Unraveling the genetic association between knee osteoarthritis and hallux deformities

Zhengtao Lv1, Mingchao Lin2,3, Jiaming Zhang4

  • 1Department of Orthopedics, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430030, People's Republic of China.

Insights

Knee osteoarthritis (KOA) genetically causes hallux valgus (HV) and hallux rigidus (HR). This genetic link between KOA and hallux deformities suggests targeted interventions for KOA patients.

Area of Science:

  • Genetics
  • Orthopedics
  • Epidemiology

Background:

  • Knee osteoarthritis (KOA), hallux valgus (HV), and hallux rigidus (HR) are prevalent lower extremity musculoskeletal conditions.
  • The causal relationship between KOA and hallux deformities remains unclear, necessitating investigation.

Purpose of the Study:

  • To elucidate the cause-and-effect relationship between knee osteoarthritis and the development of hallux valgus and hallux rigidus.
  • To establish genetic causality between KOA and hallux deformities using Mendelian randomization.

Main Methods:

  • Summary-level statistics from genome-wide association studies (GWAS) for KOA, HV, and HR were utilized.
  • Two-sample Mendelian randomization (MR) analyses were performed to assess causality.
  • Sensitivity analyses, multivariable MR (MVMR), and backward MR were conducted to ensure robustness and explore confounding factors.

Main Results:

  • Univariable MR indicated that KOA causally influences HR (OR=1.29) and HV (OR=1.43).
  • Backward MR analyses revealed no evidence that hallux deformities cause KOA.
  • MVMR confirmed the robust causal impact of KOA on HV and HR, even after adjusting for anthropometric characteristics like BMI and waist-to-hip ratio.

Conclusions:

  • This study establishes a genetic causality between knee osteoarthritis and an increased risk of hallux deformities (HV and HR).
  • Findings provide evidence for targeted interventions to reduce hallux deformity incidence in KOA patients.
  • Further research is recommended to validate these associations and explore broader clinical implications.
Abstract