TY - JOUR
T1 - Endothelial function measured using flow-mediated dilation in polycystic ovary syndrome
T2 - A meta-analysis of the observational studies
AU - Sprung, Victoria S.
AU - Atkinson, Greg
AU - Cuthbertson, Daniel J.
AU - Pugh, Christopher J.A.
AU - Aziz, Nabil
AU - Green, Daniel J.
AU - Cable, N. Timothy
AU - Jones, Helen
PY - 2012/7/9
Y1 - 2012/7/9
N2 - Objective Women with polycystic ovary syndrome (PCOS) demonstrate an increased prevalence of cardiovascular disease (CVD) risk factors. Previous researchers have compared flow-mediated dilation (FMD), an early marker of CVD, in women with and without PCOS. Evidence for a PCOS-mediated reduction in FMD remains equivocal, potentially because of study differences in cohort-matching and measurement approaches. The aims of this systematic review and meta-analysis were to examine to what extent FMD is impaired in PCOS and to explore the influence of potential moderators of FMD reduction, such as age and BMI. Design A systematic review and meta-analysis of published observational studies comparing FMD in PCOS with control women. Patients Twenty-one published studies were included (PCOS, n = 908; controls, n = 566). A subanalysis, using tighter inclusion criteria, involved seven studies (PCOS, n = 402; control, n = 251). Measurements Mean differences in FMD between PCOS and controls were synthesized. The subanalysis was delimited to the inclusion of age and BMI-matched controls. These factors were then explored as moderators using meta-regression. Results The pooled mean FMD was 3·4% (95% CI=1·9, 4·9) lower in PCOS compared with control women, with substantial heterogeneity between studies. In the subanalysis, the PCOS-mediated reduction in FMD was 4·1% (95% CI=2·7, 5·5). Heterogeneity remained substantial (I 2=81%). Subsequent meta-regression indicated that the magnitude of FMD difference was not influenced by BMI (P = 0·17) nor age (P = 0·38). Conclusions This systematic research synthesis indicates that endothelial function is compromised in PCOS women, even if they are young and nonobese.
AB - Objective Women with polycystic ovary syndrome (PCOS) demonstrate an increased prevalence of cardiovascular disease (CVD) risk factors. Previous researchers have compared flow-mediated dilation (FMD), an early marker of CVD, in women with and without PCOS. Evidence for a PCOS-mediated reduction in FMD remains equivocal, potentially because of study differences in cohort-matching and measurement approaches. The aims of this systematic review and meta-analysis were to examine to what extent FMD is impaired in PCOS and to explore the influence of potential moderators of FMD reduction, such as age and BMI. Design A systematic review and meta-analysis of published observational studies comparing FMD in PCOS with control women. Patients Twenty-one published studies were included (PCOS, n = 908; controls, n = 566). A subanalysis, using tighter inclusion criteria, involved seven studies (PCOS, n = 402; control, n = 251). Measurements Mean differences in FMD between PCOS and controls were synthesized. The subanalysis was delimited to the inclusion of age and BMI-matched controls. These factors were then explored as moderators using meta-regression. Results The pooled mean FMD was 3·4% (95% CI=1·9, 4·9) lower in PCOS compared with control women, with substantial heterogeneity between studies. In the subanalysis, the PCOS-mediated reduction in FMD was 4·1% (95% CI=2·7, 5·5). Heterogeneity remained substantial (I 2=81%). Subsequent meta-regression indicated that the magnitude of FMD difference was not influenced by BMI (P = 0·17) nor age (P = 0·38). Conclusions This systematic research synthesis indicates that endothelial function is compromised in PCOS women, even if they are young and nonobese.
UR - http://www.scopus.com/inward/record.url?scp=84872940533&partnerID=8YFLogxK
U2 - 10.1111/j.1365-2265.2012.04490.x
DO - 10.1111/j.1365-2265.2012.04490.x
M3 - Article
C2 - 22775449
AN - SCOPUS:84872940533
SN - 0300-0664
VL - 78
SP - 438
EP - 446
JO - Clinical Endocrinology
JF - Clinical Endocrinology
IS - 3
ER -