ArticleMolecular biology reports2011
Relationships between COL2A1 gene polymorphisms and knee osteoarthritis in Han Chinese women.
Article in Molecular biology reports, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.
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Who cites it
8 citing papers in PubMed, 1 synthesis or guideline pooled it, 14 citations in OpenAlex.
- C-Terminal Cross-Linked Telopeptides of Type II Collagen as Biomarker for Radiological Knee Osteoarthritis: A Meta-Analysis.Cartilage · 2020Pooled it
- Polygenetic Variants Related to Osteoarthritis Risk and Their Interactions with Energy, Protein, Fat, and Alcohol Intake in Adults in a Large Cohort.Diagnostics (Basel, Switzerland) · 2022Article
- Abnormal expression of miR-4784 in chondrocytes of osteoarthritis and associations with chondrocyte hyperplasia.Experimental and therapeutic medicine · 2018Article
- Association of COL1A1 rs1800012 polymorphism with musculoskeletal degenerative diseases: a meta-analysis.Oncotarget · 2017Article
- Occupational and genetic risk factors for osteoarthritis: a review.Work (Reading, Mass.) · 2015Review
- Gene expression profile analysis of human intervertebral disc degeneration.Genetics and molecular biology · 2013Article
- Highly accurate two-gene signature for gastric cancer.Medical oncology (Northwood, London, England) · 2013Article
- Osteoarthritic tissues modulate functional properties of sensory neurons associated with symptomatic OA pain.Molecular biology reports · 2011Article
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Authors and funding
3 authors at 2 institutions in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
To investigate the relationships between two COL2A1 single nucleotide polymorphisms (SNPs; T2088C and G4006A) and osteoarthritis (OA) in Han Chinese women. One hundred and twenty OA women and 120 control women were recruited. Genomic DNA was extracted from the whole blood. The COL2A1 polymorphisms T2088C and G4006A were analyzed by TaqMan assay. The levels of plasma N-propetide of type IIA collagen (PIIANP) and urinary C-telopeptide of type IIA collagen (CTX-II) were determined by ELISA. The level of plasma PIIANP significantly decreased in the OA group, compared with that in the control group (P<0.05), with 15.6±4.2 ng/ml (Mean±SD) in the OA group and 30.2±7.8 ng/ml in the control group. The level of urinary CTX-II significantly increased in the OA group, compared with that in the control group (P<0.05), with 201.4±10.2 ng/ml in the control group and 250.8±15.6 ng/ml in the OA group. There was no difference in the T2088C genotypes between the OA and control groups. The G4006A AA homozygous genotype significantly increased in the OA patients, when compared with that in the control women (P<0.05, χ2), with 24.2% (29/120) in the OA group and 10.0% (12/120) in the control group; The A allele accounted for 49.2% (118/240) in the OA group and 35.8% (86/240) in the control group. Among the G4006A genotypes, the plasma PIIANP level of the AA genotype (16.4±6.6 ng/ml) was significantly lower than those of the GG genotype (28.6±4.2 ng/ml) and GA genotype (21.5±8.0 ng/ml) while the urinary CTX-II level of the AA genotype (255.2±18.4 ng/ml) significantly increased, compared with those of the GG genotype (218.4±13.2 ng/ml) and GA genotype (221.2±15.6 ng/ml). The haplotype analysis shows that T-G was a protective factor for OA and that T-A was a risk factor. The AA genotype, A allele and T-A may increase the risk of OA in the Han Chinese women while T-G may protect these women from OA.
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