Evidence map›Paper›PMID 41284113›Full record

ArticleClinical and experimental nephrology2026

Causal relationships of Janus kinase 2 with chronic kidney diseases: a two-sample Mendelian randomisation study.

Yanjun Wang, Yanling Ding, Jiatong Zhang, Tana Wuren

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Article in Clinical and experimental nephrology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 authors.

Yanjun WangDepartment of Geriatrics, Affiliated Hospital of Qinghai University, Xining, 810001, Qinghai, China.
Yanling DingDepartment of Nephrology, Affiliated Hospital of Qinghai University, Xining, 810001, Qinghai, China.
Jiatong ZhangSchool of Clinical Medicine, Queen Mary College, Nanchang University, Nanchang, China.
Tana WurenResearch Center for High Altitude Medicine, Qinghai University, Xining, 810001, Qinghai, China. tana.wuren@qhu.edu.cn.

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6 · The paper itself

Abstract

backgroundThe role of Janus kinase (JAK) 2 in chronic kidney disease (CKD) remains unreported. This Mendelian randomisation (MR) study investigates the causal associations of JAK2 with CKD and provides references for the identification of possible therapeutic targets and the prevention of renal dysfunction.

methodsSummary data for JAK2 and various CKD endpoints are extracted from genome-wide association study findings provided by the MRC Integrative Epidemiology Unit and FinnGen. The causal relationships are assessed using inverse variance weighted estimates, weighted median and MR-Egger regression. To ensure rigour, reverse MR, radial MR and leave-one-out approaches are employed for sensitivity analyses, with Cochran's Q used to assess heterogeneity.

resultsInverse variance weighted estimates indicate potential two-way causal associations between JAK2 and membranous nephropathy (MN) (odds ratio [OR] = 1.138, 95% confidence interval [CI]: 1.073-1.206; reverse causal association: OR = 1.040, 95% CI: 1.002-1.079). Sensitivity analyses demonstrate that these relationships are relatively robust. An underlying causal relationship between JAK2 and estimated glomerular filtration rate is identified (OR = 0.996, 95%CI 0.993-1.000); however, this becomes non-significant after the radial MR test (P > 0.05). In addition, polycystic kidney disease exhibits a potential causal relationship with JAK2 (OR = 1.066, 95%CI 1.009-1.127).

conclusionsElevated relative expression of JAK2 may represent a potential risk factor for the occurrence of MN. Conversely, patients with MN may exhibit high relative expression of JAK2. These two-way causal associations may inform future efforts aimed at the prevention of CKD and the identification of possible therapeutic targets.

Indexed as

Janus Kinase 2Renal Insufficiency, ChronicGenetic Predisposition to DiseaseGenome-Wide Association StudyGlomerular Filtration RateHumansMendelian Randomization AnalysisPolymorphism, Single NucleotideRisk FactorsJAK2 protein, humanJanus Kinase 2Causal associationChronic kidney diseasesEstimated glomerular filtration rateJanus kinase 2Mendelian randomisation

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.