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Assessment of Vascular Function in Patients With Chronic Kidney Disease
Published on: June 16, 2014
Cognitive Impairment Predicts Adverse Outcomes in CKD
Hélène Levassort1,2, Yousra Hassan2, Julie Boucquemont2
1Geriatric Department, University Medical Department 1, Assistance Publique - Hôpitaux de Paris (AP-HP), Ambroise Paré Hospital, University Hospital Group Paris Saclay, Boulogne-Billancourt, France.
Insights
Cognitive impairment (CI) in chronic kidney disease (CKD) patients with low Mini-Mental State Examination (MMSE) scores (< 24) indicates a higher risk of mortality, kidney replacement therapy, and major adverse cardiovascular events (MACEs). Early CI detection can personalize CKD management.
Area of Science:
- Nephrology
- Neurology
- Epidemiology
Background:
- Cognitive impairment (CI) negatively impacts chronic disease self-management, affecting decision-making, care adherence, and mortality.
- The specific influence of CI on adverse outcomes in chronic kidney disease (CKD) is not well understood.
Purpose of the Study:
- To investigate the association between cognitive impairment and adverse clinical outcomes in patients with CKD.
- To determine the prognostic value of cognitive function assessment in CKD management.
Main Methods:
- The French CKD - Renal Epidemiology and Information Network (CKD-REIN) cohort included 3033 patients with CKD stages 2-5.
- Cognitive impairment was assessed using the Mini-Mental State Examination (MMSE).
- Cox models analyzed risks for all-cause mortality, kidney replacement therapy (KRT) initiation, and major adverse cardiovascular (CV) events (MACEs).
Main Results:
- In a cohort of 3004 CKD patients (mean eGFR: 34 ml/min/1.73 m²), 13% had MMSE scores < 24.
- Patients with MMSE < 24 showed significantly higher risks of KRT initiation (HR: 1.42), all-cause mortality (HR: 1.57), and MACEs (HR: 1.32) compared to those with MMSE > 26.
- Mild cognitive impairment (MMSE 24-26) was also linked to increased all-cause mortality (HR: 1.45).
Conclusions:
- A baseline MMSE score < 24 is a significant predictor of adverse outcomes, including mortality, KRT initiation, and MACEs in CKD patients.
- Cognitive impairment has prognostic value in CKD, suggesting that early detection can aid in personalized patient management.
- Integrating cognitive function assessment may improve the management of kidney and cardiovascular complications in CKD.
Introduction:
Cognitive impairment (CI) affects self-management in chronic diseases, leading to poor decision-making, delayed care, and increased mortality. The specific impact of CI on adverse outcomes in chronic kidney disease (CKD) remains poorly explored.
Methods:
The French CKD - Renal Epidemiology and Information Network (CKD-REIN) cohort included 3033 patients with CKD stage 2 to 5 and 5 years of follow-up. CI was assessed using the Mini-Mental State Examination (MMSE), and estimated glomerular filtration rate (eGFR) was estimated using the CKD Epidemiology Collaboration creatinine equation. Cox models evaluated the risks of all-cause mortality, kidney replacement therapy (KRT) initiation, and major adverse cardiovascular (CV) events (MACEs).
Results:
A total of 3004 patients were included in the analysis (mean age: 67 years, mean eGFR: 34 ml/min per 1.73 m2), and 64%, 23%, and 13%, respectively had MMSE scores > 26, from 24 to 26, and < 24 at baseline. During the follow-up period (mean: 3.87 years), 21.5% of patients initiated KRT, 13.4% died, and 15.3% experienced a MACE before KRT or non-CV death. In adjusted Cox models, patients with a MMSE < 24 had a higher risk of clinical adverse outcome, relative to those with a MMSE > 26: hazard ratio (HR) [95% confidence interval] was 1.42 [1.12-1.81], 1.57 [1.19-2.07], and 1.32 [1.02-1.70] for KRT initiation, all-cause mortality, and MACE, respectively. In addition, CI was associated with all-cause mortality in the MMSE of 24 to 26 group (HR: 1.45, 95% confidence interval: 1.15-1.83).
Conclusion:
In CKD, a baseline MMSE score < 24 predicts higher overall-death, KRT initiation, and MACEs, relative to a baseline score > 26. These results highlight CI's prognostic value, and suggest that earlier detection could better personalize management, particularly for kidney and CV complications.
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