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      Associations Between the Cyclic Guanosine Monophosphate Pathway and Cardiovascular Risk Factors: MESA

      research-article
      , MD 1 , , , PhD 2 , , MBBS 1 , , MBBS, MPH 3 , , MBBS, PhD 2 , 4 , , MD, PhD 1 , 2 , , MD, DrPH 2 , , MD 1 , , MD 5 , , MD 1 , , PhD 6 , , MD, MBA 1 , , MD, PhD 7 , , MD 8 , , MD, MS 1 , 2 , , MD, MHS 1 , 2
      Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease
      John Wiley and Sons Inc.
      cardiovascular disease risk factors, cGMP, epidemiology, N‐terminal pro‐B type NP, sex hormones, Biomarkers, Heart Failure, Epidemiology, Risk Factors

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          Abstract

          Background

          cGMP mediates numerous cardioprotective functions and is a potential therapeutic target for cardiovascular disease. Preclinical studies suggest that plasma cGMP is reflective of natriuretic peptide stimulation. Epidemiologic associations between c GMP and natriuretic peptide, as well as cardiovascular disease risk factors, are unknown.

          Methods and Results

          We measured plasma cGMP in 542 men and 496 women free of cardiovascular disease and heart failure in MESA (Multi‐Ethnic Study of Atherosclerosis). Cross‐sectional associations of N‐terminal pro‐B type natriuretic peptide, sex hormones, and cardiovascular disease/heart failure risk factors with log( cGMP) were analyzed using multivariable linear regression models. Mean ( SD) cGMP was 4.7 (2.6) pmol/mL, with no difference between the sexes. After adjusting for cardiovascular risk factors, N‐terminal pro‐B type natriuretic peptide was significantly positively associated with cGMP ( P<0.05). Higher blood pressure and lower estimated glomerular filtration rate were associated with higher cGMP ( P<0.05). Triglyceride levels, total/high‐density lipoprotein cholesterol ratio, presence of diabetes mellitus, and the homeostatic model assessment of insulin resistance were inversely associated with cGMP ( P<0.05). Among women, free testosterone and dehydroepiandrosterone were inversely associated with cGMP, while sex hormone binding globulin was positively associated ( P<0.05).

          Conclusions

          In a community‐cohort, plasma cGMP was associated with natriuretic peptide signaling. Higher blood pressure and greater renal dysfunction were positively associated with cGMP, while adverse metabolic risk factors were inversely associated. Increased androgenicity in postmenopausal women was inversely associated with cGMP. These novel associations further our understanding of the role of cGMP in a general population.

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          Most cited references33

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          Natriuretic peptides.

          Natriuretic peptides (NPs) are released from the heart in response to pressure and volume overload. B-type natriuretic peptide (BNP) and N-terminal-proBNP have become important diagnostic tools for assessing patients who present acutely with dyspnea. The NP level reflects a compilation of systolic and diastolic function as well as right ventricular and valvular function. Studies suggest that using NPs in the emergency department can reduce the consumption of hospital resources and can lower costs by either eliminating the need for other, more expensive tests or by establishing an alternative diagnosis that does not require hospital stay. Caveats such as body mass index and renal function must be taken into account when analyzing NP levels. Natriuretic peptide levels have important prognostic value in multiple clinical settings, including in patients with stable coronary artery disease and with acute coronary syndromes. In patients with decompensated heart failure due to volume overload, a treatment-induced drop in wedge pressure is often accompanied by a rapid drop in NP levels. Knowing a patient's NP levels might thus assist with hemodynamic assessment and subsequent treatment titration. Monitoring NP levels in the outpatient setting might also improve patient care and outcomes.
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            Endogenous Sex Hormones and Incident Cardiovascular Disease in Post-Menopausal Women

            Background Higher androgen and lower estrogen levels are associated with cardiovascular disease (CVD) risk factors in women. However, studies on sex hormones and incident CVD events in women have yielded conflicting results. Objectives We assessed the associations of sex hormone levels with incident CVD, coronary heart disease (CHD), and heart failure (HF) events among women without CVD at baseline. Methods We studied 2,834 post-menopausal women participating in MESA with testosterone, estradiol, dehydroepiandrosterone, and sex hormone binding globulin (SHBG) levels measured at baseline (2000–2002). We used Cox hazard models to evaluate associations of sex hormones with each outcome, adjusting for demographics, CVD risk factors, and hormone therapy use. Results The mean (SD) age was 64.9 (8.9) years. During 12.1 years of follow-up, 283 CVD, 171 CHD, and 103 HF incident events occurred. In multivariable-adjusted models, the Hazard Ratios (95% CI) associated with 1 SD greater log-transformed sex hormone level for the respective outcomes of CVD, CHD, and HF were as follows: Total testosterone: 1.14 (1.01–1.29), 1.20 (1.03–1.40), 1.09 (0.90–1.34); Estradiol: 0.94 (0.80–1.11), 0.77 (0.63–0.95), 0.78 (0.60–1.02); Testosterone/Estradiol ratio: 1.19 (1.02–1.40), 1.45 (1.19–1.78), 1.31 (1.01–1.70). Dehydroepiandrosterone and SHBG levels were not associated with these outcomes. Conclusions Among post-menopausal women, a higher testosterone/estradiol ratio was associated with an elevated risk for incident CVD, CHD, and HF events, higher levels of testosterone associated with increased CVD and CHD, while higher estradiol levels were associated with a lower CHD risk. Sex hormones levels after menopause are associated with women’s increased CVD risk later in life. Condensed abstract We studied 2,834 post-menopausal women in the Multi-Ethnic Study of Atherosclerosis. Higher total testosterone/estradiol ratio was independently associated with an elevated risk for incident CVD, CHD, and HF events. After >12 years of follow-up, the multivariable-adjusted Hazard Ratios (95% CI) associated with 1 SD greater log-transformed total testosterone/estradiol ratio for incident CVD, CHD and HF events were 1.19 (1.02–1.40), 1.45 (1.19–1.78), 1.31 (1.01–1.70), respectively. Sex hormones levels after menopause are associated with women’s increased CVD risk later in life.
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              Cyclic GMP signaling in cardiovascular pathophysiology and therapeutics.

              Cyclic guanosine 3',5'-monophosphate (cGMP) mediates a wide spectrum of physiologic processes in multiple cell types within the cardiovascular system. Dysfunctional signaling at any step of the cascade - cGMP synthesis, effector activation, or catabolism - have been implicated in numerous cardiovascular diseases, ranging from hypertension to atherosclerosis to cardiac hypertrophy and heart failure. In this review, we outline each step of the cGMP signaling cascade and discuss its regulation and physiologic effects within the cardiovascular system. In addition, we illustrate how cGMP signaling becomes dysregulated in specific cardiovascular disease states. The ubiquitous role cGMP plays in cardiac physiology and pathophysiology presents great opportunities for pharmacologic modulation of the cGMP signal in the treatment of cardiovascular diseases. We detail the various therapeutic interventional strategies that have been developed or are in development, summarizing relevant preclinical and clinical studies.
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                Author and article information

                Contributors
                wying1@jhmi.edu
                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
                16 December 2019
                17 December 2019
                : 8
                : 24 ( doiID: 10.1002/jah3.v8.24 )
                : e013149
                Affiliations
                [ 1 ] Division of Cardiology Department of Medicine Johns Hopkins University School of Medicine Baltimore MD
                [ 2 ] Department of Epidemiology Johns Hopkins University Bloomberg School of Public Health Baltimore MD
                [ 3 ] Department of Epidemiology Emory University Rollins School of Public Health Atlanta GA
                [ 4 ] Division of General Internal Medicine Department of Medicine Johns Hopkins University School of Medicine Baltimore MD
                [ 5 ] Division of Cardiology Department of Medicine Northwestern University Feinberg School of Medicine Chicago IL
                [ 6 ] Division of Atherosclerosis & Vascular Medicine Department of Medicine Baylor College of Medicine Houston TX
                [ 7 ] Cardiovascular Health Research Unit and Department of Epidemiology University of Washington Seattle WA
                [ 8 ] Inova Heart and Vascular Institute Falls Church VA
                Author notes
                [*] [* ] Correspondence to: Wendy Ying, MD, 600 North Wolfe Street, Halsted 500, Baltimore, MD 21287. E‐mail: wying1@ 123456jhmi.edu
                Article
                JAH34668
                10.1161/JAHA.119.013149
                6951064
                31838972
                ad802ac3-56f0-48fb-a7f0-b88596292f32
                © 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
                : 06 May 2019
                : 23 October 2019
                Page count
                Figures: 4, Tables: 5, Pages: 17, Words: 8198
                Funding
                Funded by: American Heart Association Go Red for Women Strategically Focused Research Network
                Award ID: 16SFRN27870000
                Funded by: National Center for Advancing Translational Sciences
                Award ID: UL1‐TR‐000040
                Award ID: UL1‐TR‐001079
                Award ID: UL1‐TR‐001420
                Funded by: Johns Hopkins University
                Categories
                Original Research
                Original Research
                Epidemiology
                Custom metadata
                2.0
                jah34668
                17 December 2019
                Converter:WILEY_ML3GV2_TO_NLMPMC version:5.7.2 mode:remove_FC converted:16.12.2019

                Cardiovascular Medicine
                cardiovascular disease risk factors,cgmp,epidemiology,n‐terminal pro‐b type np,sex hormones,biomarkers,heart failure,risk factors

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