Cardiac (CMRI) Assessment of Acromegaly
- Registration Number
- NCT02948322
- Lead Sponsor
- Assistance Publique - Hôpitaux de Paris
- Brief Summary
In this study, the investigators will evaluate the cardiac structure and function, focusing on the myocardial water content and interstitial fibrosis, in patients with active acromegaly in comparison with 1) healthy volunteers, 2) the same acromegalic patients that have received efficient therapy.
The investigators hypothesize that the myocardial water content in acromegaly is increased as these patients present with sodium and water retention and that this myocardial water infiltration will improve with efficient treatment of the disease. They will thus assess using CMRI, this parameter by measuring the myocardial transverse relaxation time (T2), reflecting water content in the myocardium.
- Detailed Description
Patients with acromegaly have left ventricular (LV) hypertrophy and dysfunction on echocardiography, but only very few studies have been performed using cardiac magnetic resonance imaging (CMRI), currently the reference modality is assessment in cardiac geometry function. In addition, no data are available on right ventricular (RV) and atrial structure and function. The pathophysiology of the cardiac involvement in acromegaly may be related to increase myocardiac water content and/or interstitial myocardiac fibrosis.
The main objective of sthe study is to compare the myocardial water content in patients with acromegaly and in healthy volunteers. Secondary objectives of the study are to evaluate :
1. interstitial fibrosis and the structure and the function of LV and RV in acromegalic patients in comparison with healthy volunteers;
2. the reversibility of the cardiac involvement (water content, fibrosis, LV and RV structure and function) after efficient treatment of acromegaly;
3. the elasticity of aorta in acromegalic patients in comparison with healthy volunteers and with the post-treatment state. Twenty acromegalic patients will be included in order to dispose of 15 patients that will completed the study and the same number of age- and BMI-adjusted healthy volunteers will be included.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 28
- Active acromegaly as defined by the usual diagnostic criteria (de novo patients or patients uncontrolled by previous treatments).
- Healthy volunteers matched for age, sex and BMI with the patients of the group 1
- History of coronary heart disease (acute or chronic myocardial ischemia)
- Acute or chronic renal failure (creatinin clearance 30 mL/min/l,73m2)
- Contraindication of MRI
- Hypersensitivity to gadolinium
- Pregnancy
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description OGTT, CMRI with gadolinium in patients CMRI Patients with acromegaly will be investigated OGTT, CMRI with gadolinium in volunteers OGTT Age-, sex- and BMI-matched healthy volunteers will be investigated OGTT, CMRI with gadolinium in volunteers CMRI Age-, sex- and BMI-matched healthy volunteers will be investigated OGTT, CMRI with gadolinium in patients OGTT Patients with acromegaly will be investigated OGTT, CMRI with gadolinium in patients Gadolinium Patients with acromegaly will be investigated OGTT, CMRI with gadolinium in volunteers Gadolinium Age-, sex- and BMI-matched healthy volunteers will be investigated
- Primary Outcome Measures
Name Time Method Myocardial transverse relaxation time (T2), reflecting water content assessed by CMRI Baseline in acromegalic patients; at the 1 day evaluation visit in healthy volunteers This outcome will be compared between patients and healthy volunteers.
Change from baseline Myocardial transverse relaxation time (T2) at 6 months, reflecting water content assessed by CMRI Baseline and 6 months after beginning of the treatment in acromegalic patients
- Secondary Outcome Measures
Name Time Method Function including Left Auricular ejection fractions will also be assessed CMRI Baseline in acromegalic patients; at the 1 day evaluation visit in healthy volunteers Interstitial myocardial fibrosis Baseline in acromegalic patients; at the 1 day evaluation visit in healthy volunteers Interstitial myocardial fibrosis will be quantified by T1 measurements before and after gadolinium injection.
Function including Right Ventricular ejection fractions will also be assessed CMRI Baseline in acromegalic patients; at the 1 day evaluation visit in healthy volunteers Dense myocardial fibrosis Baseline in acromegalic patients; at the 1 day evaluation visit in healthy volunteers The dense myocardial fibrosis will be depicted by late gadolinium enhancement.
Function including Left Ventricular ejection fractions will also be assessed CMRI Baseline in acromegalic patients; at the 1 day evaluation visit in healthy volunteers Function including Left Ventricular and Right Ventricular stroke volumes will also be assessed CMRI Baseline in acromegalic patients; at the 1 day evaluation visit in healthy volunteers Cardiac morphology will also be assessed CMRI Baseline in acromegalic patients; at the 1 day evaluation visit in healthy volunteers Function including Left Ventricular mass index will also be assessed CMRI Baseline in acromegalic patients; at the 1 day evaluation visit in healthy volunteers Change from baseline interstitial myocardial fibrosis at 6 months Baseline and 6 months after beginning of the treatment in acromegalic patients Change from baseline Dense myocardial fibrosis at 6 months Baseline and 6 months after beginning of the treatment in acromegalic patients "The dense myocardial fibrosis will be depicted by late gadolinium enhancement.
Trial Locations
- Locations (1)
AP-HP, Bicêtre Hospital
🇫🇷Le Kremlin Bicêtre, France