Predictors and significance of kidney dysfunction in patients with chronic graft-versus-host disease
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...
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Published in | Bone marrow transplantation (Basingstoke) Vol. 58; no. 10; pp. 1112 - 1120 |
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Main Authors | , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
London
Nature Publishing Group UK
01.10.2023
Nature Publishing Group |
Subjects | |
Online Access | Get full text |
ISSN | 0268-3369 1476-5365 1476-5365 |
DOI | 10.1038/s41409-023-02032-1 |
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Summary: | 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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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 Concept of study: SZP, NGH, MAW, DB, and FP; data collection: SZP, NGH, MAW, JWM, EWC, LEC, GOJ, and MTM; data analysis: SMS, DB, and FP; draft, review, approval of manuscript: all authors. AUTHOR CONTRIBUTIONS |
ISSN: | 0268-3369 1476-5365 1476-5365 |
DOI: | 10.1038/s41409-023-02032-1 |