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Development and Validation of Prediction Models of Adverse Kidney Outcomes in the Population With and Without Diabetes.
Grams, Morgan E; Brunskill, Nigel J; Ballew, Shoshana H; Sang, Yingying; Coresh, Josef; Matsushita, Kunihiro; Surapaneni, Aditya; Bell, Samira; Carrero, Juan J; Chodick, Gabriel; Evans, Marie; Heerspink, Hiddo J L; Inker, Lesley A; Iseki, Kunitoshi; Kalra, Philip A; Kirchner, H Lester; Lee, Brian J; Levin, Adeera; Major, Rupert W; Medcalf, James; Nadkarni, Girish N; Naimark, David M J; Ricardo, Ana C; Sawhney, Simon; Sood, Manish M; Staplin, Natalie; Stempniewicz, Nikita; Stengel, Benedicte; Sumida, Keiichi; Traynor, Jamie P; van den Brand, Jan; Wen, Chi-Pang; Woodward, Mark; Yang, Jae Won; Wang, Angela Yee-Moon; Tangri, Navdeep.
Affiliation
  • Grams ME; Department of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD.
  • Brunskill NJ; Division of Precision of Medicine, Department of Medicine, New York University Grossman School of Medicine, New York, NY.
  • Ballew SH; Department of Cardiovascular Sciences, University of Leicester, Leicester, U.K.
  • Sang Y; John Walls Renal Unit, Leicester General Hospital, University Hospitals of Leicester NHS Trust, Leicester, U.K.
  • Coresh J; Department of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD.
  • Matsushita K; Department of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD.
  • Surapaneni A; Department of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD.
  • Bell S; Department of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD.
  • Carrero JJ; Department of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD.
  • Chodick G; Renal Unit, Ninewells Hospital, Dundee, U.K.
  • Evans M; Division of Population Health and Genomics, School of Medicine, University of Dundee, Dundee, U.K.
  • Heerspink HJL; Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Huddinge, Sweden.
  • Inker LA; Medical Division, Maccabi Healthcare Services, and Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
  • Iseki K; Department of Clinical Intervention, and Technology, Karolinska University Hospital and Karolinska Institutet, Stockholm, Sweden.
  • Kalra PA; Department of Clinical Pharmacy and Pharmacology, University of Groningen, University Medical Center, Groningen, Netherlands.
  • Kirchner HL; Tufts Medical Center, Boston, MA.
  • Lee BJ; Okinawa Heart and Renal Association, Okinawa, Japan.
  • Levin A; Department of Renal Medicine, Salford Royal NHS Foundation Trust, Salford, U.K.
  • Major RW; Department of Population Health Sciences, Geisinger, Danville, PA.
  • Medcalf J; Kaiser Permanente, Hawaii Region, and Moanalua Medical Center, Honolulu, HI.
  • Nadkarni GN; Division of Nephrology, University of British Columbia, Vancouver, British Columbia, Canada.
  • Naimark DMJ; John Walls Renal Unit, Leicester General Hospital, University Hospitals of Leicester NHS Trust, Leicester, U.K.
  • Ricardo AC; Department of Health Sciences, University of Leicester, Leicester, U.K.
  • Sawhney S; John Walls Renal Unit, Leicester General Hospital, University Hospitals of Leicester NHS Trust, Leicester, U.K.
  • Sood MM; UK Renal Registry, The Renal Association, Bristol, U.K.
  • Staplin N; Department of Cardiovascular Sciences, University of Leicester, Leicester, U.K.
  • Stempniewicz N; Division of Nephrology, Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, NY.
  • Stengel B; Sunnybrook Hospital, University of Toronto, Toronto, Ontario, Canada.
  • Sumida K; Department of Medicine, University of Illinois, Chicago, IL.
  • Traynor JP; Aberdeen Centre for Health Data Science, University of Aberdeen, Aberdeen, U.K.
  • van den Brand J; Division of Nephrology, Department of Medicine, University of Ottawa, Ottawa, Ontario, Canada.
  • Wen CP; Clinical Epidemiology Program, Ottawa Hospital Research Institute, Ottawa, Ontario, Canada.
  • Woodward M; Division of Nephrology, Department of Medicine, The Ottawa Hospital, Ottawa, Ontario, Canada.
  • Yang JW; MRC Population Health Research Unit, Clinical Trial Service Unit and Epidemiological Studies Unit, Nuffield Department of Population Health, Oxford, U.K.
  • Wang AY; American Medical Group Association, Alexandria, VA.
  • Tangri N; University Paris-Saclay, University of Versailles Saint-Quentin-en-Yvelines, INSERM, Clinical Epidemiology Team, Centre for Epidemiology and Population Health, Villejuif, France.
Diabetes Care ; 45(9): 2055-2063, 2022 09 01.
Article in En | MEDLINE | ID: mdl-35856507
ABSTRACT

OBJECTIVE:

To predict adverse kidney outcomes for use in optimizing medical management and clinical trial design. RESEARCH DESIGN AND

METHODS:

In this meta-analysis of individual participant data, 43 cohorts (N = 1,621,817) from research studies, electronic medical records, and clinical trials with global representation were separated into development and validation cohorts. Models were developed and validated within strata of diabetes mellitus (presence or absence) and estimated glomerular filtration rate (eGFR; ≥60 or <60 mL/min/1.73 m2) to predict a composite of ≥40% decline in eGFR or kidney failure (i.e., receipt of kidney replacement therapy) over 2-3 years.

RESULTS:

There were 17,399 and 24,591 events in development and validation cohorts, respectively. Models predicting ≥40% eGFR decline or kidney failure incorporated age, sex, eGFR, albuminuria, systolic blood pressure, antihypertensive medication use, history of heart failure, coronary heart disease, atrial fibrillation, smoking status, and BMI, and, in those with diabetes, hemoglobin A1c, insulin use, and oral diabetes medication use. The median C-statistic was 0.774 (interquartile range [IQR] = 0.753, 0.782) in the diabetes and higher-eGFR validation cohorts; 0.769 (IQR = 0.758, 0.808) in the diabetes and lower-eGFR validation cohorts; 0.740 (IQR = 0.717, 0.763) in the no diabetes and higher-eGFR validation cohorts; and 0.750 (IQR = 0.731, 0.785) in the no diabetes and lower-eGFR validation cohorts. Incorporating the previous 2-year eGFR slope minimally improved model performance, and then only in the higher-eGFR cohorts.

CONCLUSIONS:

Novel prediction equations for a decline of ≥40% in eGFR can be applied successfully for use in the general population in persons with and without diabetes with higher or lower eGFR.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Diabetes Mellitus / Renal Insufficiency / Renal Insufficiency, Chronic Type of study: Prognostic_studies / Risk_factors_studies / Systematic_reviews Limits: Humans Language: En Journal: Diabetes Care Year: 2022 Document type: Article Affiliation country: Moldova

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Diabetes Mellitus / Renal Insufficiency / Renal Insufficiency, Chronic Type of study: Prognostic_studies / Risk_factors_studies / Systematic_reviews Limits: Humans Language: En Journal: Diabetes Care Year: 2022 Document type: Article Affiliation country: Moldova