Associations between genetically predicted plasma protein levels and Alzheimer's disease risk: a study using genetic prediction models

被引:5
|
作者
Zhu, Jingjing [1 ]
Liu, Shuai [1 ]
Walker, Keenan A. [2 ]
Zhong, Hua [1 ]
Ghoneim, Dalia H. [1 ]
Zhang, Zichen [3 ]
Surendran, Praveen [4 ]
Fahle, Sarah [4 ]
Butterworth, Adam [4 ,5 ]
Alam, Md Ashad [6 ,7 ]
Deng, Hong-Wen [6 ]
Wu, Chong [3 ]
Wu, Lang [1 ]
机构
[1] Univ Hawaii Manoa, Univ Hawaii Canc Ctr, Populat Sci Pacific Program, Canc Epidemiol Div, Honolulu, HI 96813 USA
[2] NIA, Lab Behav Neurosci, Intramural Res Program, Baltimore, MD USA
[3] Univ Texas MD Anderson Canc Ctr, Dept Biostat, Houston, TX 77030 USA
[4] Univ Cambridge, Dept Publ Hlth & Primary Care, MRC BHF Cardiovasc Epidemiol Unit, Cambridge, England
[5] Univ Cambridge, Dept Publ Hlth & Primary Care, NIHR Blood & Transplant Res Unit Donor Hlth & Geno, Cambridge, England
[6] Tulane Univ, Tulane Ctr Biomed Informat & Genom, Deming Dept Med, Div Biomed Informat & Genom, 1440 Canal St, New Orleans, LA 70112 USA
[7] Ochsner Clin Fdn, Ctr Outcomes Res, New Orleans, LA 70121 USA
基金
美国国家卫生研究院; 英国医学研究理事会;
关键词
Genetic instrument; Protein biomarker; Alzheimer's disease; Risk; ROD FORMATION; NEURONS;
D O I
10.1186/s13195-023-01378-4
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
BackgroundSpecific peripheral proteins have been implicated to play an important role in the development of Alzheimer's disease (AD). However, the roles of additional novel protein biomarkers in AD etiology remains elusive. The availability of large-scale AD GWAS and plasma proteomic data provide the resources needed for the identification of causally relevant circulating proteins that may serve as risk factors for AD and potential therapeutic targets.MethodsWe established and validated genetic prediction models for protein levels in plasma as instruments to investigate the associations between genetically predicted protein levels and AD risk. We studied 71,880 (proxy) cases and 383,378 (proxy) controls of European descent.ResultsWe identified 69 proteins with genetically predicted concentrations showing associations with AD risk. The drugs almitrine and ciclopirox targeting ATP1A1 were suggested to have a potential for being repositioned for AD treatment.ConclusionsOur study provides additional insights into the underlying mechanisms of AD and potential therapeutic strategies.
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页数:16
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