Absence of mitochondrial progesterone receptor polymorphisms in women with spontaneous preterm birth

Tracy A. Manuck, Thomas M. Price, Elizabeth Thom, Paul J. Meis, Mitchell P. Dombrowski, Baha Sibai, Catherine Y. Spong, Dwight J. Rouse, Jay D. Iams, Hyagriv N. Simhan, Mary J. O'Sullivan, Menachem Miodovnik, Kenneth J. Leveno, Deborah Conway, Ronald J. Wapner, Marshall Carpenter, Brian Mercer, Susan M. Ramin, John M. Thorp, Alan M. Peaceman

Resultado de la investigación: Articlerevisión exhaustiva

4 Citas (Scopus)

Resumen

Objective: The truncated mitochondrial progesterone receptor (PR-M) is homologous to nuclear PRs with the exception of an amino terminus hydrophobic membrane localization sequence, which localizes PR-M to mitochondria. Given the matrilineal inheritance of both spontaneous preterm birth (SPTB) and the mitochondrial genome, we hypothesized that (a) PR-M is polymorphic and (b) PR-M localization sequence polymorphisms could result in variable progesterone-mitochondrial effects and variable responsiveness to progesterone prophylaxis. Methods: Secondary analysis of DNA from women enrolled in a multicenter, prospective, study of 17 alpha-hydroxyprogesterone caproate (17OHPC) versus placebo for the prevention of recurrent SPTB. DNA was extracted from stored saliva. Results: The PR-M localization sequence was sequenced on 344 patients. Sequences were compared with the previously published 48 base-pair sequence, and all were identical. Conclusions: We did not detect genetic variation in the mitochondrial localization sequence of the truncated PR-M in a group of women at high risk for SPTB.

Idioma originalEnglish (US)
Páginas (desde-hasta)913-916
Número de páginas4
PublicaciónReproductive Sciences
Volumen17
N.º10
DOI
EstadoPublished - oct. 2010
Publicado de forma externa

ASJC Scopus subject areas

  • Obstetrics and Gynecology

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