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Longitudinal Assessment of Left Ventricular Mass in Autosomal Dominant Polycystic Kidney Disease.
Dad, Taimur; Abebe, Kaleab Z; Bae, K Ty; Comer, Diane; Torres, Vicente E; Czarnecki, Peter G; Schrier, Robert W; Steinman, Theodore I; Moore, Charity G; Chapman, Arlene B; Kaya, Diana; Tao, Cheng; Braun, William E; Winklhofer, Franz T; Brosnahan, Godela; Hogan, Marie C; Miskulin, Dana C; Rahbari Oskoui, Frederic; Flessner, Michael F; Perrone, Ronald D.
Afiliación
  • Dad T; Division of Nephrology, Department of Medicine, Tufts Medical Center, Boston, Massachusetts, USA.
  • Abebe KZ; Department of Medicine, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, USA.
  • Bae KT; Department of Radiology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, USA.
  • Comer D; Department of Medicine, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, USA.
  • Torres VE; Division of Nephrology and Hypertension, Mayo Clinic, Rochester, Minnesota, USA.
  • Czarnecki PG; Division of Renal Medicine, Brigham and Women's Hospital, Boston, Massachusetts, USA.
  • Schrier RW; Department of Medicine, University of Colorado Health Sciences Center, Denver, Colorado, USA.
  • Steinman TI; Department of Medicine, Beth Israel Deaconess Medical Center, Boston, Massachusetts, USA.
  • Moore CG; Department of Medicine, Brigham and Womens' Hospital, Boston, Massachusetts, USA.
  • Chapman AB; Department of Physical Therapy, University of Pittsburgh, Pittsburgh, PA.
  • Kaya D; Department of Medicine, Biological Sciences Department, University of Chicago, Chicago, Illinois, USA.
  • Tao C; Department of Oncologic Neuroradiology, University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
  • Braun WE; Department of Radiation Oncology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, USA.
  • Winklhofer FT; Department of Nephrology, Cleveland Clinic, Cleveland, Ohio, USA.
  • Brosnahan G; Division of Nephrology, Department of Internal Medicine, Kansas University Medical Center, Kansas City, Kansas, USA.
  • Hogan MC; Department of Medicine, University of Colorado Health Sciences Center, Denver, Colorado, USA.
  • Miskulin DC; Division of Nephrology, Department of Internal Medicine, Mayo Clinic, Rochester, Minnesota, USA.
  • Rahbari Oskoui F; Division of Nephrology, Department of Medicine, Tufts Medical Center, Boston, Massachusetts, USA.
  • Flessner MF; Department of Medicine, Renal Division, Emory University School of Medicine, Atlanta, Georgia, USA.
  • Perrone RD; National Institutes of Health (NIDDK), Bethesda, Maryland, USA.
Kidney Int Rep ; 3(3): 619-624, 2018 May.
Article en En | MEDLINE | ID: mdl-29854969
ABSTRACT

INTRODUCTION:

The high burden of cardiovascular morbidity and mortality in autosomal dominant polycystic kidney disease (ADPKD) is related to development of hypertension and left ventricular hypertrophy. Blood pressure reduction has been shown to reduce left ventricular mass in ADPKD; however, moderators and predictors of response to lower blood pressure are unknown.

METHODS:

This was a post hoc cohort analysis of HALT PKD study A, a randomized placebo controlled trial examining the effect of low blood pressure and single versus dual renin-angiotensin blockade in early ADPKD. Participants were hypertensive ADPKD patients 15 to 49 years of age with estimated glomerular filtration rate (eGFR) > 60 ml/min per 1.73 m2 across 7 centers in the United States. Predictors included age, sex, baseline eGFR, systolic blood pressure, total kidney volume, serum potassium, and urine sodium, potassium, albumin, and aldosterone. Outcome was left ventricular mass index (LVMI) measured using 1.5-T magnetic resonance imaging at months 0, 24, 48, and 60.

RESULTS:

Reduction in LVMI was associated with higher baseline systolic blood pressure and larger kidney volume regardless of blood pressure control group assignment (P < 0.001 for both). Male sex and baseline eGFR were associated with a positive annual slope in LVMI (P < 0.001 and P = 0.07, respectively).

CONCLUSION:

Characteristics associated with higher risk of progression in ADPKD, including higher systolic blood pressure, larger kidney volume, and lower eGFR are associated with improvement in LVMI with intensive blood pressure control, whereas male sex is associated with a smaller slope of reduction in LVMI.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Clinical_trials / Observational_studies / Prognostic_studies / Risk_factors_studies Idioma: En Revista: Kidney Int Rep Año: 2018 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Clinical_trials / Observational_studies / Prognostic_studies / Risk_factors_studies Idioma: En Revista: Kidney Int Rep Año: 2018 Tipo del documento: Article País de afiliación: Estados Unidos