractures. Ten tag-single nucleotide polymorphisms (SNP) of POSTN were genotyped. Serum periostin levels, biochemical parameters, and BMD were measured individually. Results: rs9603226 was significantly associated with vertebral fractures. Compared to allele G, the minor allele A carriers of rs9603226 had a 1.722-fold higher prevalence of vertebral fracture (p = 0.037). rs3923854 was significantly associated with the serum periostin level. G/G genotype of rs3923854 had a higher serum periostin level than C/C and C/G (67.26 ± 19.90 ng/mL vs. 54.57 ± 21.44 ng/mL and 54.34 ± 18.23 ng/mL). Furthermore, there was a negative correlation between the serum level of periostin and BMD at trochanter and total hip. Conclusion: Our study suggested that genetic variation of POSTN could be a predicting factor for the risk of vertebral fractures. The serum level of periostin could be a potential biochemical parameter for osteoporosis in Chinese postmenopausal women.
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Guo et al. (2022) conducted an observational in Vertebral fracture and osteoporosis (n=385). POSTN genetic polymorphisms and serum periostin levels vs. Allele G carriers (for rs9603226) was evaluated on Vertebral fractures (1.722-fold higher prevalence, p=0.037). Minor allele A carriers of the POSTN polymorphism rs9603226 had a 1.722-fold higher prevalence of vertebral fracture compared to allele G carriers.
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