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2022, Number S5

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Cardiovasc Metab Sci 2022; 33 (S5)

Autoimmune and inflammatory diseases

Puente-Barragán, Adriana1; Espínola-Zavaleta, Nilda2; Fernández-Badillo, Valente3; Valdés-Becerril, Georgina4
Full text How to cite this article 10.35366/108061

DOI

DOI: 10.35366/108061
URL: https://dx.doi.org/10.35366/108061

Language: English
References: 10
Page: s487-489
PDF size: 159.58 Kb.


Key words:

No keywords





INTRODUCTION

The prevalence of autoimmune diseases (AI) is around 4%. It is more common in women (78-80%), with a higher incidence of cardiovascular disease (CVD), which is considered an emerging or gender-specific cardiovascular risk factor (CVRF). There is an increased immune and inflammatory response, suggesting an involvement of the sex chromosome and sex hormones. Risk factors (RF) and poor lifestyles, immune system disorders, chronic systemic inflammation, endothelial dysfunction, increased oxidative stress, and accelerated atherosclerosis (atherosclerotic cardiovascular disease - ACVD) at the coronary artery level and microvessels. The risk of developing ACVD shows a linear relationship with the activity and severity of AI, higher in women < 40 and with SLE. The risk of ACVD in rheumatoid arthritis (RA) is 1.5 to 2, psoriatic arthritis (PSA) 1.5 to 1.7, systemic lupus erythematosus (SLE) 2 to 3, and 2 to 12 in vasculitis. They can present valvular, pericardial disease, myocarditis, fibrosis, heart failure (HF), and arrhythmias. RA and SLE are more likely to develop left ventricular hypertrophy (LVH) (RR 6.5 and 4, respectively).1-3 Nonsteroidal anti-inflammatory drugs (NSAID) and corticosteroids reduce inflammation and cause dyslipidemia, hyperglycemia, obesity, and hypertension. Biological immunosuppressants as anti-TNF (adalimumab, etanercept, infliximab) and non-TNF (abatacept, anakinra, and rituximab) reduce CVR (< 30%) (suppress inflammatory state and improve endothelial function), the same as disease-modifying drugs (DMD) (hydroxychloroquine, methotrexate, and sulfasalazine).1,4

In women with intermediate CVR (according to the risk calculator for CVD of the American Heart College), the existence of AI should be considered a "risk increaser or potentiator". The available tools underestimate the existing CVR by 12 to 20%.1,4 The Interamerican Society of Cardiology (SIAC),4 in the guide on primary prevention of cardiovascular disease in women, recommends:

  • 1. Calculation of CVR and controlling CVRF (recommendation class IIb, evidence level A).
  • 2. Healthy lifestyles (recommendation class I, evidence level B).
  • 3. Apply in RA a correction factor of 1.5 on the risk calculation score and search for subclinical atherosclerosis (recommendation class IIa, evidence level B).
  • 4. Regular blood pressure measurement is recommended, and if necessary, implement treatment (recommendation class I, evidence level B).



TREATMENT, MONITORING, AND PREVENTION OF CARDIOVASCULAR DISORDERS

The drugs used in AI pose a high risk of complications and systemic and CV adverse effects1,5,6 (Table 1).



NON-INVASIVE CARDIOVASCULAR IMAGING

Noninvasive imaging methods assess disease activity, treatment effects, and complications.7

Echocardiography shows valvular involvement (30-70%), pulmonary arterial hypertension (20-30%), pericardial effusion (30%), mobility alterations, and subclinical systolic/diastolic dysfunction (30%).3,7-9 Single photon emission tomography (SPECT) and positron emission tomography (PET), nuclear magnetic resonance (NMR), and computed tomography (CT) allow an anatomical assessment of the coronary tree and great vessels (inflammation) and functional (ischemia).10



CONCLUSIONS

Autoimmune diseases confer high cardiovascular risk in women. The calculation of the CVR and intensification of the CVRF are essential. CV imaging is helpful in the diagnosis of complications and follow-up. Management requires multidisciplinary intervention to reduce cardiovascular morbidity and mortality.


REFERENCES

  1. Moran C, Collins L, Beydoun N, Mehta P, Fatade Y, Isiadinso I et al. Cardiovascular implications of immune disorders in women. Circ Res. 2022; 130: 593-610.

  2. Restivo V, Candiloro E, Daidone M, Norrito R, Cataldi M, Minutolo G et al. Systematic review and meta-analysis of cardiovascular risk in rheumatological disease: symptomatic and non-symptomatic events in rheumatoid arthritis and systemic lupus erythematosus. Autoimmun Rev. 2022; 21: 1-10.

  3. Giollo A, Cioffi G, Ognibeni F, Bixio R, Fassio A, Adami GH et al. Sex-specific association of left ventricular hypertrophy with rheumatoid arthritis. Front Cardiovasc Med. 2021; 8: 676076.

  4. Del-Sueldo M, Mendonca-Rivera MA, Sánchez-Zambrano MB, Zilberman J, Múnera-Echeverri A, Paniagua M et al. Guía de práctica clínica de la Sociedad Interamericana de Cardiología sobre prevención primaria de enfermedad cardiovascular en la mujer. Arch Cardiol Mex. 2022; 92 (Supl): 1-68.

  5. Tanaka Y. State-of-the-art treatment of systemic lupus erythematosus. Review Int J Rheum Dis. 2020; 23: 465-471.

  6. Fraenkel L, Bathon J, England B, St.Clair W, Arayssi T, Carandang K et al. 2021 American College of Rheumatology Guideline for the treatment of rheumatoid arthritis. Arthritis Care Res (Hoboken). 2021; 73: 924-939.

  7. Ikonomidis I, Makavos G, Katsimbri P, Boumpas DT, Parissis J, Iliodromitis E. Imaging risk in multisystem inflammatory diseases. JACC Cardiovasc Imaging. 2019; 12: 2517-2537.

  8. Chen J, Tang Y, Zhu M, Xu A. Heart involvement in systemic lupus erythematosus: a systemic review and meta-analysis. Clin Rheumatol. 2016; 35: 2437-2448.

  9. Silveira LH. Cardiovascular manifestations of systemic vasculitides. Curr Rheumatol Rep. 2020; 22: 72.

  10. Mavrogeni SI, Sfikakis PP, Koutsogeorgopoulou L, Markousis G, Dimitroulas T, Kolovou G et al. Cardiac tissue characterization, and imaging in autoimmune rheumatic diseases. JACC Cardiovasc Imaging. 2017; 10: 1387-1396.



AFFILIATIONS

1 Head of the Medical Section of Cardiology, CMN 20 de Noviembre, ISSSTE.

2 Echocardiography Service, "Ignacio Chávez" National Institute of Cardiology.

3 Pregraduate intern in social service in clinical research. Department of Cardiology, National Institute of Cardiology "Ignacio Chavez".

4 Cardiology Service, Central Military Hospital. ANCAM and SMC Full Member.



CORRESPONDENCE

Adriana Puente-Barragán. E-mail: adripuente@yahoo.com


Table 1

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C?MO CITAR (Vancouver)

Cardiovasc Metab Sci . 2022;33