Hypertension and Kidney Function After Living Kidney Donation.


Journal

JAMA
ISSN: 1538-3598
Titre abrégé: JAMA
Pays: United States
ID NLM: 7501160

Informations de publication

Date de publication:
23 May 2024
Historique:
medline: 23 5 2024
pubmed: 23 5 2024
entrez: 23 5 2024
Statut: aheadofprint

Résumé

Recent guidelines call for better evidence on health outcomes after living kidney donation. To determine the risk of hypertension in normotensive adults who donated a kidney compared with nondonors of similar baseline health. Their rates of estimated glomerular filtration rate (eGFR) decline and risk of albuminuria were also compared. Prospective cohort study of 924 standard-criteria living kidney donors enrolled before surgery and a concurrent sample of 396 nondonors. Recruitment occurred from 2004 to 2014 from 17 transplant centers (12 in Canada and 5 in Australia); follow-up occurred until November 2021. Donors and nondonors had the same annual schedule of follow-up assessments. Inverse probability of treatment weighting on a propensity score was used to balance donors and nondonors on baseline characteristics. Living kidney donation. Hypertension (systolic blood pressure [SBP] ≥140 mm Hg, diastolic blood pressure [DBP] ≥90 mm Hg, or antihypertensive medication), annualized change in eGFR (starting 12 months after donation/simulated donation date in nondonors), and albuminuria (albumin to creatinine ratio ≥3 mg/mmol [≥30 mg/g]). Among the 924 donors, 66% were female; they had a mean age of 47 years and a mean eGFR of 100 mL/min/1.73 m2. Donors were more likely than nondonors to have a family history of kidney failure (464/922 [50%] vs 89/394 [23%], respectively). After statistical weighting, the sample of nondonors increased to 928 and baseline characteristics were similar between the 2 groups. During a median follow-up of 7.3 years (IQR, 6.0-9.0), in weighted analysis, hypertension occurred in 161 of 924 donors (17%) and 158 of 928 nondonors (17%) (weighted hazard ratio, 1.11 [95% CI, 0.75-1.66]). The longitudinal change in mean blood pressure was similar in donors and nondonors. After the initial drop in donors' eGFR after nephrectomy (mean, 32 mL/min/1.73 m2), donors had a 1.4-mL/min/1.73 m2 (95% CI, 1.2-1.5) per year lesser decline in eGFR than nondonors. However, more donors than nondonors had an eGFR between 30 and 60 mL/min/1.73 m2 at least once in follow-up (438/924 [47%] vs 49/928 [5%]). Albuminuria occurred in 132 of 905 donors (15%) and 95 of 904 nondonors (11%) (weighted hazard ratio, 1.46 [95% CI, 0.97-2.21]); the weighted between-group difference in the albumin to creatinine ratio was 1.02 (95% CI, 0.88-1.19). In this cohort study of living kidney donors and nondonors with the same follow-up schedule, the risks of hypertension and albuminuria were not significantly different. After the initial drop in eGFR from nephrectomy, donors had a slower mean rate of eGFR decline than nondonors but were more likely to have an eGFR between 30 and 60 mL/min/1.73 m2 at least once in follow-up. ClinicalTrials.gov Identifier: NCT00936078.

Identifiants

pubmed: 38780499
pii: 2819311
doi: 10.1001/jama.2024.8523
doi:

Banques de données

ClinicalTrials.gov
['NCT00936078']

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Auteurs

Amit X Garg (AX)

Lawson Health Research Institute and London Health Sciences, London, Ontario, Canada.
ICES, Ontario, Canada.
Department of Epidemiology and Biostatistics, Schulich School of Medicine and Dentistry, Western University, London, Ontario, Canada.
Division of Nephrology, Department of Medicine, Schulich School of Medicine and Dentistry, Western University, London, Ontario, Canada.
Department of Research Methods, Evidence and Uptake, Faculty of Health Sciences, McMaster University, Hamilton, Ontario, Canada.
Ontario Renal Network, Ontario Health, Toronto, Ontario, Canada.

Jennifer B Arnold (JB)

Lawson Health Research Institute and London Health Sciences, London, Ontario, Canada.

Meaghan S Cuerden (MS)

Lawson Health Research Institute and London Health Sciences, London, Ontario, Canada.

Christine Dipchand (C)

Department of Medicine (Nephrology), Queen Elizabeth II Health Sciences Centre and Dalhousie University Halifax, Nova Scotia, Canada.

Liane S Feldman (LS)

Department of Surgery, McGill University, Montreal, Quebec, Canada.

John S Gill (JS)

University of British Columbia, Vancouver, British Columbia, Canada.

Martin Karpinski (M)

University of Manitoba, Winnipeg, Manitoba, Canada.

Scott Klarenbach (S)

University of Alberta, Edmonton, Alberta, Canada.

Greg Knoll (G)

Department of Medicine (Nephrology), the Ottawa Hospital and University of Ottawa, Ottawa, Ontario, Canada.

Charmaine E Lok (CE)

University Health Network, Toronto, Ontario, Canada.

Matthew Miller (M)

St Joseph's Healthcare, Hamilton, Ontario, Canada.

Mauricio Monroy-Cuadros (M)

University of Calgary, Calgary, Alberta, Canada.

Christopher Nguan (C)

University of British Columbia, Vancouver, British Columbia, Canada.

G V Ramesh Prasad (GVR)

St Michael's Hospital, University of Toronto, Toronto, Ontario, Canada.
University of Toronto, Toronto, Ontario, Canada.

Jessica M Sontrop (JM)

Lawson Health Research Institute and London Health Sciences, London, Ontario, Canada.
Department of Epidemiology and Biostatistics, Schulich School of Medicine and Dentistry, Western University, London, Ontario, Canada.

Leroy Storsley (L)

University of Manitoba, Winnipeg, Manitoba, Canada.

Neil Boudville (N)

Medical School, The University of Western Australia, Nedlands, Western Australia, Australia.
Department of Renal Medicine, Sir Charles Gairdner Hospital, Nedlands, Western Australia, Australia.

Classifications MeSH