Predictors of developing renal dysfunction following diagnosis of transthyretin cardiac amyloidosis

被引:2
|
作者
McDonald, Malcolm L. [1 ]
Manla, Yosef [2 ]
Sonnino, Alice [1 ]
Alonso, Mileydis [1 ]
Neicheril, Radhika K. [3 ]
Sanchez, Alejandro [1 ]
Lafave, Gabrielle [2 ]
De Armas, Yelenis Seijo [1 ]
Camargo, Antonio Lewis [1 ]
Uppal, Dipan [1 ]
Handa, Armaan [1 ]
Wolinsky, David [1 ]
Rivera, Nina Thakkar [1 ]
Velez, Mauricio [1 ]
Baran, David A. [1 ]
Estep, Jerry D. [1 ]
Snipelisky, David [1 ,4 ]
机构
[1] Cleveland Clin Florida, Dept Cardiothorac Surg, Heart Vasc & Thorac Inst, Weston, FL USA
[2] Cleveland Clin Abu Dhabi, Heart Vasc & Thorac Inst, Dept Cardiol, Abu Dhabi, U Arab Emirates
[3] Cleveland Clin Florida, Dept Med, Internal Med, Weston, FL USA
[4] Cleveland Clin, Robert & Suzanne Tomsich Dept Cardiol, Sect Heart Failure & Cardiac Transplant Med, 2950 Cleveland Clin Blvd, Weston, FL 33331 USA
关键词
ATTR; cardiac amyloidosis; renal outcomes; SGLT-2; inhibitor; DISEASE;
D O I
10.1002/clc.24298
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BackgroundIn patients with transthyretin cardiac amyloidosis (ATTR-CA), renal dysfunction is a poor prognostic indicator. Limited data are available on variables that portend worsening renal function (wRF) among ATTR-CA patients.ObjectivesThis study assesses which characteristics place patients at higher risk for the development of wRF (defined as a drop of >= 10% in glomerular filtration rate [GFR]) within the first year following diagnosis of ATTR-CA.MethodsWe included patients with ATTR-CA (n = 134) evaluated between 2/2016 and 12/2022 and followed for up to 1 year at our amyloid clinic. Patients were stratified into two groups: a group with maintained renal function (mRF) and a group with wRF and compared using appropriate testing. Significant variables in the univariate analysis were included in the multivariable logistic regression model to determine characteristics associated with wRF.ResultsWithin a follow-up period of 326 +/- 118 days, the median GFR% change measured -6% [-18%, +8]. About 41.8% (n = 56) had wRF, while the remainder had mRF. In addition, in patients with no prior history of chronic kidney disease (CKD), 25.5% developed de novo CKD. On multivariable logistic regression, only New York Heart Association (NYHA) class >= III (odds ratio [OR]: 3.9, 95% confidence interval [CI]: [1.6-9.3]), history of ischemic heart disease (IHD) (OR: 0.3, 95% CI: [0.1-0.7]), and not receiving SGLT-2i (OR: 0.1, 95% CI: [0.02-0.5]) were significant predictors of wRF.ConclusionOur study demonstrated that the development of de novo renal dysfunction or wRF is common following the diagnosis of ATTR-CA. Additionally, we identified worse NYHA class and no prior history of IHD as significant predictors associated with developing wRF, while receiving SGLT-2i therapy appeared to be protective in this population. Our study demonstrated that the development of de novo renal dysfunction or worsening renal function is common following the diagnosis of ATTR-CA. Additionally, we identified worse NYHA class and no history of IHD as significant predictors associated with developing worsening renal function, while receiving SGLT2i therapy appeared to be protective. image
引用
收藏
页数:8
相关论文
共 50 条
  • [31] Transthyretin cardiac amyloidosis
    Porcari, Aldostefano
    Fontana, Marianna
    Gillmore, Julian D.
    CARDIOVASCULAR RESEARCH, 2023, 118 (18) : 3517 - 3535
  • [32] Cardiac transthyretin amyloidosis
    Dungu, Jason N.
    Anderson, Lisa J.
    Whelan, Carol J.
    Hawkins, Philip N.
    HEART, 2012, 98 (21) : 1546 - 1554
  • [33] Transthyretin Cardiac Amyloidosis
    Mankad, Anit K.
    Shah, Keyur B.
    CURRENT CARDIOLOGY REPORTS, 2017, 19 (10)
  • [34] Echocardiography C phenotype and independent predictors of prognosis in transthyretin cardiac amyloidosis
    Martone, Raffaele
    Chacko, Liza
    Bandera, Francesco
    Boldrini, Michele
    Quarta, Cristina
    Cappelli, Francesco
    Guazzi, Marco
    Hawkins, Philip N.
    Gillmore, Julian D.
    Fontana, Marianna
    EUROPEAN HEART JOURNAL SUPPLEMENTS, 2019, 21 (0J) : J183 - J183
  • [35] Developing Therapy for Transthyretin Amyloidosis
    Campbell, Courtney M.
    Zhang, Kathleen
    Lenihan, Daniel J.
    Witteles, Ronald
    AMERICAN JOURNAL OF MEDICINE, 2022, 135 : S44 - S48
  • [36] PREDICTORS OF VENTRICULAR ARRHYTHMIA AND APPROPRIATE DEVICE THERAPY IN TRANSTHYRETIN CARDIAC AMYLOIDOSIS
    Patel, Rahul
    Steinberg, Rebecca S.
    Rim, Austin
    Yalamanchili, Sreeram
    Brown, Matthew T.
    Bhatt, Kunal
    JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2023, 81 (08) : 643 - 643
  • [37] Diagnosis and Treatment of Transthyretin Cardiac Amyloidosis. Progress and Hope
    Gonzalez-Lopez, Esther
    Lopez-Sainz, Angela
    Garcia-Pavia, Pablo
    REVISTA ESPANOLA DE CARDIOLOGIA, 2017, 70 (11): : 991 - 1004
  • [38] QUANTITATIVE XSPECT/CT: REDEFINING THE DIAGNOSIS OF TRANSTHYRETIN CARDIAC AMYLOIDOSIS
    Lindsay, K.
    Ramsay, S.
    INTERNAL MEDICINE JOURNAL, 2018, 48 : 7 - 8
  • [39] Expert Consensus Recommendations for the Suspicion and Diagnosis of Transthyretin Cardiac Amyloidosis
    Maurer, Mathew S.
    Bokhari, Sabahat
    Damy, Thibaud
    Dorbala, Sharmila
    Drachman, Brian M.
    Fontana, Marianna
    Grogan, Martha
    Kristen, Arnt V.
    Lousada, Isabelle
    Nativi-Nicolau, Jose
    Cristina Quarta, Candida
    Rapezzi, Claudio
    Ruberg, Frederick L.
    Witteles, Ronald
    Merlini, Giampaolo
    CIRCULATION-HEART FAILURE, 2019, 12 (09)
  • [40] Incidence and predictors of transthyretin cardiac amyloidosis in patients with degenerative aortic stenosis
    Abadie, B.
    Held, M.
    Puri, R.
    Krishnaswamy, A.
    Yun, J.
    Hanna, M.
    Reed, G.
    Kapadia, S.
    Jaber, W.
    EUROPEAN HEART JOURNAL, 2022, 43 : 1619 - 1619