Hsiao-Mei Tsao,Yu-Hsuan Joni Shao,Yi-Cheng Chang,Yu-Hsiang Chou,Vin-Cent Wu,Shuei-Liong Lin,Yung-Ming Chen,Tai-Shuan Lai
{"title":"揭示甲状腺和肾脏功能之间的因果关系:一个多变量孟德尔随机化。","authors":"Hsiao-Mei Tsao,Yu-Hsuan Joni Shao,Yi-Cheng Chang,Yu-Hsiang Chou,Vin-Cent Wu,Shuei-Liong Lin,Yung-Ming Chen,Tai-Shuan Lai","doi":"10.2215/cjn.0000000722","DOIUrl":null,"url":null,"abstract":"BACKGROUND\r\nRecent studies suggest an association between thyroid dysfunction and kidney function, but the causal relationship remains uncertain. The complex interactions between thyroid-stimulating hormone (TSH), free thyroxine (fT4), and thyroid peroxidase antibodies (TPOAb) complicate the assessment of this link. This study employed multivariable Mendelian randomization (MVMR) to elucidate the causal relationship between thyroid dysfunction and kidney function in East Asian and European populations.\r\n\r\nMETHODS\r\nWe conducted a cross-sectional study and MVMR analysis using data from 17,733 participants in the Taiwan Biobank. Thyroid function was assessed by measuring TSH, fT4 and TPOAb levels, with hypothyroidism classified as subclinical or overt. The primary outcome was creatinine-based estimated glomerular filtration rate (eGFR), calculated using the Chronic Kidney Disease-EPIdemiology Collaboration equation. Observational analyses were adjusted for age, sex, body mass index, and metabolic and cardiovascular factors. MVMR analyses used genetic variants associated with TSH, fT4, and TPOAb levels to assess their causal effects on eGFR. Data from the ThyroidOmics and CKDGen Consortium were used to replicate findings in European populations.\r\n\r\nRESULTS\r\nBoth TSH and fT4 levels were inversely associated with eGFR, and hypothyroidism was correlated with lower eGFR. Conversely, TPOAb was positively associated with eGFR. Mendelian randomization analyses, using 26 genetic variants for TSH, four for fT4, and eight for TPOAb confirmed a causal relationship between TSH and eGFR. Significant causal effects of TSH were observed across various MVMR methods (P values from <0.001 to 0.01), whereas fT4 and TPOAb showed no significant causal effects (both P >0.05). These findings were consistent in European populations.\r\n\r\nCONCLUSIONS\r\nThe study found that elevated TSH levels are causally associated with reduced kidney function, highlighting the potential importance of thyroid function in kidney health. These findings suggest that thyroid dysfunction should be considered in managing patients with chronic kidney disease.","PeriodicalId":50681,"journal":{"name":"Clinical Journal of the American Society of Nephrology","volume":"43 1","pages":""},"PeriodicalIF":8.5000,"publicationDate":"2025-04-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Unveiling the Causal Relationship Between Thyroid and Kidney Function: A Multivariable Mendelian Randomization.\",\"authors\":\"Hsiao-Mei Tsao,Yu-Hsuan Joni Shao,Yi-Cheng Chang,Yu-Hsiang Chou,Vin-Cent Wu,Shuei-Liong Lin,Yung-Ming Chen,Tai-Shuan Lai\",\"doi\":\"10.2215/cjn.0000000722\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"BACKGROUND\\r\\nRecent studies suggest an association between thyroid dysfunction and kidney function, but the causal relationship remains uncertain. The complex interactions between thyroid-stimulating hormone (TSH), free thyroxine (fT4), and thyroid peroxidase antibodies (TPOAb) complicate the assessment of this link. This study employed multivariable Mendelian randomization (MVMR) to elucidate the causal relationship between thyroid dysfunction and kidney function in East Asian and European populations.\\r\\n\\r\\nMETHODS\\r\\nWe conducted a cross-sectional study and MVMR analysis using data from 17,733 participants in the Taiwan Biobank. Thyroid function was assessed by measuring TSH, fT4 and TPOAb levels, with hypothyroidism classified as subclinical or overt. The primary outcome was creatinine-based estimated glomerular filtration rate (eGFR), calculated using the Chronic Kidney Disease-EPIdemiology Collaboration equation. Observational analyses were adjusted for age, sex, body mass index, and metabolic and cardiovascular factors. MVMR analyses used genetic variants associated with TSH, fT4, and TPOAb levels to assess their causal effects on eGFR. Data from the ThyroidOmics and CKDGen Consortium were used to replicate findings in European populations.\\r\\n\\r\\nRESULTS\\r\\nBoth TSH and fT4 levels were inversely associated with eGFR, and hypothyroidism was correlated with lower eGFR. Conversely, TPOAb was positively associated with eGFR. Mendelian randomization analyses, using 26 genetic variants for TSH, four for fT4, and eight for TPOAb confirmed a causal relationship between TSH and eGFR. Significant causal effects of TSH were observed across various MVMR methods (P values from <0.001 to 0.01), whereas fT4 and TPOAb showed no significant causal effects (both P >0.05). These findings were consistent in European populations.\\r\\n\\r\\nCONCLUSIONS\\r\\nThe study found that elevated TSH levels are causally associated with reduced kidney function, highlighting the potential importance of thyroid function in kidney health. 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Unveiling the Causal Relationship Between Thyroid and Kidney Function: A Multivariable Mendelian Randomization.
BACKGROUND
Recent studies suggest an association between thyroid dysfunction and kidney function, but the causal relationship remains uncertain. The complex interactions between thyroid-stimulating hormone (TSH), free thyroxine (fT4), and thyroid peroxidase antibodies (TPOAb) complicate the assessment of this link. This study employed multivariable Mendelian randomization (MVMR) to elucidate the causal relationship between thyroid dysfunction and kidney function in East Asian and European populations.
METHODS
We conducted a cross-sectional study and MVMR analysis using data from 17,733 participants in the Taiwan Biobank. Thyroid function was assessed by measuring TSH, fT4 and TPOAb levels, with hypothyroidism classified as subclinical or overt. The primary outcome was creatinine-based estimated glomerular filtration rate (eGFR), calculated using the Chronic Kidney Disease-EPIdemiology Collaboration equation. Observational analyses were adjusted for age, sex, body mass index, and metabolic and cardiovascular factors. MVMR analyses used genetic variants associated with TSH, fT4, and TPOAb levels to assess their causal effects on eGFR. Data from the ThyroidOmics and CKDGen Consortium were used to replicate findings in European populations.
RESULTS
Both TSH and fT4 levels were inversely associated with eGFR, and hypothyroidism was correlated with lower eGFR. Conversely, TPOAb was positively associated with eGFR. Mendelian randomization analyses, using 26 genetic variants for TSH, four for fT4, and eight for TPOAb confirmed a causal relationship between TSH and eGFR. Significant causal effects of TSH were observed across various MVMR methods (P values from <0.001 to 0.01), whereas fT4 and TPOAb showed no significant causal effects (both P >0.05). These findings were consistent in European populations.
CONCLUSIONS
The study found that elevated TSH levels are causally associated with reduced kidney function, highlighting the potential importance of thyroid function in kidney health. These findings suggest that thyroid dysfunction should be considered in managing patients with chronic kidney disease.
期刊介绍:
The Clinical Journal of the American Society of Nephrology strives to establish itself as the foremost authority in communicating and influencing advances in clinical nephrology by (1) swiftly and effectively disseminating pivotal developments in clinical and translational research in nephrology, encompassing innovations in research methods and care delivery; (2) providing context for these advances in relation to future research directions and patient care; and (3) becoming a key voice on issues with potential implications for the clinical practice of nephrology, particularly within the United States. Original manuscript topics cover a range of areas, including Acid/Base and Electrolyte Disorders, Acute Kidney Injury and ICU Nephrology, Chronic Kidney Disease, Clinical Nephrology, Cystic Kidney Disease, Diabetes and the Kidney, Genetics, Geriatric and Palliative Nephrology, Glomerular and Tubulointerstitial Diseases, Hypertension, Maintenance Dialysis, Mineral Metabolism, Nephrolithiasis, and Transplantation.