Parisa Mortaji , Xuan Cai , Ester Oh , Rebecca Frazier , Anand Srivastava , Michael Fischer , Ana Ricardo , Jiang He , Katherine Mills , Katherine Wolfrum , Amanda Anderson , Harold I. Feldman , Makoto Miyazaki , Michel Chonchol , Manjula Kurella Tamura , Kristen Nowak , Tamara Isakova , Anna Jovanovich
{"title":"Deoxycholic Acid and Cognitive Impairment and Decline in the Chronic Renal Insufficiency Cohort (CRIC)","authors":"Parisa Mortaji , Xuan Cai , Ester Oh , Rebecca Frazier , Anand Srivastava , Michael Fischer , Ana Ricardo , Jiang He , Katherine Mills , Katherine Wolfrum , Amanda Anderson , Harold I. Feldman , Makoto Miyazaki , Michel Chonchol , Manjula Kurella Tamura , Kristen Nowak , Tamara Isakova , Anna Jovanovich","doi":"10.1016/j.xkme.2025.101018","DOIUrl":null,"url":null,"abstract":"<div><h3>Rationale & Objective</h3><div>Cognitive impairment is common in chronic kidney disease (CKD). The secondary bile acid, deoxycholic acid (DCA), is associated with cognitive impairment and Alzheimer’s dementia among older adults without CKD. Whether DCA is associated with cognitive impairment and decline in CKD is unknown.</div></div><div><h3>Study Design</h3><div>Cross-sectional and longitudinal multivariable-adjusted regression analyses.</div></div><div><h3>Setting & Participants</h3><div>2,836 CRIC Study participants; 699 CRIC Cognitive (COG) Study participants.</div></div><div><h3>Exposure</h3><div>Fasting serum DCA levels measured at visit 5 (ie, baseline).</div></div><div><h3>Outcomes</h3><div>Modified Mini-Mental State Examination (3MS) in the main CRIC cohort and domain-specific cognitive tests in the CRIC COG cohort: Trail Making Test Parts A and B, Category Fluency, Buschke Selective Reminding, and Boston Naming. Cognitive impairment was defined as test score<!--> <!-->>1 standard deviation worse than the mean test score.</div></div><div><h3>Results</h3><div>Mean age 59<!--> <!-->±<!--> <!-->10 years, 45% female, and 39% Black. In the overall cohort, in cross-sectional analyses, there was no association between DCA and cognitive impairment by 3MS in after adjustment for demographics and clinical factors (prevalence ratio doubling DCA, 1.00; 95% CI, 0.95-1.06; n<!--> <!-->=<!--> <!-->2,836). In longitudinal analyses, DCA was associated with decline (mean annual percent change in 3MS per doubling DCA, −0.13; 95% CI, −0.28 to<!--> <!-->−0.02) but not with incident impairment (n<!--> <!-->=<!--> <!-->2,836; follow-up of 8.6<!--> <!-->±<!--> <!-->3.9 years). Among CRIC COG Study participants, in cross-sectional analyses, DCA was associated with cognitive impairment based on Category Fluency (prevalence ratio per doubling DCA, 1.14; 95% CI, 1.02-1.27) but not with other specific-domain cognitive tests (n<!--> <!-->=<!--> <!-->698-699). In CRIC COG longitudinal analyses, DCA was not associated with decline or incident cognitive impairment (n<!--> <!-->=<!--> <!-->538-574).</div></div><div><h3>Limitations</h3><div>No adjustment for inflammation, no stool DCA, 3MS may lack specificity.</div></div><div><h3>Conclusion</h3><div>Among individuals with CKD stages 2-4, higher DCA levels were independently associated with prevalent cognitive impairment in Category Fluency. The association between DCA and progressive cognitive impairment assessed by 3MS was small and likely not clinically significant.</div></div><div><h3>Plain-Language Summary</h3><div>Cognitive impairment is common in chronic kidney disease (CKD). Deoxycholic acid (DCA) is a secondary bile acid that is associated with cognitive impairment in older adults without CKD, but its association with cognitive impairment and decline in patients with CKD is unknown. We examined whether DCA was associated with baseline or later cognitive impairment among 2,836 participants from a cohort of adults with CKD stages 2-4. Although higher DCA levels were associated with one measure of cognitive impairment at baseline, the association with progressive cognitive impairment was small and likely not clinically significant.</div></div>","PeriodicalId":17885,"journal":{"name":"Kidney Medicine","volume":"7 7","pages":"Article 101018"},"PeriodicalIF":3.2000,"publicationDate":"2025-04-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Kidney Medicine","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2590059525000548","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
Rationale & Objective
Cognitive impairment is common in chronic kidney disease (CKD). The secondary bile acid, deoxycholic acid (DCA), is associated with cognitive impairment and Alzheimer’s dementia among older adults without CKD. Whether DCA is associated with cognitive impairment and decline in CKD is unknown.
Study Design
Cross-sectional and longitudinal multivariable-adjusted regression analyses.
Setting & Participants
2,836 CRIC Study participants; 699 CRIC Cognitive (COG) Study participants.
Exposure
Fasting serum DCA levels measured at visit 5 (ie, baseline).
Outcomes
Modified Mini-Mental State Examination (3MS) in the main CRIC cohort and domain-specific cognitive tests in the CRIC COG cohort: Trail Making Test Parts A and B, Category Fluency, Buschke Selective Reminding, and Boston Naming. Cognitive impairment was defined as test score >1 standard deviation worse than the mean test score.
Results
Mean age 59 ± 10 years, 45% female, and 39% Black. In the overall cohort, in cross-sectional analyses, there was no association between DCA and cognitive impairment by 3MS in after adjustment for demographics and clinical factors (prevalence ratio doubling DCA, 1.00; 95% CI, 0.95-1.06; n = 2,836). In longitudinal analyses, DCA was associated with decline (mean annual percent change in 3MS per doubling DCA, −0.13; 95% CI, −0.28 to −0.02) but not with incident impairment (n = 2,836; follow-up of 8.6 ± 3.9 years). Among CRIC COG Study participants, in cross-sectional analyses, DCA was associated with cognitive impairment based on Category Fluency (prevalence ratio per doubling DCA, 1.14; 95% CI, 1.02-1.27) but not with other specific-domain cognitive tests (n = 698-699). In CRIC COG longitudinal analyses, DCA was not associated with decline or incident cognitive impairment (n = 538-574).
Limitations
No adjustment for inflammation, no stool DCA, 3MS may lack specificity.
Conclusion
Among individuals with CKD stages 2-4, higher DCA levels were independently associated with prevalent cognitive impairment in Category Fluency. The association between DCA and progressive cognitive impairment assessed by 3MS was small and likely not clinically significant.
Plain-Language Summary
Cognitive impairment is common in chronic kidney disease (CKD). Deoxycholic acid (DCA) is a secondary bile acid that is associated with cognitive impairment in older adults without CKD, but its association with cognitive impairment and decline in patients with CKD is unknown. We examined whether DCA was associated with baseline or later cognitive impairment among 2,836 participants from a cohort of adults with CKD stages 2-4. Although higher DCA levels were associated with one measure of cognitive impairment at baseline, the association with progressive cognitive impairment was small and likely not clinically significant.