Human induced pluripotent stem cells to unravel the pathophysiology of peripartum cardiomyopathy
- Conditions
- 10019280Peripartum cardiomyopathypregnancy-related heart failure
- Registration Number
- NL-OMON40927
- Lead Sponsor
- niversitair Medisch Centrum Groningen
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 24
Patients:
• Ages from 18 and older.
• Diagnosis PPCM according to the revised European Society of Cardiology guidelines 2012.
• Participation of healthy sister (or female cousin) that has been pregnant at least once without diagnosis of PPCM.
• Possibility of adequate communication.
• Informed consent is obtained.;Controls:
• Ages from 18 and older.
• Sister or (female) first cousin of patient.
• Generally in good health.
• Has been pregnant without cardiac complications.
• Possibility of adequate communication.
• Informed consent is obtained.
Patients:
• Other etiology of heart failure other than PPCM.
• A healthy sister (or female cousin) cannot be included, for any reason.
• Severe complications during pregnancy (aside from PPCM).
• Extensive skin disorder precluding a biopsy from unaffected skin area.
• Known allergy for local anesthetics.
• Informed consent can, for whatever reason, not be obtained.;Controls:
• Has never been pregnant.
• Severe complications during pregnancy (including cardiac complications)
• Extensive skin disorder precluding a biopsy from unaffected skin area.
• Known allergy for local anesthetics.
• Informed consent can, for whatever reason, not be obtained.
Study & Design
- Study Type
- Observational invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method <p>- IPS cells can be generated from skin fibroblasts of test subjects and can be<br /><br>differentiated into cardiomyocytes.<br /><br>- Cardiomyocytes derived from test subjects via IPS reprogramming show<br /><br>differences in expression profiles and in responses to stress in comparison to<br /><br>those of healthy controls.</p><br>
- Secondary Outcome Measures
Name Time Method <p>Not applicable</p><br>