Apoptosis-related Fas and FasL gene polymorphisms’ associations with knee osteoarthritis

2013 ◽  
Vol 33 (8) ◽  
pp. 2039-2043 ◽  
Author(s):  
Melek Sezgin ◽  
İbrahim Ömer Barlas ◽  
Seyfi Yıldır ◽  
Gözde Türköz ◽  
Handan Çamdeviren Ankaralı ◽  
...  
2008 ◽  
Vol 26 (11) ◽  
pp. 1466-1470 ◽  
Author(s):  
Aspasia Tsezou ◽  
Tatsuya Furuichi ◽  
Maria Satra ◽  
Periklis Makrythanasis ◽  
Shiro Ikegawa ◽  
...  

2013 ◽  
Vol 33 (10) ◽  
pp. 2637-2645 ◽  
Author(s):  
Seyfi Yıldır ◽  
Melek Sezgin ◽  
İbrahim Ömer Barlas ◽  
Gözde Türköz ◽  
Handan Çamdeviren Ankaralı ◽  
...  

Author(s):  
Feifan Lu ◽  
Pei Liu ◽  
Qidong Zhang ◽  
Weiguo Wang ◽  
Wanshou Guo

Abstract Background Knee osteoarthritis is a joint disease which is characterized by degeneration of articular cartilage and subsequent subchondral bone changes. Polymorphisms of IL-17A/F gene were the recognized candidate genes associated with knee osteoarthritis risk although the results were conflicting. The aim of this study was to determine whether IL-17A(rs2275913) and IL-17F(rs763780) polymorphisms confer susceptibility to knee osteoarthritis. Method Literature search was performed in PubMed, Medline, Cochrane Library, Web of science, Embase, and Google Scholar (last search was updated on June 20, 2019), and assessing this association was performed by calculating odds ratios with 95% confidence intervals. Statistical heterogeneity was quantitatively evaluated by using the Q statistic with its p value and I2 statistic. Result Six case-control based studies were included involving IL-17A(rs2275913) (2134 cases and 2306 controls) and IL-17F(rs763780) (2134 cases and 2426 controls). The overall analysis suggested that the A allele of the rs2275913 polymorphism, and the C allele of the rs763780 polymorphism in the IL-17 gene may increase the risk of OA. However, subgroup analysis revealed that no association between IL-17A(rs2275913) gene and knee OA risk was found in Caucasian population. Conclusions This meta-analysis revealed that the IL-17A(rs2275913) gene polymorphisms may increase the risk of knee OA in Asians, and the IL-17F(rs763780) gene polymorphisms may increase the risk of knee OA both in Asians and Caucasians. However, because of the limitations of the present study, additional larger studies are needed to confirm our findings in the future.


2019 ◽  
Vol 39 (2) ◽  
Author(s):  
Gang Sun ◽  
Cheng-Lei Ba ◽  
Ren Gao ◽  
Wenqing Liu ◽  
Qiang Ji

Abstract Objective: To identify the association between the interleukin (IL) 6 (IL-6) rs1800795 (-174 G>C), IL-8 rs4073 (-251T>A), and matrix metalloproteinase-13 (MMP-13) rs2252070 (-77G>A) gene polymorphisms and knee osteoarthritis (KOA) susceptibility in the Chinese Han population. Methods: Genomic DNA was extracted from a total of 400 KOA patients and 400 healthy subjects. Sanger sequencing was performed to determine the genotypes of the IL-6 rs1800795 (-174 G/C), IL-8 rs4073 (-251A/T), and MMP-13 rs2252070 (-77A/G) loci. The mRNA expression levels of IL-6, IL-8, and MMP-13 in osteoblasts and the protein expression levels of IL-6, IL-8, and MMP-13 in the synovial fluids of KOA patients were analyzed. Results: The recessive model of IL-6 rs1800795 locus was found to be associated with KOA risk (adjusted odds ratio (OR) = 1.657, 95% confidence interval (CI) = 1.396–1.866, P<0.001). The IL-8 rs4073 locus dominant and recessive model showed no significant association with KOA risk (P>0.05). The dominant and recessive models of the MMP-13 rs2252070 locus showed higher risk for developing KOA (dominant model: adjusted OR = 1.271, 95%CI = 1.095–1.480, P=0.001; recessive model: adjusted OR = 1.361 95%CI = 1.151–1.569, P<0.001). The G>C mutation in IL-6 rs1800795 and the G>A mutation in MMP-13 rs2252070 were associated with significantly higher KOA disease severity. The G>C mutation in the IL-6 rs1800795 locus was associated with up-regulation of IL-6 expression. The G>A mutation in the MMP-13 rs2252070 locus was associated with up-regulation of MMP-13 expression. Conclusion: The IL-8 rs4073 (-251T>A) mutation was not associated with KOA susceptibility. The IL-6 rs1800795 (-174 G>C) and MMP-13 rs2252070 (-77G>A) mutations were associated with KOA susceptibility, increased disease severity, and up-regulation of IL-6 and MMP-13 expression levels.


Medicine ◽  
2019 ◽  
Vol 98 (13) ◽  
pp. e14933 ◽  
Author(s):  
Changcheng Wang ◽  
Li Luo ◽  
Fengde Tian ◽  
Ning An ◽  
Yao Zhang ◽  
...  

2009 ◽  
Vol 2 (1) ◽  
pp. 238 ◽  
Author(s):  
Koushik Chatterjee ◽  
Malin Engelmark ◽  
Ulf Gyllensten ◽  
Collet Dandara ◽  
Lize Merwe ◽  
...  

2021 ◽  
Vol 22 (2) ◽  
pp. 565-571
Author(s):  
Aziati Azwari Annuar ◽  
Ravindran Ankathil ◽  
Nazihah Mohd Yunus ◽  
Azlan Husin ◽  
Nur Shafawati Ab Rajab ◽  
...  

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