impact factor, citescore
logo
 

Diagnosis

 

Abdominal adipose tissue predicts major cardiovascular events in systemic necrotising vasculitides


1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13

 

  1. Department of Rheumatology, Hôpital Cochin, Paris; INSERM UMR-1153, Paris; Université Paris Descartes, Faculté de Médecine Paris Descartes, France.
  2. Université Paris Descartes, Faculté de Médecine Paris Descartes; Department of Internal Medicine, Hôpital Cochin, Paris; National Referral Centre for Systemic and Autoimmune Diseases, Hôpital Cochin, Paris, France.
  3. Department of Internal Medicine, Hôpital Cochin, Paris; National Referral Centre for Systemic and Autoimmune Diseases, Hôpital Cochin, Paris, France.
  4. Department of Rheumatology, Hôpital Cochin, Paris, France.
  5. Department of Rheumatology, Hôpital Cochin, Paris, France.
  6. Université Paris Descartes, Faculté de Médecine Paris Descartes; Department of Internal Medicine, Hôpital Cochin, Paris; National Referral Centre for Systemic and Autoimmune Diseases, Hôpital Cochin, Paris, France.
  7. Université Paris Descartes, Faculté de Médecine Paris Descartes; Department of Internal Medicine, Hôpital Cochin, Paris; National Referral Centre for Systemic and Autoimmune Diseases, Hôpital Cochin, Paris, France.
  8. Université Paris Descartes, Faculté de Médecine Paris Descartes; Department of Internal Medicine, Hôpital Cochin, Paris; National Referral Centre for Systemic and Autoimmune Diseases, Hôpital Cochin, Paris, France.
  9. Université Paris Descartes, Faculté de Médecine Paris Descartes; Department of Internal Medicine, Hôpital Cochin, Paris; National Referral Centre for Systemic and Autoimmune Diseases, Hôpital Cochin, Paris, France.
  10. Université Paris Descartes, Faculté de Médecine Paris Descartes; Department of Internal Medicine, Hôpital Cochin, Paris; National Referral Centre for Systemic and Autoimmune Diseases, Hôpital Cochin, Paris, France.
  11. Department of Rheumatology, Hôpital Cochin, Paris; INSERM UMR-1153, Paris, France.
  12. Université Paris Descartes, Faculté de Médecine Paris Descartes; Department of Internal Medicine, Hôpital Cochin, Paris; National Referral Centre for Systemic and Autoimmune Diseases, Hôpital Cochin, Paris, France.
  13. Université Paris Descartes, Faculté de Médecine Paris Descartes; Department of Internal Medicine, Hôpital Cochin, Paris; National Referral Centre for Systemic and Autoimmune Diseases, Hôpital Cochin, Paris, France. benjamin.terrier@aphp.fr

for the French Vasculitis Study Group (FVSG)

CER12241
2019 Vol.37, N°2 ,Suppl.117
PI 0130, PF 0136
Diagnosis

Free to view
(click on article PDF icon to read the article)

PMID: 31162033 [PubMed]

Received: 17/03/2019
Accepted : 08/05/2019
In Press: 21/05/2019
Published: 21/05/2019

Abstract

OBJECTIVES:
Cardiovascular (CV) events are highly prevalent in systemic necrotising vasculitides (SNV). Visceral/subcutaneous adipose tissue (VAT/SAT) ratio has been shown to be associated with CV events in various diseases. We aimed to assess the relevance of abdominal adipose tissue measurement to predict major CV events (MCVEs) in SNV.
METHODS:
Patients with SNV were successively included in a longitudinal study assessing MCVEs and other sequelae. Dual x-ray absorptiometry was performed to evaluate abdominal adipose tissue. Patients were prospectively followed for MCVEs, defined as myocardial infarction, unstable angina, stroke, arterial revascularisation and/or hospitalisation for or death from CV causes.
RESULTS:
One hundred and twenty consecutive SNV patients were included and analysed (54 males, mean age 53±18 years). High CV risk was found in 28 (23.3%) patients. In univariate analysis, age, male gender, VDI, VAT/SAT ratio and serum troponin level were significantly associated with high CV risk, whereas age and VAT/SAT ratio remained independently associated with high CV risk. Variables associated with high tertile of VAT/SAT ratio included age and metabolic risk factors. After median follow-up of 42 months, 19 (16%) patients experienced MCVEs. Hazard ratios for incident MCVEs compared with 1st tertile of VAT/SAT ratio were 7.22 (1.02–51.3; p=0.048) and 9.90 (3.15–31.2; p=0.0002) in the 2nd and 3rd tertile, respectively.
CONCLUSIONS:
Abdominal visceral adipose tissue is a reliable surrogate marker of CV risk and predicts incident MCVEs in SNV patients. Abdominal adipose tissue should be probably evaluated routinely in these patients to assess CV risk.

Rheumatology Article

Rheumatology Addendum