Cohort study demonstrates stable long-term renal function in living kidney donors, highlighting that baseline comorbidities impact outcomes more than chronological age.
Living kidney donation achieves excellent recipient outcomes, but increasingly involves older and medically complex donors, while long-term data across age groups remain limited. The Heidelberg Kidney Donor Study followed 632 donors (1991–2020), stratified by age <40 (n = 93), 40–60 (n = 424), and >60 years (n = 115). Primary outcomes were a ≥50% eGFR decline and an eGFR <45 mL/min/1.73 m 2 at long-term follow-up. Early post-donation adaptation, long-term eGFR trajectories, cardiovascular events, and risk patterns were evaluated. Mean donor age was 50.6 ± 10.6 years (62.5% female). eGFR declined by 26.0% after donation and remained stable thereafter. At a median follow-up of 12 years, ≥50% eGFR decline occurred in 4.8%, 5.3%, and 14.4% of donors aged <40, 40–60, and >60 years, respectively, an eGFR <45 mL/min/1.73 m 2 in 1.2%, 5.3%, and 20.4%. An eGFR <30 mL/min/1.73 m 2 occurred in 1.2%, major adverse cardiovascular events in 4.3%. Age, hypertension, and baseline-eGFR independently predicted renal impairment. Younger donors with hypertension or obesity had up to a 14.3% risk of ≥50% eGFR decline, exceeding the risk in healthy older donors (12.5%). Living kidney donation was associated with stable long-term kidney function after early adaptation, with substantial heterogeneity driven more by baseline renal reserve and comorbidity than chronological age alone.
No takes yet. Share an insight, caveat, or question.
Sommerer et al. (2026) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: