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. 2008 Apr;93(4):1276-84.
doi: 10.1210/jc.2007-0425. Epub 2008 Jan 8.

Postmenopausal women with a history of irregular menses and elevated androgen measurements at high risk for worsening cardiovascular event-free survival: results from the National Institutes of Health--National Heart, Lung, and Blood Institute sponsored Women's Ischemia Syndrome Evaluation

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Postmenopausal women with a history of irregular menses and elevated androgen measurements at high risk for worsening cardiovascular event-free survival: results from the National Institutes of Health--National Heart, Lung, and Blood Institute sponsored Women's Ischemia Syndrome Evaluation

Leslee J Shaw et al. J Clin Endocrinol Metab. 2008 Apr.

Retraction in

  • Withdrawn by author.
    [No authors listed] [No authors listed] J Clin Endocrinol Metab. 2015 Mar;100(3):1206. doi: 10.1210/jc.2014-4415. J Clin Endocrinol Metab. 2015. PMID: 25701302 Free PMC article. No abstract available.

Abstract

Background: Women with polycystic ovary syndrome (PCOS) have a greater clustering of cardiac risk factors. However, the link between PCOS and cardiovascular (CV) disease is incompletely described.

Objective: The aim of this analysis was to evaluate the risk of CV events in 390 postmenopausal women enrolled in the National Institutes of Health-National Heart, Lung, and Blood Institute (NIH-NHLBI) sponsored Women's Ischemia Syndrome Evaluation (WISE) study according to clinical features of PCOS.

Methods: A total of 104 women had clinical features of PCOS defined by a premenopausal history of irregular menses and current biochemical evidence of hyperandrogenemia. Hyperandrogenemia was defined as the top quartile of androstenedione (> or = 701 pg/ml), testosterone (> or = 30.9 ng/dl), or free testosterone (> or = 4.5 pg/ml). Cox proportional hazard model was fit to estimate CV death or myocardial infarction (n = 55).

Results: Women with clinical features of PCOS were more often diabetic (P < 0.0001), obese (P = 0.005), had the metabolic syndrome (P < 0.0001), and had more angiographic coronary artery disease (CAD) (P = 0.04) compared to women without clinical features of PCOS. Cumulative 5-yr CV event-free survival was 78.9% for women with clinical features of PCOS (n = 104) vs. 88.7% for women without clinical features of PCOS (n = 286) (P = 0.006). PCOS remained a significant predictor (P < 0.01) in prognostic models including diabetes, waist circumference, hypertension, and angiographic CAD as covariates.

Conclusion: Among postmenopausal women evaluated for suspected ischemia, clinical features of PCOS are associated with more angiographic CAD and worsening CV event-free survival. Identification of postmenopausal women with clinical features of PCOS may provide an opportunity for risk factor intervention for the prevention of CAD and CV events.

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Figures

Figure 1
Figure 1
Average Hs-CRP values (95% CI) for women with and without clinical features of PCOS. Hs-CRP data were available in 278 of the 390 postmenopausal women.
Figure 2
Figure 2
Predicted CV event rates by quartile of free testosterone ranging from 8.0 to 15.1% for levels from no more than 1.8 to at least 4.5 pg/ml (P = 0.03).
Figure 3
Figure 3
Cumulative unadjusted CV death or MI free survival in postmenopausal women with or without clinical features of PCOS (P = 0.006).

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