Ovarian Cancer and Parkinson's Disease: A Bidirectional Mendelian Randomization Study

被引:2
|
作者
Guo, Jian-Zeng [1 ,2 ]
Xiao, Qian [1 ,2 ]
Wu, Lang [3 ]
Chen, Fa [4 ]
Yin, Jia-Li [1 ,5 ,6 ]
Qin, Xue [2 ]
Gong, Ting-Ting [2 ]
Wu, Qi-Jun [1 ,2 ,5 ,6 ]
机构
[1] China Med Univ, Shengjing Hosp, Dept Clin Epidemiol, Shenyang 110004, Peoples R China
[2] China Med Univ, Shengjing Hosp, Dept Obstet & Gynecol, Shenyang 110004, Peoples R China
[3] Univ Hawaii Manoa, Univ Hawaii, Populat Sci Pacific Program, Canc Epidemiol Div,Canc Ctr, Honolulu, HI 96813 USA
[4] Fujian Med Univ, Sch Publ Hlth, Dept Epidemiol & Hlth Stat, Fujian Prov Key Lab Environm Factors & Canc, Fuzhou 350122, Peoples R China
[5] China Med Univ, Shengjing Hosp, Clin Res Ctr, Shenyang 110004, Peoples R China
[6] China Med Univ, Shengjing Hosp, Key Lab Precis Med Res Major Chron Dis, Shenyang 110004, Peoples R China
关键词
genetic association; histotype; mendelian randomization; ovarian cancer; Parkinson's disease; INFLAMMATION; RISK;
D O I
10.3390/jcm12082961
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
(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.
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页数:9
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