|
rs10998461
|
|
|
0.010 |
GeneticVariation |
BEFREE |
In the haplotype analysis, the haplotype "GT" in block (rs10998461 and rs10998468) decreased LDH risk (OR = 0.7, 95% CI = 0.52-0.93, p = .016).
|
31724315 |
2020 |
|
rs10998468
|
|
|
0.010 |
GeneticVariation |
BEFREE |
In the haplotype analysis, the haplotype "GT" in block (rs10998461 and rs10998468) decreased LDH risk (OR = 0.7, 95% CI = 0.52-0.93, p = .016).
|
31724315 |
2020 |
|
rs4472827
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Our results provide evidence for polymorphisms of rs7903209 and rs4472827 in STOX1 associated with LDH risk in Chinese Han population.
|
31724315 |
2020 |
|
rs7903209
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Our results provide evidence for polymorphisms of rs7903209 and rs4472827 in STOX1 associated with LDH risk in Chinese Han population.
|
31724315 |
2020 |
|
rs10490571
|
|
|
0.010 |
GeneticVariation |
BEFREE |
In addition, the recessive model (CT/CC versus TT, OR=3.43, 95% CI: 1.11-10.57, P=0.020) of rs10490571 was associated with an increased LDH risk among people older than 50 years of age.
|
31104063 |
2019 |
|
rs62413038
|
|
|
0.010 |
GeneticVariation |
BEFREE |
We found that the minor alleles of rs62413038 (OR = 1.21, 95%CI: 1.01-1.43, p = .036) and rs9450607 (OR = 1.26, 95% CI: 1.05-1.53, p = .016) were associated with an increased risk of lumbar disc herniation in the allelic model analysis.
|
31359629 |
2019 |
|
rs8040868
|
|
|
0.010 |
GeneticVariation |
BEFREE |
We found that the individuals with rs8040868 CT genotype had a 0.46-fold higher risk of lumba</span>r disc herniation than those with rs8040868 TT genotype, in men group (OR = 0.46, 95% CI 0.25-0.84, p = 0.012).
|
31362771 |
2019 |
|
rs9450607
|
|
|
0.010 |
GeneticVariation |
BEFREE |
We found that the minor alleles of rs62413038 (OR = 1.21, 95%CI: 1.01-1.43, p = .036) and rs9450607 (OR = 1.26, 95% CI: 1.05-1.53, p = .016) were associated with an increased risk of lumbar disc herniation in the allelic model analysis.
|
31359629 |
2019 |
|
rs956730
|
|
|
0.010 |
GeneticVariation |
BEFREE |
RESULTS The mutant homozygous genotype in codominant model (AA versus GG, OR=2.37, 95% CI: 1.08-5.21, P=0.001) and in recessive model (AA versus GG/GA, OR=2.82, 95% CI: 1.30-6.12, P=0.005) of rs956730 were associated with an increased LDH risk in males, while rs956730 heterozygous genotype under codominant model (AG versus GG, OR=0.65, 95% CI: 0.46-0.92, P=0.001) was a protective genotype in males.
|
31104063 |
2019 |
|
rs10767664
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Rs11030064 in BDNFOS gene was associated with modified susceptibility for LDH at age ≤50 years but three loci (rs6265, rs11030104 and rs10767664) of BDNF gene increased LDH risk at age >50 years.
|
30143695 |
2018 |
|
rs11030064
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Haplotype analysis shown that haplotype "GCC" in the block (rs988712, rs7481311, and rs11030064) increased LDH risk (OR = 1.49, 95% CI = 1.06-2.10, p = 0.022) at age ≤50 years.
|
30143695 |
2018 |
|
rs11030096
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Further, rs11030096 polymorphism in BDNFOS gene was associated with LDH the increased susceptibility of LDH in females.
|
30143695 |
2018 |
|
rs11030104
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Rs11030064 in BDNFOS gene was associated with modified susceptibility for LDH at age ≤50 years but three loci (rs6265, rs11030104 and rs10767664) of BDNF gene increased LDH risk at age >50 years.
|
30143695 |
2018 |
|
rs11066028
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Additionally, the haplotype "GGCTCACG" constructed by rs886205, rs2238152, rs4648328, rs441, rs4646778, rs671, rs11066028, and rs7296651 was associated with increased risk of LDH (OR = 1.45; 95% CI = 1.11-1.90; P = 0.0071).
|
30166580 |
2018 |
|
rs45437897
|
|
|
0.010 |
GeneticVariation |
BEFREE |
The SNP rs17576 was found to be significantly associated with susceptibility to LDH (OR = 0.77, p = 0.0002), which was also confirmed by haplotype-based analyses (rs79845319-rs17576-rs45437897, global p < 0.001).
|
30289281 |
2018 |
|
rs4633
|
|
|
0.010 |
GeneticVariation |
BEFREE |
We have identified a significant SNP of COMT, rs4633, which is associated with symptomatic LDH in a large Chinese Han-based sample of the study subjects.
|
30158547 |
2018 |
|
rs6265
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Rs11030064 in BDNFOS gene was associated with modified susceptibility for LDH at age ≤50 years but three loci (rs6265, rs11030104 and rs10767664) of BDNF gene increased LDH risk at age >50 years.
|
30143695 |
2018 |
|
rs671
|
|
|
0.010 |
GeneticVariation |
BEFREE |
In the allele model analysis, we found the frequency of the "A" allele of rs671 was significantly higher in LDH cases than in controls (OR = 1.414, 95%CI: 1.109-1.803, P = 0.005).
|
30166580 |
2018 |
|
rs7296651
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Additionally, the haplotype "GGCTCACG" constructed by rs886205, rs2238152, rs4648328, rs441, rs4646778, rs671, rs11066028, and rs7296651 was associated with increased risk of LDH (OR = 1.45; 95% CI = 1.11-1.90; P = 0.0071).
|
30166580 |
2018 |
|
rs7481311
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Haplotype analysis shown that haplotype "GCC" in the block (rs988712, rs7481311, and rs11030064) increased LDH risk (OR = 1.49, 95% CI = 1.06-2.10, p = 0.022) at age ≤50 years.
|
30143695 |
2018 |
|
rs79845319
|
|
|
0.010 |
GeneticVariation |
BEFREE |
The SNP rs17576 was found to be significantly associated with susceptibility to LDH (OR = 0.77, p = 0.0002), which was also confirmed by haplotype-based analyses (rs79845319-rs17576-rs45437897, global p < 0.001).
|
30289281 |
2018 |
|
rs886205
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Additionally, the haplotype "GGCTCACG" constructed by rs886205, rs2238152, rs4648328, rs441, rs4646778, rs671, rs11066028, and rs7296651 was associated with increased risk of LDH (OR = 1.45; 95% CI = 1.11-1.90; P = 0.0071).
|
30166580 |
2018 |
|
rs143383
|
|
|
0.010 |
GeneticVariation |
BEFREE |
The aim of the present study is to assess whether the single nucleotide polymorphism in the GDF5 (+104T/C; rs143383) is associated with the symptomatic lumbar disc herniation in the Chinese Han population and the identification of the mechanisms of its action.
|
24105021 |
2014 |
|
rs2615977
|
|
|
0.010 |
GeneticVariation |
BEFREE |
This corresponded with observations in LDH but the SNP was not associated with OA.We did not observe AEI at rs2615977.
|
23497244 |
2013 |
|
rs1799971
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Pain intensity the first year after lumbar disc herniation is associated with the A118G polymorphism in the opioid receptor mu 1 gene: evidence of a sex and genotype interaction.
|
22815498 |
2012 |