The role of ADAMTS6 and ADAMTS17 polymorphisms in susceptibility to lumbar disc herniation in Chinese Han population
Purpose LDH caused by lumbar disc degeneration is associated with genetic factors. However, the role of ADAMTS6 and ADAMTS17 genes in LDH risk is still unknown. Methods To investigate the interaction between ADAMTS6 and ADAMTS17 variants in the susceptibility of LDH, five SNPs were genotyped in 509...
Gespeichert in:
Veröffentlicht in: | European spine journal 2023-04, Vol.32 (4), p.1106-1114 |
---|---|
Hauptverfasser: | , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | Purpose
LDH caused by lumbar disc degeneration is associated with genetic factors. However, the role of
ADAMTS6
and
ADAMTS17
genes in LDH risk is still unknown.
Methods
To investigate the interaction between
ADAMTS6
and
ADAMTS17
variants in the susceptibility of LDH, five SNPs were genotyped in 509 patients and 510 healthy individuals. The experiment used logistic regression to calculate odds ratio (OR) and 95% confidence interval (CI). Multi-factor dimensionality reduction (MDR) was chosen to evaluate impact of interaction of SNP-SNP on susceptibility to LDH.
Results
ADAMTS17
-rs4533267 is significantly associated with reducing risk of LDH (OR = 0.72, 95% CI = 0.57–0.9
0, p
= 0.005). Stratified analysis indicates that
ADAMTS17
-rs4533267 is significantly associated with the reducing risk of LDH among participants aged ≤ 48 years old. In addition, we observed that
ADAMTS6
-rs2307121 was associated with increasing risk of LDH in females. MDR analysis shows that single-locus model composed by
ADAMTS17
-rs4533267 can be chosen as the best model for predicting susceptibility to LDH (CVC = 10/10, test accuracy = 0.543).
Conclusion
ADAMTS6
-rs2307121 and
ADAMTS17
-rs4533267 are potentially associated with LDH susceptibility. In particular,
ADAMTS17
-rs4533267 has a strong association with reducing risk of LDH. |
---|---|
ISSN: | 0940-6719 1432-0932 |
DOI: | 10.1007/s00586-023-07586-8 |