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The Brain in Kidney Disease (BRINK) Cohort Study: Design and Baseline Cognitive Function.
Murray, Anne M; Bell, Elizabeth J; Tupper, David E; Davey, Cynthia S; Pederson, Sarah L; Amiot, Elizabeth M; Miley, Kathleen M; McPherson, Lauren; Heubner, Brooke M; Gilbertson, David T; Foley, Robert N; Drawz, Paul E; Slinin, Yelena; Rossom, Rebecca C; Lakshminarayan, Kamakshi; Vemuri, Prashanthi; Jack, Clifford R; Knopman, David S.
Affiliation
  • Murray AM; Berman Center for Clinical Research, Minneapolis Medical Research Foundation, Minneapolis, MN; Geriatrics Division, Hennepin County Medical Center, Minneapolis, MN. Electronic address: amurray@bermancenter.org.
  • Bell EJ; Berman Center for Clinical Research, Minneapolis Medical Research Foundation, Minneapolis, MN.
  • Tupper DE; Department of Psychology and Neuropsychology, Hennepin County Medical Center, Minneapolis, MN.
  • Davey CS; Biostatistical Design and Analysis Center, University of Minnesota Clinical and Translational Science Institute, Minneapolis, MN.
  • Pederson SL; Berman Center for Clinical Research, Minneapolis Medical Research Foundation, Minneapolis, MN.
  • Amiot EM; Berman Center for Clinical Research, Minneapolis Medical Research Foundation, Minneapolis, MN.
  • Miley KM; Department of Psychiatry, Hennepin County Medical Center, Minneapolis, MN.
  • McPherson L; University of Minnesota Medical School, Minneapolis, MN.
  • Heubner BM; Chronic Disease Research Group, Minneapolis Medical Research Foundation, Hennepin County Medical Center, Minneapolis, MN.
  • Gilbertson DT; Chronic Disease Research Group, Minneapolis Medical Research Foundation, Hennepin County Medical Center, Minneapolis, MN.
  • Foley RN; Nephrology Division, Department of Medicine, University of Minnesota, Minneapolis, MN.
  • Drawz PE; Nephrology Division, Department of Medicine, University of Minnesota, Minneapolis, MN.
  • Slinin Y; Nephrology Division, Department of Medicine, University of Minnesota, Minneapolis, MN; Veterans Affairs Medical Center, Minneapolis, MN.
  • Rossom RC; HealthPartners Institute for Education and Research, Minneapolis, MN.
  • Lakshminarayan K; Neurology Department, University of Minnesota, Minneapolis, MN; Division of Epidemiology & Community Health, University of Minnesota School of Public Health, Minneapolis, MN.
  • Vemuri P; Department of Radiology, Mayo Clinic, Rochester, MN.
  • Jack CR; Department of Radiology, Mayo Clinic, Rochester, MN.
  • Knopman DS; Department of Neurology, Mayo Clinic, Rochester, MN.
Am J Kidney Dis ; 67(4): 593-600, 2016 Apr.
Article in En | MEDLINE | ID: mdl-26744128
ABSTRACT

BACKGROUND:

The Brain in Kidney Disease (BRINK) Study aims to identify mechanisms that contribute to increased risk for cognitive impairment in patients with chronic kidney disease (CKD). We describe the rationale, design, and methods of the study and report baseline recruitment and cognitive function results. STUDY

DESIGN:

Longitudinal observational cohort study of the epidemiology of cognitive impairment in CKD. The primary aim is to characterize the association between (1) baseline and incident stroke, white matter disease, estimated glomerular filtration rate (eGFR), inflammation, microalbuminuria, and dialysis initiation and (2) cognitive decline over 3 years in a CKD cohort with a mean eGFR<45 mL/min/1.73 m(2). SETTING &

PARTICIPANTS:

Community-dwelling participants 45 years or older recruited from 4 health systems into 2 groups reduced eGFR, defined as eGFR<60 mL/min/1.73 m(2) (non-dialysis dependent), and control, defined as eGFR≥60 mL/min/1.73 m(2). PREDICTOR eGFR group.

OUTCOMES:

Performance on cognitive function tests and structural brain magnetic resonance imaging. MEASUREMENTS Sequential cognitive and physical function testing, serum and urine biomarker measurement, and brain magnetic resonance images over 3 years.

RESULTS:

Of 554 participants, mean age was 69.3 years; 333, 88, and 133 had eGFRs<45 (non-dialysis dependent, nontransplantation), 45 to <60, and ≥60 (controls) mL/min/1.73 m(2), respectively. Mean eGFR in reduced-eGFR participants was 34.3 mL/min/1.73 m(2). Baseline cognitive performance was significantly associated with eGFR in all domains except language. Participants with eGFRs<30 mL/min/1.73 m(2) performed significantly worse than those with eGFRs≥30 mL/min/1.73 m(2) on tests of memory, processing speed, and executive function. Participants with reduced eGFRs overall scored worst on the Immediate Brief Visual-Spatial Memory Test-Revised.

LIMITATIONS:

Healthy cohort bias, competing risk for death versus cognitive decline.

CONCLUSIONS:

Cognitive function was significantly worse in participants with eGFRs<30 mL/min/1.73 m(2). Future BRINK analyses will measure risk factors for cognitive decline using the longitudinal data.
Subject(s)
Key words

Full text: 1 Database: MEDLINE Main subject: Cognition Disorders / Renal Insufficiency, Chronic Type of study: Etiology_studies / Incidence_studies / Observational_studies / Prevalence_studies / Prognostic_studies Limits: Aged / Female / Humans / Male / Middle aged Language: En Year: 2016 Type: Article

Full text: 1 Database: MEDLINE Main subject: Cognition Disorders / Renal Insufficiency, Chronic Type of study: Etiology_studies / Incidence_studies / Observational_studies / Prevalence_studies / Prognostic_studies Limits: Aged / Female / Humans / Male / Middle aged Language: En Year: 2016 Type: Article