Nusrat E Mozid, Imran Hossain Monju, Shakila Sharmin, Sanjana Binte Ahmed
{"title":"A pragmatic Three-Component Clinical Score for Cognitive Risk Stratification in Older Adults with Multimorbidity and Frailty.","authors":"Nusrat E Mozid, Imran Hossain Monju, Shakila Sharmin, Sanjana Binte Ahmed","doi":"10.1093/gerona/glag117","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Simple, scalable clinical tools are needed to identify older adults with prevalent cognitive impairment in low-resource settings, yet whether parsimonious approaches can match complex phenotyping methods remains unclear. This study developed a three-component clinical score and compared its discriminative performance with latent class analysis (LCA)-derived multimorbidity phenotypes.</p><p><strong>Methods: </strong>This cross-sectional study was conducted in two districts of Bangladesh included 504 community-dwelling adults aged ≥65 years with at least one chronic disease. Frailty was assessed using the Fried phenotype, and multimorbidity was self-reported and coded using ICD-10. An additive score (0-5 points) incorporating age ≥80 years, ≥3 chronic conditions, and frailty classified participants into low (0-1), moderate (2-3), or high (4-5) risk. Outcomes included global cognition and cognitive impairment (MMSE < 25).</p><p><strong>Results: </strong>The three-component score showed acceptable discrimination for cognitive impairment (AUC = 0.72) and explained 33% of MMSE variance. LCA-derived phenotypes demonstrated poor discrimination (AUC = 0.44; difference = 0.28, p < 0.001). A monotonic gradient was observed across risk categories, impairment prevalence increased across risk categories (59%, 83%, and 96%), corresponding to a 12.8-point MMSE difference across the score range. A frailty-augmented LCA (in which frailty was added to the original disease-only LCA) combined with age yielded a modestly higher AUC (0.764), though at substantially greater analytical complexity.</p><p><strong>Conclusions: </strong>A parsimonious clinical score combining age, multimorbidity, and frailty demonstrated acceptable cross-sectional discrimination for prevalent cognitive impairment and substantially outperformed disease-only multimorbidity phenotyping. Given the cross-sectional design, conclusions pertain to prevalence-based risk stratification rather than prediction of incident cognitive decline. Subject to prospective validation, this pragmatic tool may support case-finding and cognitive risk stratification in resource-limited settings.</p>","PeriodicalId":94243,"journal":{"name":"The journals of gerontology. Series A, Biological sciences and medical sciences","volume":" ","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2026-05-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"The journals of gerontology. Series A, Biological sciences and medical sciences","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1093/gerona/glag117","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Background: Simple, scalable clinical tools are needed to identify older adults with prevalent cognitive impairment in low-resource settings, yet whether parsimonious approaches can match complex phenotyping methods remains unclear. This study developed a three-component clinical score and compared its discriminative performance with latent class analysis (LCA)-derived multimorbidity phenotypes.
Methods: This cross-sectional study was conducted in two districts of Bangladesh included 504 community-dwelling adults aged ≥65 years with at least one chronic disease. Frailty was assessed using the Fried phenotype, and multimorbidity was self-reported and coded using ICD-10. An additive score (0-5 points) incorporating age ≥80 years, ≥3 chronic conditions, and frailty classified participants into low (0-1), moderate (2-3), or high (4-5) risk. Outcomes included global cognition and cognitive impairment (MMSE < 25).
Results: The three-component score showed acceptable discrimination for cognitive impairment (AUC = 0.72) and explained 33% of MMSE variance. LCA-derived phenotypes demonstrated poor discrimination (AUC = 0.44; difference = 0.28, p < 0.001). A monotonic gradient was observed across risk categories, impairment prevalence increased across risk categories (59%, 83%, and 96%), corresponding to a 12.8-point MMSE difference across the score range. A frailty-augmented LCA (in which frailty was added to the original disease-only LCA) combined with age yielded a modestly higher AUC (0.764), though at substantially greater analytical complexity.
Conclusions: A parsimonious clinical score combining age, multimorbidity, and frailty demonstrated acceptable cross-sectional discrimination for prevalent cognitive impairment and substantially outperformed disease-only multimorbidity phenotyping. Given the cross-sectional design, conclusions pertain to prevalence-based risk stratification rather than prediction of incident cognitive decline. Subject to prospective validation, this pragmatic tool may support case-finding and cognitive risk stratification in resource-limited settings.