Left ventricular dysfunction in ADPKD and effects of octreotide-LAR: A cross-sectional and longitudinal substudy of
Letizia Spinelli1, Antonio Pisani2, Giuseppe Giugliano1
1Department of Advanced Medical Sciences, Federico II University, Naples, Italy.
Insights
Autosomal dominant polycystic kidney disease (ADPKD) patients show early left ventricular (LV) dysfunction. Somatostatin-analogue octreotide-LAR treatment improved LV untwisting rate, suggesting potential for preventing cardiac issues in ADPKD.
Area of Science:
- Cardiology
- Nephrology
- Pharmacology
Background:
- Cardiac abnormalities, specifically left ventricular (LV) dysfunction, are observed in autosomal dominant polycystic kidney disease (ADPKD) patients prior to hypertension or renal impairment.
- Early detection and characterization of LV function in ADPKD are crucial for understanding disease progression and potential interventions.
Purpose of the Study:
- To assess LV function in ADPKD patients using speckle-tracking echocardiography.
- To evaluate the impact of somatostatin-analogue octreotide-LAR treatment on LV function in ADPKD patients.
Main Methods:
- A cross-sectional study compared LV function (twist and untwisting rates) in 34 ADPKD patients, 34 healthy controls, and 34 renal controls using speckle-tracking echocardiography.
- Changes in LV function were analyzed in ADPKD patients treated with octreotide-LAR or placebo over 3 years.
Main Results:
- ADPKD patients exhibited significantly lower LV twist and untwisting rates compared to both healthy and renal controls (p < 0.001).
- LV untwisting rate positively correlated with LV mass and diastolic blood pressure in ADPKD patients.
- Octreotide-LAR treatment significantly improved LV untwisting rate (p=0.027), with no change observed in the placebo group. Octreotide-LAR was the sole independent predictor of this improvement.
Conclusions:
- Left ventricular function is impaired early in the course of ADPKD.
- Somatostatin-analogue therapy, such as octreotide-LAR, shows promise in preventing or ameliorating LV dysfunction in ADPKD patients.
Background And Aim:
In autosomal dominant polycystic kidney disease (ADPKD) cardiac abnormalities have been observed before the onset of hypertension or renal dysfunction. We sought to characterize, in ADPKD patients, left ventricular (LV) function and its changes after somatostatin-analogue octreotide-LAR treatment.
Methods:
In a 1:1:1 cross-sectional study, we evaluated LV function by speckle-tracking echocardiography in 34 ADPKD patients from one ALADIN-trial center and in 34 age- and gender-matched healthy controls and 34 equally-matched renal controls with non-cystic chronic kidney disease. Changes in LV function were compared in the 16 and 18 ADPKD patients originally randomized to 3 year-treatment with octreotide-LAR or placebo, respectively.
Results:
LV twist and untwisting rates were lower in ADPKD patients that in healthy or renal controls (6.1 ± 2.6° vs. 11.1 ± 2.1° and 10.2 ± 3.7°; -49.5 ± 18.1°/s vs. -79.8 ± 12.2°/s and -84.3 ± 25.9°/s, respectively, all p < 0.001). The correlation between LV mass or diastolic BP and untwisting rate was positive in ADPKD patients (r = 0.38, p = 0.025 and r = 0.44, p = 0.011, respectively), not significant in healthy controls and negative in renal controls (r = -0.38; p = 0.023 and r = -0.40, p = 0.012, respectively. LV untwisting rate improved from -49.9 ± 18.6°/s to -70.3 ± 27.5°/s with octreotide-LAR, but did not change with placebo (p = 0.027 for treatment effect). At adjusted linear regression analysis, octreotide-LAR therapy emerged as the only independent predictor of untwisting rate improvement at final visit [beta coefficient -0.504 (95% CI -46.905--6.367), p = 0.014].
Conclusions:
In ADPKD patients LV function is early impaired. Somatostatin-analogue therapy might help in preventing or ameliorating LV dysfunction in this population. Clinical Trial Registration http://www.clinicaltrials.gov, NCT0030928.
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