Ryan Tatton, Stephen O'Neill, Deondre Jordan, Lisa E Vaughan, John C Lieske, Mira T Keddis
{"title":"Kidney Stone Events and ESKD Incidence in Patients with Enteric Hyperoxaluria from Diverse Enteric Etiologies.","authors":"Ryan Tatton, Stephen O'Neill, Deondre Jordan, Lisa E Vaughan, John C Lieske, Mira T Keddis","doi":"10.34067/KID.0000000908","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Enteric Hyperoxaluria (EH) is a risk factor for calcium oxalate nephrolithiasis and kidney disease. The study compares patient characteristics and urine metabolic profiles at the time of EH diagnosis and kidney stones and end stage kidney disease (ESKD) events during follow-up in a cohort with diverse causes of EH.</p><p><strong>Methods: </strong>Adult patients with newly documented elevated urinary oxalate excretion (UOX) >40 mg/24hr between 1/1/2010 to 10/31/2023 and a known enteric diagnosis including inflammatory bowel disease, Exocrine Pancreatic Insufficiency (EPI), Celiac disease, Structural Intestinal Malabsorption (SIM), or Malabsorptive Bariatric surgery (Bariatric) were identified. Event rates and cumulative incidence of kidney stones and ESKD were assessed.</p><p><strong>Results: </strong>Among 814 identified patients, the most common enteric etiology was Bariatric (n=524, 64%). Patients with ulcerative colitis had the highest prevalence of kidney stones at EH diagnosis (93.6%) compared to other enteric etiologies (p=0.002). Patients with SIM had the highest urinary oxalate, lower urinary citrate, and volume, compared to other enteric etiologies (p<0.05). Calcium oxalate supersaturation was similar among the enteric groups (p=0.67). Median stone event rate for the overall cohort was 0.70 stone events/year during a mean (SD) follow-up of 5.0 (3.9) years. The SIM and EPI groups experienced the highest stone events (median (IQR) 1.24 (0.28, 2.40) and 1.20 (0.41, 1.99) events/year, respectively) while the Bariatric group had the lowest event rates (median (IQR) 0.45 (0.00, 1.66 events/year)) (p<0.001). The SIM group had the highest ESKD incidence (17.8% 5 years post-diagnosis; log-rank test p<0.001).</p><p><strong>Conclusions: </strong>We describe a large EH cohort from diverse enteric etiologies. Significant heterogeneity exists in patient characteristics, urine metabolic risk factors and adverse kidney outcomes. Patients with SIM and EPI experienced the highest kidney stone events and patients with SIM had the highest ESKD incidence. This study highlights the urgent need for more granular information regarding the natural history and risk factors for kidney complications for EH patients to support interventional trials to improve outcomes.</p>","PeriodicalId":17882,"journal":{"name":"Kidney360","volume":" ","pages":""},"PeriodicalIF":3.0000,"publicationDate":"2025-08-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Kidney360","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.34067/KID.0000000908","RegionNum":0,"RegionCategory":null,"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: Enteric Hyperoxaluria (EH) is a risk factor for calcium oxalate nephrolithiasis and kidney disease. The study compares patient characteristics and urine metabolic profiles at the time of EH diagnosis and kidney stones and end stage kidney disease (ESKD) events during follow-up in a cohort with diverse causes of EH.
Methods: Adult patients with newly documented elevated urinary oxalate excretion (UOX) >40 mg/24hr between 1/1/2010 to 10/31/2023 and a known enteric diagnosis including inflammatory bowel disease, Exocrine Pancreatic Insufficiency (EPI), Celiac disease, Structural Intestinal Malabsorption (SIM), or Malabsorptive Bariatric surgery (Bariatric) were identified. Event rates and cumulative incidence of kidney stones and ESKD were assessed.
Results: Among 814 identified patients, the most common enteric etiology was Bariatric (n=524, 64%). Patients with ulcerative colitis had the highest prevalence of kidney stones at EH diagnosis (93.6%) compared to other enteric etiologies (p=0.002). Patients with SIM had the highest urinary oxalate, lower urinary citrate, and volume, compared to other enteric etiologies (p<0.05). Calcium oxalate supersaturation was similar among the enteric groups (p=0.67). Median stone event rate for the overall cohort was 0.70 stone events/year during a mean (SD) follow-up of 5.0 (3.9) years. The SIM and EPI groups experienced the highest stone events (median (IQR) 1.24 (0.28, 2.40) and 1.20 (0.41, 1.99) events/year, respectively) while the Bariatric group had the lowest event rates (median (IQR) 0.45 (0.00, 1.66 events/year)) (p<0.001). The SIM group had the highest ESKD incidence (17.8% 5 years post-diagnosis; log-rank test p<0.001).
Conclusions: We describe a large EH cohort from diverse enteric etiologies. Significant heterogeneity exists in patient characteristics, urine metabolic risk factors and adverse kidney outcomes. Patients with SIM and EPI experienced the highest kidney stone events and patients with SIM had the highest ESKD incidence. This study highlights the urgent need for more granular information regarding the natural history and risk factors for kidney complications for EH patients to support interventional trials to improve outcomes.