Testing relationship between tea intake and the risk of rheumatoid arthritis and systemic lupus erythematosus: a Mendelian randomization study

被引:3
作者
Lu, Rong-Bin [1 ]
Huang, Jian [2 ]
机构
[1] Guangxi Med Univ, Dept Orthoped Trauma & Hand Surg, Affiliated Hosp 1, Nanning 530021, Peoples R China
[2] Guangxi Med Univ, Clin Lab Ctr, Affiliated Hosp 1, Nanning 530021, Peoples R China
关键词
Mendelian randomization; Rheumatoid arthritis; Systemic lupus erythematosus; Tea intake; CONSUMPTION; COFFEE; EGCG; INFLAMMATION; INSTRUMENTS; EXTRACT;
D O I
10.1186/s42358-023-00290-7
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BackgroundWe performed Mendelian randomization (MR) to assess the causal effect of tea intake on rheumatoid arthritis (RA) and systemic lupus erythematosus (SLE).MethodsGenetic instruments for tea intake were obtained from a large genome-wide association study (GWAS) dataset of the UK Biobank. Genetic association estimates for RA (6236 cases and 147,221 controls) and SLE (538 cases and 213,145 controls) were obtained from the FinnGen study through the IEU GWAS database.ResultsMR analyses using the inverse-variance weighted method showed that tea intake was not associated with risk of RA [odds ratio (OR) per standard deviation increment in genetically predicted tea intake = 0.997, 95% confidence interval (CI) 0.658-1.511] and SLE (OR per standard deviation increment in genetically predicted tea intake = 0.961, 95% CI 0.299-3.092). Weighted median, weighted mode, MR-Egger, leave-one-out and multivariable MR controlling for several confounding factors including current tobacco smoking, coffee intake, and alcoholic drinks per week yielded completely consistent results. No evidence of heterogeneity and pleiotropy was found.ConclusionOur MR study did not suggest a causal effect of genetically predicted tea intake on RA and SLE.
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页数:8
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共 43 条
[1]   Caffeine, Coffee, Tea and Risk of Rheumatoid Arthritis: Systematic Review and Dose-Response Meta-analysis of Prospective Cohort Studies [J].
Asoudeh, Farzaneh ;
Dashti, Fatemeh ;
Jayedi, Ahmad ;
Hemmati, Amirhossein ;
Fadel, Abdulmannan ;
Mohammadi, Hamed .
FRONTIERS IN NUTRITION, 2022, 9
[2]  
Bae SC, 2019, Z RHEUMATOL, V78, P791, DOI 10.1007/s00393-018-0537-z
[3]   Coffee consumption and the risk of rheumatoid arthritis and systemic lupus erythematosus: a Mendelian randomization study [J].
Bae, Sang-Cheol ;
Lee, Young Ho .
CLINICAL RHEUMATOLOGY, 2018, 37 (10) :2875-2879
[4]   Micronutrients: Essential Treatment for Inflammatory Arthritis? [J].
Banuls-Mirete, Marina ;
Ogdie, Alexis ;
Guma, Monica .
CURRENT RHEUMATOLOGY REPORTS, 2020, 22 (12)
[5]   Global epidemiology of systemic lupus erythematosus [J].
Barber, Megan R. W. ;
Drenkard, Cristina ;
Falasinnu, Titilola ;
Hoi, Alberta ;
Mak, Anselm ;
Kow, Nien Yee ;
Svenungsson, Elisabet ;
Peterson, Jonna ;
Clarke, Ann E. ;
Ramsey-Goldman, Rosalind .
NATURE REVIEWS RHEUMATOLOGY, 2021, 17 (09) :515-532
[6]   A framework for the investigation of pleiotropy in two-sample summary data Mendelian randomization [J].
Bowden, Jack ;
Del Greco, Fabiola M. ;
Minelli, Cosetta ;
Smith, George Davey ;
Sheehan, Nuala ;
Thompson, John .
STATISTICS IN MEDICINE, 2017, 36 (11) :1783-1802
[7]   Consistent Estimation in Mendelian Randomization with Some Invalid Instruments Using a Weighted Median Estimator [J].
Bowden, Jack ;
Smith, George Davey ;
Haycock, Philip C. ;
Burgess, Stephen .
GENETIC EPIDEMIOLOGY, 2016, 40 (04) :304-314
[8]   Sensitivity Analyses for Robust Causal Inference from Mendelian Randomization Analyses with Multiple Genetic Variants [J].
Burgess, Stephen ;
Bowden, Jack ;
Fall, Tove ;
Ingelsson, Erik ;
Thompson, Simon G. .
EPIDEMIOLOGY, 2017, 28 (01) :30-42
[9]   Multivariable Mendelian Randomization: The Use of Pleiotropic Genetic Variants to Estimate Causal Effects [J].
Burgess, Stephen ;
Thompson, Simon G. .
AMERICAN JOURNAL OF EPIDEMIOLOGY, 2015, 181 (04) :251-260
[10]   Avoiding bias from weak instruments in Mendelian randomization studies [J].
Burgess, Stephen ;
Thompson, Simon G. .
INTERNATIONAL JOURNAL OF EPIDEMIOLOGY, 2011, 40 (03) :755-764