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      Age at Menarche and Risk of Cardiovascular Disease Outcomes: Findings From the National Heart Lung and Blood Institute‐Sponsored Women's Ischemia Syndrome Evaluation

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          Abstract

          Background

          Previous studies have reported an association between the timing of menarche and cardiovascular disease ( CVD). However, emerging studies have not examined the timing of menarche in relation to role of estrogen over a lifetime and major adverse cardiac events ( MACE).

          Methods and Results

          A total of 648 women without surgical menopause undergoing coronary angiography for suspected ischemia in the WISE (Women's Ischemia Syndrome Evaluation) study were evaluated at baseline and followed for 6 years (median) to assess major adverse CVD outcomes. MACE was defined as the first occurrence of all‐cause death, nonfatal myocardial infarction, nonfatal stroke, or heart failure hospitalization. Age at menarche was self‐reported and categorized (≤10, 11, 12, 13, 14, ≥15 years) with age 12 as reference. Total estrogen time and supra–total estrogen time were calculated. Cox regression analysis was performed adjusting for CVD risk factors. Baseline age was 57.9 ± 12 years (mean ± SD), body mass index was 29.5 ± 6.5 kg/m 2, total estrogen time was 32.2 ± 8.9 years, and supra–total estrogen time was 41.4 ± 8.8 years. MACE occurred in 172 (27%), and its adjusted regression model was J‐shaped. Compared with women with menarche at age 12 years, the adjusted MACE hazard ratio for menarche at ≤10 years was 4.53 (95% CI 2.13‐9.63); and at ≥15 years risk for MACE was 2.58 (95% CI, 1.28‐5.21).

          Conclusions

          History of early or late menarche was associated with a higher risk for adverse CVD outcomes. These findings highlight age at menarche as a potential screening tool for women at risk of adverse CVD events.

          Clinical Trial Registration

          URL: http://www.clinicaltrials.gov. Unique identifier: NCT00000554.

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          Most cited references23

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          Insights from the NHLBI-Sponsored Women's Ischemia Syndrome Evaluation (WISE) Study: Part II: gender differences in presentation, diagnosis, and outcome with regard to gender-based pathophysiology of atherosclerosis and macrovascular and microvascular coronary disease.

          Coronary heart disease is the leading cause of death and disability in the U.S., but recent advances have not led to declines in case fatality rates for women. The current review highlights gender-specific issues in ischemic heart disease (IHD) presentation, evaluation, and outcomes with a special focus on the results derived from the National Institutes of Health-National Heart, Lung, and Blood Institute-sponsored Women's Ischemia Syndrome Evaluation (WISE) study. In the second part of this review, we will assess new evidence on gender-based differences in vascular wall or metabolic alterations, atherosclerotic plaque deposition, and functional expression on worsening outcomes of women. Additionally, innovative cardiovascular imaging techniques will be discussed. Finally, we identify critical areas of further inquiry needed to advance this new gender-specific IHD understanding into improved outcomes for women.
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            Early age at menarche associated with cardiovascular disease and mortality.

            The relationship between age at menarche and cardiovascular disease remains unclear. Two recent studies found an inverse association between age at menarche and all-cause mortality. The aim of this study was to examine the relationship between age at menarche and cardiovascular disease risk factors, events, and mortality. A population-based prospective study involving 15,807 women, aged 40-79 yr in 1993-1997 and followed up to March 2007 for cardiovascular disease events (median follow-up 10.6 yr) and February 2008 for mortality (median follow-up 12.0 yr) was used. Odds ratios for cardiovascular disease risk factors and hazard ratios for incident cardiovascular disease and mortality were calculated. There were 3888 incident cardiovascular disease events (1323 coronary heart disease, 602 stroke, and 1963 other) and 1903 deaths (640 cardiovascular disease, 782 cancer, and 481 other) during follow-up. Compared with other women, those who had early menarche (<12 yr) had higher risks of hypertension [1.13 (1.02-1.24)], incident cardiovascular disease [1.17 (1.07-1.27)], incident coronary heart disease [1.23 (1.06-1.43)], all-cause mortality [1.22 (1.07-1.39)], cardiovascular disease mortality [1.28 (1.02-1.62)], and cancer mortality [1.25 (1.03-1.51)], adjusted for age, physical activity, smoking, alcohol, educational level, occupational social class, oral contraceptive use, hormone replacement therapy, parity, body mass index, and waist circumference. Early age at menarche (before age 12 yr) was associated with increased risk of cardiovascular disease events, cardiovascular disease mortality, and overall mortality in women, and this association appeared to be only partly mediated by increased adiposity.
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              Coronary microvascular dysfunction is highly prevalent in women with chest pain in the absence of coronary artery disease: results from the NHLBI WISE study.

              Chest pain in the absence of obstructive coronary artery disease (CAD) is common in women; it is frequently associated with debilitating symptoms and repeated evaluations and may be caused by coronary microvascular dysfunction. However, the prevalence and determinants of microvascular dysfunction in these women are uncertain. We measured coronary flow velocity reserve (coronary velocity response to intracoronary adenosine) to evaluate the coronary microvasculature and risk factors for atherosclerosis in 159 women (mean age, 52.9 years) with chest pain and no obstructive CAD. All women were referred for coronary angiography to evaluate their chest pain as part of the Women's Ischemia Syndrome Evaluation (WISE) study. Seventy-four (47%) women had subnormal (<2.5) coronary flow velocity reserve suggestive of microvascular dysfunction (mean, 2.02 +/- 0.38); 85 (53%) had normal reserve (mean, 3.13 +/- 0.64). Demographic characteristics, blood pressure, ventricular function, lipid levels, and reproductive hormone levels were not significantly different between women with normal and those with abnormal microvascular function. Postmenopausal hormone use within 3 months was significantly less prevalent among those with microvascular dysfunction (40% vs 60%, P =.032). Age and number of years past menopause correlated with flow velocity reserve (r = -0.18, P =.02, and r = -0.30, P <.001, respectively). No significant associations were identified between flow velocity reserve and lipid and hormone levels, blood pressure, and left ventricular ejection fraction. Coronary microvascular dysfunction is present in approximately one half of women with chest pain in the absence of obstructive CAD and cannot be predicted by risk factors for atherosclerosis and hormone levels. Therefore, the diagnosis of coronary microvascular dysfunction should be considered in women with chest pain not attributable to obstructive CAD.
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                Author and article information

                Contributors
                noel.baireymerz@cshs.org
                Journal
                J Am Heart Assoc
                J Am Heart Assoc
                10.1002/(ISSN)2047-9980
                JAH3
                ahaoa
                Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease
                John Wiley and Sons Inc. (Hoboken )
                2047-9980
                05 June 2019
                18 June 2019
                : 8
                : 12 ( doiID: 10.1002/jah3.2019.8.issue-12 )
                : e012406
                Affiliations
                [ 1 ] Jacobs School of Medicine and Biomedical Sciences University at Buffalo NY
                [ 2 ] Biostatistics & Bioinformatics Center Cedars‐Sinai Medical Center Los Angeles CA
                [ 3 ] Department of Medicine Cedars‐Sinai Medical Center Los Angeles CA
                [ 4 ] Department of Epidemiology University of Pittsburgh Graduate School of Public Health Pittsburgh PA
                [ 5 ] Division of Reproductive Endocrinology and Infertility Department of Obstetrics and Gynecology University of Utah Salt Lake City UT
                [ 6 ] Department of Obstetrics and Gynecology Keck School of Medicine of University of Southern California Los Angeles CA
                [ 7 ] Division of Cardiology Department of Medicine University of Florida Gainesville FL
                [ 8 ] Barbra Streisand Women's Heart Center Cedars‐Sinai Smidt Heart Institute Los Angeles CA
                Author notes
                [*] [* ] Correspondence to: C. Noel Bairey Merz, MD, FAHA, FACC, 127 S San Vicente Blvd, Suite A3206, Los Angeles, CA 90048. E‐mail: noel.baireymerz@ 123456cshs.org
                Article
                JAH34177
                10.1161/JAHA.119.012406
                6645646
                31165670
                a91566c9-d990-4224-adae-5e15e72b69ce
                © 2019 The Authors. Published on behalf of the American Heart Association, Inc., by Wiley.

                This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.

                History
                : 26 February 2019
                : 03 May 2019
                Page count
                Figures: 2, Tables: 2, Pages: 9, Words: 6609
                Funding
                Funded by: National Heart, Lung, and Blood Institute
                Award ID: N01‐HV‐68161
                Award ID: N01‐HV‐68162
                Award ID: N01‐HV‐68163
                Award ID: N01‐HV‐68164
                Award ID: K23‐HL127262‐01A1
                Award ID: K23‐HL125941‐01A1
                Funded by: National Institute on Aging
                Award ID: U0164829
                Award ID: U01 HL649141
                Award ID: U01 HL649241
                Award ID: K23HL105787
                Award ID: T32HL69751
                Award ID: R01 HL090957
                Award ID: 1R03AG032631
                Funded by: National Center for Research Resources
                Award ID: MO1‐RR00425
                Funded by: National Center for Advancing Translational Sciences
                Award ID: UL1TR000124
                Award ID: UL1TR000064
                Funded by: Gustavus and Louis Pfeiffer Research Foundation
                Funded by: The Women's Guild of Cedars‐Sinai Medical Center
                Funded by: The Ladies Hospital Aid Society of Western Pennsylvania
                Funded by: QMED, Inc
                Funded by: Cedars‐Sinai Medical Center
                Funded by: Society for Women's Health Research
                Funded by: Linda Joy Pollin Women's Heart Health Program
                Categories
                Original Research
                Original Research
                Epidemiology
                Custom metadata
                2.0
                jah34177
                18 June 2019
                Converter:WILEY_ML3GV2_TO_NLMPMC version:5.6.4 mode:remove_FC converted:18.06.2019

                Cardiovascular Medicine
                cardiovascular disease outcomes,estrogen,menarche,risk factors,women,cardiovascular disease

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