Rare Variant Mutations in Pregnancy-Associated or Peripartum Cardiomyopathy
Author(s) -
Ana Morales,
Thomas Painter,
Ran Li,
Jill D. Siegfried,
Duanxiang Li,
Nadine Norton,
Ray E. Hershberger
Publication year - 2010
Publication title -
circulation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.795
H-Index - 607
eISSN - 1524-4539
pISSN - 0009-7322
DOI - 10.1161/circulationaha.109.931220
Subject(s) - peripartum cardiomyopathy , medicine , dilated cardiomyopathy , pregnancy , pedigree chart , cardiomyopathy , mutation , myh7 , genetics , gene , heart failure , biology , gene isoform
The term peripartum cardiomyopathy (PPCM) describes dilated cardiomyopathy (DCM) without known cause that occurs during the last month of pregnancy to 5 months postpartum. A related term, pregnancy-associated cardiomyopathy (PACM), refers to DCM onset earlier in pregnancy. Multiple studies have focused on inflammatory, immunologic, and environmental causes. An alternative hypothesis is that PPCM and PACM result, in part, from a genetic cause. In this study, we sought to test the hypothesis that rare DCM-associated mutations underlie a proportion of PACM or PPCM cases.
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