Your browser doesn't support javascript.
loading
Ovarian Cancer and Parkinson's Disease: A Bidirectional Mendelian Randomization Study.
Guo, Jian-Zeng; Xiao, Qian; Wu, Lang; Chen, Fa; Yin, Jia-Li; Qin, Xue; Gong, Ting-Ting; Wu, Qi-Jun.
Afiliación
  • Guo JZ; Department of Clinical Epidemiology, Shengjing Hospital of China Medical University, Shenyang 110004, China.
  • Xiao Q; Department of Obstetrics and Gynecology, Shengjing Hospital of China Medical University, Shenyang 110004, China.
  • Wu L; Department of Clinical Epidemiology, Shengjing Hospital of China Medical University, Shenyang 110004, China.
  • Chen F; Department of Obstetrics and Gynecology, Shengjing Hospital of China Medical University, Shenyang 110004, China.
  • Yin JL; Cancer Epidemiology Division, Population Sciences in the Pacific Program, University of Hawaii Cancer Center, University of Hawaii at Manoa, Honolulu, HI 96813, USA.
  • Qin X; Fujian Provincial Key Laboratory of Environment Factors and Cancer, Department of Epidemiology and Health Statistics, School of Public Health, Fujian Medical University, Fuzhou 350122, China.
  • Gong TT; Department of Clinical Epidemiology, Shengjing Hospital of China Medical University, Shenyang 110004, China.
  • Wu QJ; Clinical Research Center, Shengjing Hospital of China Medical University, Shenyang 110004, China.
J Clin Med ; 12(8)2023 Apr 19.
Article en En | MEDLINE | ID: mdl-37109305
ABSTRACT
(1)

Background:

Ovarian cancer (OC) and Parkinson's disease (PD) represent a huge public health burden. The relationship of these two diseases is suggested in the literature while not fully understood. To better understand this relationship, we conducted a bidirectional Mendelian ran-domization analysis using genetic markers as a proxy. (2)

Methods:

Utilizing single nucleotide polymorphisms associated with PD risk, we assessed the association between genetically predicted PD and OC risk, overall and by histotypes, using summary statistics from previously conducted genome-wide association studies of OC within the Ovarian Cancer Association Consortium. Similarly, we assessed the association between genetically predicted OC and PD risk. The inverse variance weighted method was used as the main method to estimate odds ratios (OR) and 95% confidence intervals (CI) for the associations of interest. (3)

Results:

There was no significant association between genetically predicted PD and OC risk OR = 0.95 (95% CI 0.88-1.03), or between genetically predicted OC and PD risk OR = 0.80 (95% CI 0.61-1.06). On the other hand, when examined by histotypes, a suggestive inverse association was observed between genetically predicted high grade serous OC and PD risk OR = 0.91 (95% CI 0.84-0.99). (4)

Conclusions:

Overall, our study did not observe a strong genetic association between PD and OC, but the observed potential association between high grade serous OC and reduced PD risk warrants further investigation.
Palabras clave

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Clinical_trials / Prognostic_studies Idioma: En Revista: J Clin Med Año: 2023 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Clinical_trials / Prognostic_studies Idioma: En Revista: J Clin Med Año: 2023 Tipo del documento: Article País de afiliación: China
...