Lauren Bernard, Jiaqi Yang, Jingsha Chen, Valerie K Sullivan, Bing Yu, Eugene P Rhee, Paul A Welling, Casey M Rebholz
{"title":"Serum Metabolomic Markers of Dietary Potassium and Risk of Chronic Kidney Disease.","authors":"Lauren Bernard, Jiaqi Yang, Jingsha Chen, Valerie K Sullivan, Bing Yu, Eugene P Rhee, Paul A Welling, Casey M Rebholz","doi":"10.2215/CJN.0000000675","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Discovering metabolomic markers of dietary potassium may help improve dietary assessment of potassium and trace the impact of dietary potassium on chronic kidney disease (CKD) development.</p><p><strong>Methods: </strong>We included adults from the Atherosclerosis Risk in Communities (ARIC) study without CKD at visit 1 (N = 3,812). Cross-sectional associations between dietary potassium and serum metabolites were assessed using multivariable linear regression models. Cox regression models estimated hazard ratios for potassium-related metabolites and incident CKD. Incident CKD was defined as estimated glomerular filtration rate (<60 mL/min/1.73 m2 and ≥25% decline), CKD-related hospitalization or death, or kidney replacement therapy identified via United States Renal Data System registry from visit 1 (1987-1989) through December 31, 2020.</p><p><strong>Results: </strong>There were 33 significant associations between dietary potassium and serum metabolites, including pyridoxate, N-methylproline, stachydrine, pantothenate, and scyllo-inositol. During more than two decades of follow-up (median: 23 years, 25th-75th percentile: 14-30), 1,616 (42%) of participants developed incident CKD. Ten of the 33 potassium-related metabolites were significantly associated with incident CKD. Metabolites involved in phenylalanine and tyrosine metabolism, 3-(4-hydroxyphenyl)lactate and 3-phenylpropionate, were significantly associated with dietary potassium and CKD. Additionally, glycerate, involved in glucose metabolism, was positively associated with dietary potassium (β=0.09, p=4.01 x 10-17) and inversely associated with CKD (HR 0.77, 95% CI: 0.69-0.85, p=8.57 x 10-7). There was a significant trend for CKD risk across quartiles of 3-(4-hydroxyphenyl)lactate, 3-phenylpropionate, and glycerate.</p><p><strong>Conclusions: </strong>Dietary potassium was associated with 33 serum metabolites. 3-(4-hydroxyphenyl)lactate 3-phenylpropionate, and glycerate are candidate markers of dietary potassium's impact on chronic kidney disease.</p>","PeriodicalId":50681,"journal":{"name":"Clinical Journal of the American Society of Nephrology","volume":" ","pages":""},"PeriodicalIF":8.5000,"publicationDate":"2025-03-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Clinical Journal of the American Society of Nephrology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.2215/CJN.0000000675","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"UROLOGY & NEPHROLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Background: Discovering metabolomic markers of dietary potassium may help improve dietary assessment of potassium and trace the impact of dietary potassium on chronic kidney disease (CKD) development.
Methods: We included adults from the Atherosclerosis Risk in Communities (ARIC) study without CKD at visit 1 (N = 3,812). Cross-sectional associations between dietary potassium and serum metabolites were assessed using multivariable linear regression models. Cox regression models estimated hazard ratios for potassium-related metabolites and incident CKD. Incident CKD was defined as estimated glomerular filtration rate (<60 mL/min/1.73 m2 and ≥25% decline), CKD-related hospitalization or death, or kidney replacement therapy identified via United States Renal Data System registry from visit 1 (1987-1989) through December 31, 2020.
Results: There were 33 significant associations between dietary potassium and serum metabolites, including pyridoxate, N-methylproline, stachydrine, pantothenate, and scyllo-inositol. During more than two decades of follow-up (median: 23 years, 25th-75th percentile: 14-30), 1,616 (42%) of participants developed incident CKD. Ten of the 33 potassium-related metabolites were significantly associated with incident CKD. Metabolites involved in phenylalanine and tyrosine metabolism, 3-(4-hydroxyphenyl)lactate and 3-phenylpropionate, were significantly associated with dietary potassium and CKD. Additionally, glycerate, involved in glucose metabolism, was positively associated with dietary potassium (β=0.09, p=4.01 x 10-17) and inversely associated with CKD (HR 0.77, 95% CI: 0.69-0.85, p=8.57 x 10-7). There was a significant trend for CKD risk across quartiles of 3-(4-hydroxyphenyl)lactate, 3-phenylpropionate, and glycerate.
Conclusions: Dietary potassium was associated with 33 serum metabolites. 3-(4-hydroxyphenyl)lactate 3-phenylpropionate, and glycerate are candidate markers of dietary potassium's impact on 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.