TY - JOUR
T1 - Impact of declining renal function on outcomes in pulmonary arterial hypertension
T2 - A REVEAL registry analysis
AU - Chakinala, Murali M.
AU - Coyne, Daniel W.
AU - Benza, Raymond L.
AU - Frost, Adaani E.
AU - McGoon, Michael D.
AU - Hartline, Brian K.
AU - Frantz, Robert P.
AU - Selej, Mona
AU - Zhao, Carol
AU - Mink, David R.
AU - Farber, Harrison W.
N1 - Funding Information:
M.C. has received consulting fees, speaker fees and/or grant monies from Actelion, Gilead, United Therapeutics, Bayer, Medtronic, Novartis AG, Ikaria and Reata Pharmaceuticals, and is a board or advisory committee member for Actelion, Gilead, Bayer, United Therapeutics, SteadyMed Therapeutics and Express Scripts. D.C. is a consultant or advisor for Fresenius Medical Care–Renal Group, Vifor, Eli Lilly, Medibeacon and Aspire, and has received speaker fees and/or grant support from Fresenius Medical Care–Renal Group, Hospira/Pfizer, Fibrogen, ZS Pharma and Eli Lilly. R.B. is a member of the steering committee, board or advisory committee for Bayer, Bellerophon and United Therapeutics/Lung LLC, and receives research support from Gilead, Actelion, United Therapeutics and Bellerophon. A.F. is a consultant and board member for Gilead and Actelion, and has received speaker fees and/or grant support from Gilead, Actelion, Bayer, United Therapeutics, Lung LLC, Reata and Novartis. M.M. serves on a steering committee for LungBiotechnology and a data monitoring committee for Pfizer. R.F. has served as a steering committee and advisory board member for Actelion. M.S. is an employee of Actelion Pharmaceuticals US, Inc., and owns stock in Actelion Pharmaceuticals. C.Z. is an employee of Actelion Pharmaceuticals, US, Inc., and owns stock in Actelion. B.H. is an employee of Actelion Pharmaceuticals, US, Inc., and owns stock in Actelion. D.M. is an employee of ICON Clinical Research. H.F. has served as a speaker/and or steering committee member for Gilead, Bayer, Actelion, Bellerophon and United Therapeutics/Lung, LLC, and has received research support from Gilead, Actelion and United Therapeutics. Actelion Pharmaceuticals, US, Inc., is the sponsor of the REVEAL and provided funding and support for this study. Statistical analyses were performed by ICON plc (funded by Actelion Pharmaceuticals US, Inc). Editorial support was provided by AlphaBioCom LLC and Twist Medical LLC (funded by Actelion Pharmaceuticals US, Inc.).
Publisher Copyright:
© 2018 International Society for the Heart and Lung Transplantation
PY - 2018/6
Y1 - 2018/6
N2 - Background: Renal dysfunction is associated with abnormal cardiopulmonary hemodynamics, in-hospital death and poor survival in patients with pulmonary arterial hypertension (PAH), and thus it may be a prognostic biomarker. In our analysis we assess the relationship between change in estimated glomerular filtration rate (eGFR) and outcomes in PAH patients in the Registry to Evaluate Early and Long-term PAH Disease Management (REVEAL). Methods: Overall 2,368 patients were classified into chronic kidney disease (CKD) stages based on baseline eGFR: normal or Stages 1 or 2 (n = 1,699); Stage 3a (n = 399); Stage 3b (n = 196); and Stages 4 or 5 (n = 74). We evaluated the relationship between baseline CKD stage and survival, as well as the composite end-point of survival and freedom from all-cause hospitalization. The relationships between change in eGFR at ≥1 year and these clinical end-points were also evaluated. Results: Patients with a ≥10% decline in eGFR from baseline over ≥1 year had a significantly increased risk of death (hazard ratio 1.66; p < 0.0001) and the composite of all-cause hospitalization and death (hazard ratio 1.33; p = 0.002). This decline predicted survival independently of changes in 6-minute walk distance and functional class. However, a ≥10% increase in eGFR was not significantly associated with either end-point. Conclusion: In REVEAL, a ≥10% decline in eGFR over ≥1 year independently predicted poorer survival. Thus, eGFR may be a simple and economical biomarker in PAH.
AB - Background: Renal dysfunction is associated with abnormal cardiopulmonary hemodynamics, in-hospital death and poor survival in patients with pulmonary arterial hypertension (PAH), and thus it may be a prognostic biomarker. In our analysis we assess the relationship between change in estimated glomerular filtration rate (eGFR) and outcomes in PAH patients in the Registry to Evaluate Early and Long-term PAH Disease Management (REVEAL). Methods: Overall 2,368 patients were classified into chronic kidney disease (CKD) stages based on baseline eGFR: normal or Stages 1 or 2 (n = 1,699); Stage 3a (n = 399); Stage 3b (n = 196); and Stages 4 or 5 (n = 74). We evaluated the relationship between baseline CKD stage and survival, as well as the composite end-point of survival and freedom from all-cause hospitalization. The relationships between change in eGFR at ≥1 year and these clinical end-points were also evaluated. Results: Patients with a ≥10% decline in eGFR from baseline over ≥1 year had a significantly increased risk of death (hazard ratio 1.66; p < 0.0001) and the composite of all-cause hospitalization and death (hazard ratio 1.33; p = 0.002). This decline predicted survival independently of changes in 6-minute walk distance and functional class. However, a ≥10% increase in eGFR was not significantly associated with either end-point. Conclusion: In REVEAL, a ≥10% decline in eGFR over ≥1 year independently predicted poorer survival. Thus, eGFR may be a simple and economical biomarker in PAH.
KW - REVEAL
KW - biomarker
KW - chronic kidney disease
KW - glomerular filtration rate
KW - pulmonary arterial hypertension
KW - serum creatinine
UR - http://www.scopus.com/inward/record.url?scp=85034665309&partnerID=8YFLogxK
U2 - 10.1016/j.healun.2017.10.028
DO - 10.1016/j.healun.2017.10.028
M3 - Article
C2 - 29174533
AN - SCOPUS:85034665309
SN - 1053-2498
VL - 37
SP - 696
EP - 705
JO - Journal of Heart and Lung Transplantation
JF - Journal of Heart and Lung Transplantation
IS - 6
ER -