Systematic Reviews
Disparities in cardio metabolic risk between Black and White women with polycystic ovary syndrome: a systematic review and meta-analysis

https://doi.org/10.1016/j.ajog.2020.12.019Get rights and content

Objective

We conducted a systematic review and meta-analysis to summarize and quantitatively pool evidence on cardiometabolic health disparities between Black and White women with polycystic ovary syndrome in the United States in response to the call for further delineation of these disparities in the international evidence-based guideline for the assessment and management of polycystic ovary syndrome.

Data Sources

Databases of MEDLINE, Web of Science, and Scopus were searched initially through March 05, 2020, and confirmed on September 11, 2020.

Study Eligibility Criteria

Observational studies documenting cardiometabolic risk profile (glucoregulatory, lipid profile, anthropometric, and blood pressure status) in Black and White women with polycystic ovary syndrome were included. Studies on children (<17 years old) and pregnant or menopausal-aged women (>50 years) were excluded. The primary outcome was fasting glucose. Furthermore, data on major cardiovascular events (stroke, coronary heart disease, heart failure) and mortality rate (cardiovascular death, total mortality) were evaluated.

Methods

Data were pooled by random-effects models and expressed as mean differences and 95% confidence intervals. Studies were weighted based on the inverse of the variance. Heterogeneity was evaluated by Cochran Q and I2 statistics. Study methodologic quality was assessed by the Newcastle-Ottawa scale.

Results

A total of 11 studies (N=2851 [652 Black and 2199 White]) evaluated cardiometabolic risk profile and all had high quality (Newcastle-Ottawa scale score of ≥8). No studies reported on cardiovascular events and mortality rate. Black women had comparable fasting glucose (−0.61 [−1.69 to 2.92] mg/dL; I2=62.5%), yet exhibited increased fasting insulin (6.76 [4.97–8.56] μIU/mL; I2=59.0%); homeostatic model assessment of insulin resistance (1.47 [0.86–2.08]; I2=83.2%); systolic blood pressure (3.32 [0.34–6.30] mm Hg; I2=52.0%); and decreased triglyceride (−32.56 [−54.69 to −10.42] mg/dL; I2=68.0%) compared with White women (all, P≤.03). Groups exhibited comparable total cholesterol, low-density lipoprotein cholesterol, high-density lipoprotein cholesterol, and diastolic blood pressure (all, P≥.06).

Conclusions

Black women with polycystic ovary syndrome have a greater tendency for an adverse cardiometabolic risk profile (increased insulin, homeostatic model assessment of insulin resistance, and systolic blood pressure) despite lower triglycerides than White women. Our observations support the consideration of these disparities for diagnostic, monitoring, and management practices in Black women and for future guideline recommendations. Given the heterogeneity among studies, future research should address the relative contributions of biologic, environmental, socioeconomic, and healthcare factors to the observed disparities. Furthermore, longitudinal research is required to address patient-pressing complications, including cardiovascular events and mortality rate in Black women with polycystic ovary syndrome as a high-risk yet understudied population.

Introduction

Women with polycystic ovary syndrome (PCOS) exhibit an adverse cardiometabolic risk profile compared with their counterparts without PCOS.1, 2, 3 Poor glucoregulatory status, characterized by abnormal glucose and insulin levels secondary to insulin resistance (IR), is the key pathophysiological factor associated with a wide range of metabolic disruptions in PCOS.2,4,5 Although the true risk of cardiovascular mortality remains unclear in this clinical population,6 the theoretical risk is substantial and warrants consideration of treatment and prevention strategies given both short- and long-term implications of cardiometabolic aberrations on pregnancy outcomes, lifelong health, and wellness.

AJOG at a Glance

We aimed to evaluate cardiometabolic health disparities between Black and White women with polycystic ovary syndrome (PCOS) in the United States.

Black women with PCOS have a greater tendency for adverse cardiometabolic risk profiles, evidenced by increased insulin, insulin resistance, and systolic blood pressure, despite lower triglyceride levels than White women.

This is the first systematic review to show a disproportionate cardiometabolic risk burden among Black women with PCOS in the United States. Our findings support the need to address health disparities in current clinical practice, future guideline development, and longitudinal research evaluating cardiovascular events and mortality rate in Black women with PCOS as a high-risk understudied population.

The degree to which cardiometabolic aberrations may disproportionately impact diverse populations of women with PCOS is important yet understudied. We and others have shown differences in cardiovascular risk factors, metabolic syndrome (MetS) rate, prediabetes, and type 2 diabetes status across diverse populations of women with PCOS in the United States and worldwide, supporting the potential for cardiometabolic health disparities in Indigenous, South Asian, Middle Eastern, and Black women compared with White or Caucasian counterparts.10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 7, 8, 9 The recent international evidence-based guideline for the assessment and management of PCOS emphasizes the need to further delineate these disparities to inform targeted diagnosis, monitoring, and management of high-risk clinical populations and subsequent adaptations of the guideline recommendations across geographic regions and clinical settings.26 Although the guideline recommends that health professionals consider presentation and manifestations of PCOS across diverse populations,26 our knowledge about the presence and magnitude of cardiometabolic health disparities is far from complete and remains to be elucidated.

In the United States, our knowledge about health disparities in the context of PCOS is limited to a few cross-sectional analyses that have yielded inconsistent results. Black or African Americans are a large underrepresented group in the United States. According to the Census Bureau (2019) data, approximately 44 million people in the United States are Black alone, representing 13.4% of the total population.27 However, Black women with PCOS are understudied, and their cardiometabolic characteristics have yielded conflicting results compared with their White counterparts. Some studies reported a worse cardiometabolic profile in Black compared with White women with PCOS, as evidenced by increased fasting glucose,14 increased fasting insulin,8,9,11,13, 14, 15,17,20 elevated systolic blood pressure (SBP)7,8,14 and diastolic blood pressure (DBP),7,14 decreased high-density lipoprotein cholesterol (HDL-C),7,14 and increased MetS rate.7,14 Conversely, others showed no differences between these groups in fasting glucose,7,9,11,13,16,17 fasting insulin,16,18,19 SBP,10,17, 18, 19, 20 DBP,10,17, 18, 19, 20 total cholesterol (TC),12,15,17 low-density lipoprotein cholesterol (LDL-C),8,17,19 HDL-C,8,10,12 waist circumference (WC),9,10,18 and waist to hip ratio.11,12 To complicate matters, there is even evidence to support that Black women with PCOS have a more favorable cardiometabolic profile than White women, as assessed by decreased TC,8,14 increased HDL-C,15,17 decreased LDL-C,12 and triglyceride (TG).7,10,12,14,15,17

The inconsistency may stem, in part, from the small sample sizes of individual studies, which have limited their statistical power to capture health disparities in cardiometabolic outcomes. Difficulties in establishing accurate PCOS status owing to reliance on self-reported diagnosis and unreliable measures of androgen status28 and ovarian morphology29, 30, 31 may have also contributed. The use of retrospective data and failure to account for variations in age, adiposity, lifestyle, and socioeconomic status across studies may have led to inconsistent findings. Furthermore, data regarding cardiovascular events (eg, nonfatal stroke, myocardial infarction, and heart failure), cardiovascular mortality, or total mortality are sparse in Black women with PCOS. Collectively, whether Black and White women with PCOS exhibit cardiometabolic risk differences remains unknown yet is critical for sustainable and successful management strategies that set the foundation for achieving health equity in this clinical population.32

To address this knowledge gap, we conducted a systematic review and meta-analysis to characterize cardiometabolic health disparities between Black and White women with PCOS in the United States. Our primary aim was to assess whether Black women with PCOS exhibited worse glucoregulatory status, as assessed by increased fasting glucose, than White women. As our secondary aim, we evaluated whether other cardiometabolic risk factors (glucoregulatory [insulin, IR], anthropometric, lipid profile, and blood pressure status), major cardiovascular events (stroke, coronary heart disease, and heart failure), and the mortality rate (cardiovascular death and total mortality) were exacerbated in Black women with PCOS than their White counterparts. Our focus on these cohorts is relevant because data from the general population have shown a substantial and persistent risk for cardiovascular disease and type 2 diabetes morbidity and or mortality in Black vs White cohorts,33,34 which could manifest early in reproductive-aged women with PCOS with underlying metabolic complications, warranting early preventative and management modalities. We hypothesized that Black women with PCOS would exhibit increased glucoregulatory dysregulation (increased glucose, IR, and hyperinsulinemia) and an overall worse cardiometabolic risk compared with White women with PCOS.

Section snippets

Methods

The work presented herein was performed according to the Preferred Reporting Items for Systematic Reviews and Meta-analyses guidelines.35 The study protocol is available at the International Prospective Register of Systematic Reviews (registration identification: CRD42020183485).

Literature search

The systematic search resulted in 3327 records (Figure 1), of which 11 studies7,8,10,11,14,15,17, 18, 19, 20 were eligible and included to evaluate cardiometabolic risk profile between Black and White women; however, we identified no studies that evaluated cardiovascular events or mortality rates. Selected studies comprised a total of 2851 participants, and 22 experimental arms (n=652 in the Black or African American [11 arms] and 2199 in the White or Caucasian [11 arms]) were included in the

Main findings

The present systematic review and meta-analysis of 11 studies, comprising 2851 reproductive-aged women who were predominantly obese living with PCOS in the United States, showed a tendency for a more adverse cardiometabolic risk profile in Black women with PCOS. Namely, Black women showed higher fasting insulin, HOMA-IR, and SBP, despite lower TG concentrations, than their White counterparts. Overall, these observations may highlight a disproportionate burden of PCOS within Black women in the

Acknowledgments

The authors gratefully acknowledge the enthusiastic support of librarians and statisticians at Cornell University who contributed to the methodology and conduct of the present study. We thank librarians Ms Kate Ghezzi-Kopel and Ms Kelly Johnson at Cornell University Library Evidence Synthesis Service for their contributions to the development of search strategy and implementation. We thank Ms Aprile Bertomo and Ms Gabriella Spinola at the Division of Nutritional Sciences at Cornell University

References (151)

  • M.C. Ernst et al.

    Chemerin: at the crossroads of inflammation and obesity

    Trends Endocrinol Metab

    (2010)
  • R.J. Chang et al.

    Diagnosis of polycystic ovary syndrome

    Endocrinol Metab Clin North Am

    (1999)
  • J.M. Conway et al.

    Visceral adipose tissue differences in black and white women

    Am J Clin Nutr

    (1995)
  • L. Palaniappan et al.

    Cardiovascular risk factors in ethnic minority women aged < or =30 years

    Am J Cardiol

    (2002)
  • T.E. Fuller-Rowell et al.

    Disparities in insulin resistance between Black and White adults in the United States: the role of lifespan stress exposure

    Psychoneuroendocrinology

    (2019)
  • A.C. Ellis et al.

    Ethnic differences in glucose disposal, hepatic insulin sensitivity, and endogenous glucose production among African American and European American women

    Metabolism

    (2012)
  • D.P. Schuster et al.

    Differential impact of obesity on glucose metabolism in Black and White American adolescents

    Am J Med Sci

    (1998)
  • A.E. Sumner et al.

    Ethnic differences in the ability of triglyceride levels to identify insulin resistance

    Atherosclerosis

    (2008)
  • I.S. Okosun et al.

    Abdominal adiposity and clustering of multiple metabolic syndrome in white, black and Hispanic Americans

    Ann Epidemiol

    (2000)
  • S.X. Lin et al.

    Racial/ethnic differences in the association of triglycerides with other metabolic syndrome components: the Multi-Ethnic Study of Atherosclerosis

    Metab Syndr Relat Disord

    (2011)
  • G.M.M. Hosain et al.

    Racial differences in the association between body fat distribution and lipid profiles among reproductive-age women

    Diabetes Metab

    (2010)
  • S.E. Walker et al.

    Racial/ethnic discrepancies in the metabolic syndrome begin in childhood and persist after adjustment for environmental factors

    Nutr Metab Cardiovasc Dis

    (2012)
  • N. Ellman et al.

    Ethnic differences in the association between lipid metabolism genes and lipid levels in black and white South African women

    Atherosclerosis

    (2015)
  • A.E. Sumner et al.

    Low HDL-cholesterol with normal triglyceride levels is the most common lipid pattern in West Africans and African Americans with metabolic syndrome: implications for cardiovascular disease prevention

    CVD Prev Control

    (2010)
  • A.R. Bentley et al.

    Interethnic differences in serum lipids and implications for cardiometabolic disease risk in African Ancestry populations

    Glob Heart

    (2017)
  • C.Y. Yoon et al.

    Insulin resistance is associated with new-onset cardiovascular events in nondiabetic patients undergoing peritoneal dialysis

    Kidney Res Clin Pract

    (2014)
  • C. Papandreou et al.

    Plasma metabolites predict both insulin resistance and incident type 2 diabetes: a metabolomics approach within the Prevención con Dieta Mediterránea (PREDIMED) study

    Am J Clin Nutr

    (2019)
  • N.S. Kakoly et al.

    Cardiometabolic risks in PCOS: a review of the current state of knowledge

    Expert Rev Endocrinol Metab

    (2019)
  • R.A. Wild et al.

    Assessment of cardiovascular risk and prevention of cardiovascular disease in women with the polycystic ovary syndrome: a consensus statement by the Androgen Excess and Polycystic Ovary Syndrome (AE-PCOS) Society

    J Clin Endocrinol Metab

    (2010)
  • E. Diamanti-Kandarakis et al.

    Insulin resistance and the polycystic ovary syndrome revisited: an update on mechanisms and implications

    Endocr Rev

    (2012)
  • E. Carmina et al.

    Is there really increased cardiovascular morbidity in women with polycystic ovary syndrome?

    J Womens Health (Larchmt)

    (2018)
  • A.Y. Chang et al.

    Influence of race/ethnicity on cardiovascular risk factors in polycystic ovary syndrome, the Dallas Heart Study

    Clin Endocrinol (Oxf)

    (2016)
  • D.A. Ehrmann et al.

    PCOS/Troglitazone Study Group. Effects of race and family history of type 2 diabetes on metabolic status of women with polycystic ovary syndrome

    J Clin Endocrinol Metab

    (2005)
  • U. Ezeh et al.

    Racial and ethnic differences in the metabolic response of polycystic ovary syndrome

    Clin Endocrinol (Oxf)

    (2020)
  • C.A. Gomez-Meade et al.

    Cardiometabolic health among gastric bypass surgery patients with polycystic ovarian syndrome

    World J Diabetes

    (2013)
  • M. Hara et al.

    Insulin resistance is attenuated in women with polycystic ovary syndrome with the Pro(12)Ala polymorphism in the PPARgamma gene

    J Clin Endocrinol Metab

    (2002)
  • K.W. Koval et al.

    Higher high-density lipoprotein cholesterol in African-American women with polycystic ovary syndrome compared with Caucasian counterparts

    J Clin Endocrinol Metab

    (2010)
  • A. Kumar et al.

    Prevalence of adrenal androgen excess in patients with the polycystic ovary syndrome (PCOS)

    Clin Endocrinol (Oxf)

    (2005)
  • S. Sam et al.

    Metabolic dysfunction in obese Hispanic women with polycystic ovary syndrome

    Hum Reprod

    (2015)
  • C.K. Welt et al.

    Defining constant versus variable phenotypic features of women with polycystic ovary syndrome using different ethnic groups and populations

    J Clin Endocrinol Metab

    (2006)
  • H. Mani et al.

    Clinical characteristics of polycystic ovary syndrome: investigating differences in White and South Asian women

    Clin Endocrinol (Oxf)

    (2015)
  • J.C. Lo et al.

    Epidemiology and adverse cardiovascular risk profile of diagnosed polycystic ovary syndrome

    J Clin Endocrinol Metab

    (2006)
  • N.S. Kakoly et al.

    Ethnicity, obesity and the prevalence of impaired glucose tolerance and type 2 diabetes in PCOS: a systematic review and meta-regression

    Hum Reprod Update

    (2018)
  • H.J. Teede et al.

    Recommendations from the international evidence-based guideline for the assessment and management of polycystic ovary syndrome

    Hum Reprod

    (2018)
  • Resident population and net change, V2019. Population Estimates Program: United States Department of Commerce

    (2019)
  • A.M. Matsumoto et al.

    Serum testosterone assays--accuracy matters

    J Clin Endocrinol Metab

    (2004)
  • M. Kazemi et al.

    A randomized controlled trial of a lifestyle intervention with longitudinal follow-up on ovarian dysmorphology in women with polycystic ovary syndrome

    Clin Endocrinol (Oxf)

    (2020)
  • M. Kazemi et al.

    Obesity, insulin resistance, and hyperandrogenism mediate the link between poor diet quality and ovarian dysmorphology in reproductive-aged women

    Nutrients

    (2020)
  • Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD). NICHD strategic Plan 2020....
  • R. Chatterjee et al.

    Non-traditional risk factors are important contributors to the racial disparity in diabetes risk: the atherosclerosis risk in communities study

    J Gen Intern Med

    (2014)
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