TY - JOUR
T1 - Contemporary incidence and risk factors of post transplant Erythrocytosis in deceased donor kidney transplantation
AU - Alasfar, Sami
AU - Hall, Isaac E.
AU - Mansour, Sherry G.
AU - Jia, Yaqi
AU - Thiessen-Philbrook, Heather R.
AU - Weng, Francis L.
AU - Singh, Pooja
AU - Schröppel, Bernd
AU - Muthukumar, Thangamani
AU - Mohan, Sumit
AU - Malik, Rubab F.
AU - Harhay, Meera N.
AU - Doshi, Mona D.
AU - Akalin, Enver
AU - Bromberg, Jonathan S.
AU - Brennan, Daniel C.
AU - Reese, Peter P.
AU - Parikh, Chirag R.
N1 - Funding Information:
S.G. Mansour: supported by the American Heart Association (18CDA34110151) and Patterson Trust Fund.
Funding Information:
E. Akalin. Grant support from CareDx and NIH.
Funding Information:
I.E. Hall: NIH grant support from NCATS (UL1TR002538 and KL2TR002539).
Funding Information:
P.P. Reese: Epidemiology consulting from COHRDATA related to dialysis outcomes. Grant/Research Support from Merck, CVS. Initiated grants from Merck to the University of Pennsylvania to support the THINKER (kidney), USHER (heart) and SHELTER (lung) trials of transplanting organs from donors with Hepatitis C into Hepatitis C negative recipients. Initiated grants from CVS to the University of Pennsylvania to support studies of medication adherence. Associate Editor, American Journal of Kidney Disease.
Funding Information:
S. Alasfar: Grant support from CareDx, Shire, and NIH.
Funding Information:
This work was supported by the National Institutes of Health (NIH)/National Institutes of Diabetes and Digestive and Kidney Diseases (NIDDK) grant R01DK-93770 and grant K24DK090203 to Dr. Parikh; George M. O’Brien Kidney Center at Yale Grant P30DK079310 to Dr. Parikh; a grant to Dr. Hall by the NIH/National Center for Advancing Translational Sciences (NCATS) under award numbers UL1TR002538 and KL2TR002539.
Publisher Copyright:
© 2021, The Author(s).
PY - 2021/12
Y1 - 2021/12
N2 - Background: Post-Transplant erythrocytosis (PTE) has not been studied in large recent cohorts. In this study, we evaluated the incidence, risk factors, and outcome of PTE with current transplant practices using the present World Health Organization criteria to define erythrocytosis. We also tested the hypothesis that the risk of PTE is greater with higher-quality kidneys. Methods: We utilized the Deceased Donor Study which is an ongoing, multicenter, observational study of deceased donors and their kidney recipients that were transplanted between 2010 and 2013 across 13 centers. Eryrthocytosis is defined by hemoglobin> 16.5 g/dL in men and> 16 g/dL in women. Kidney quality is measured by Kidney Donor Profile Index (KDPI). Results: Of the 1123 recipients qualified to be in this study, PTE was observed at a median of 18 months in 75 (6.6%) recipients. Compared to recipients without PTE, those with PTE were younger [mean 48±11 vs 54±13 years, p < 0.001], more likely to have polycystic kidney disease [17% vs 6%, p < 0.001], have received kidneys from younger donors [36 ±13 vs 41±15 years], and be on RAAS inhibitors [35% vs 22%, p < 0.001]. Recipients with PTE were less likely to have received kidneys from donors with hypertension [16% vs 32%, p = 0.004], diabetes [1% vs 11%, p = 0.008], and cerebrovascular event (24% vs 36%, p = 0.036). Higher KDPI was associated with decreased PTE risk [HR 0.98 (95% CI: 0.97–0.99)]. Over 60 months of follow-up, only 17 (36%) recipients had sustained PTE. There was no association between PTE and graft failure or mortality, Conclusions: The incidence of PTE was low in our study and PTE resolved in majority of patients. Lower KDPI increases risk of PTE. The underutilization of RAAS inhibitors in PTE patients raises the possibility of under-recognition of this phenomenon and should be explored in future studies.
AB - Background: Post-Transplant erythrocytosis (PTE) has not been studied in large recent cohorts. In this study, we evaluated the incidence, risk factors, and outcome of PTE with current transplant practices using the present World Health Organization criteria to define erythrocytosis. We also tested the hypothesis that the risk of PTE is greater with higher-quality kidneys. Methods: We utilized the Deceased Donor Study which is an ongoing, multicenter, observational study of deceased donors and their kidney recipients that were transplanted between 2010 and 2013 across 13 centers. Eryrthocytosis is defined by hemoglobin> 16.5 g/dL in men and> 16 g/dL in women. Kidney quality is measured by Kidney Donor Profile Index (KDPI). Results: Of the 1123 recipients qualified to be in this study, PTE was observed at a median of 18 months in 75 (6.6%) recipients. Compared to recipients without PTE, those with PTE were younger [mean 48±11 vs 54±13 years, p < 0.001], more likely to have polycystic kidney disease [17% vs 6%, p < 0.001], have received kidneys from younger donors [36 ±13 vs 41±15 years], and be on RAAS inhibitors [35% vs 22%, p < 0.001]. Recipients with PTE were less likely to have received kidneys from donors with hypertension [16% vs 32%, p = 0.004], diabetes [1% vs 11%, p = 0.008], and cerebrovascular event (24% vs 36%, p = 0.036). Higher KDPI was associated with decreased PTE risk [HR 0.98 (95% CI: 0.97–0.99)]. Over 60 months of follow-up, only 17 (36%) recipients had sustained PTE. There was no association between PTE and graft failure or mortality, Conclusions: The incidence of PTE was low in our study and PTE resolved in majority of patients. Lower KDPI increases risk of PTE. The underutilization of RAAS inhibitors in PTE patients raises the possibility of under-recognition of this phenomenon and should be explored in future studies.
KW - Erythrocytosis
KW - Hemoglobin
KW - KDPI
KW - Kidney transplant
UR - http://www.scopus.com/inward/record.url?scp=85099277716&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85099277716&partnerID=8YFLogxK
U2 - 10.1186/s12882-021-02231-2
DO - 10.1186/s12882-021-02231-2
M3 - Article
C2 - 33435916
AN - SCOPUS:85099277716
SN - 1471-2369
VL - 22
JO - BMC Nephrology
JF - BMC Nephrology
IS - 1
M1 - 26
ER -