4.5 Article

Predictors and significance of kidney dysfunction in patients with chronic graft-versus-host disease

Journal

BONE MARROW TRANSPLANTATION
Volume -, Issue -, Pages -

Publisher

SPRINGERNATURE
DOI: 10.1038/s41409-023-02032-1

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The study aimed to investigate kidney complications in patients with chronic graft-versus-host disease (cGVHD). The research found that kidney dysfunction was present in a subgroup of cGVHD patients, with some specific factors associated with this dysfunction. It was also observed that kidney dysfunction was linked to lower overall survival in these patients, highlighting the significance of addressing this complication. The study suggests that the etiology of kidney dysfunction in cGVHD patients may be unrelated to the disease itself but potentially caused by drug-related toxicities.
Kidney complications have been studied in allogeneic hematopoietic stem cell transplant patients but not specifically among chronic graft-versus-host disease (cGVHD) patients. Participants (n = 365) enrolled in the cross-sectional cGVHD natural history study (NCT00092235) were assessed for kidney dysfunction and overall survival. Kidney dysfunction was analyzed for associations in univariate and multivariable analyses. Kidney dysfunction (eGFR < 60) was found in 64 patients, and 29 patients had moderate-severe kidney dysfunction (eGFR < 45). Patients with kidney dysfunction were more likely treated with cyclosporine at evaluation or to have received it for GVHD prophylaxis, or prior treatment of GVHD. Patients with kidney dysfunction were less severely affected by cGVHD of skin, mouth, and joints/fascia. In multivariable modeling, history of cyclosporine use (OR = 2.19, 95% CI 1.13-4.25), angiotensin receptor blocker use (OR = 5.57, 95% CI 1.49-20.84), proteinuria (OR = 2.39, 95% CI 1.19-4.79), lower CRP (OR = 0.95, 95% CI 0.91-0.99), lower C3 (OR = 0.98, 95% CI 0.97-0.99), and lower hemoglobin (OR = 0.70, 95% CI 0.58-0.84) were jointly associated with kidney dysfunction. Overall survival was lower in those with moderate-severe kidney dysfunction (p = 0.015), demonstrating the importance of addressing kidney dysfunction in this population. The association of kidney dysfunction with less severe cGVHD suggests an etiology unrelated to cGVHD but potentially a consequence of drug-related toxicities.

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