Disease Activity Score in 28 Joints Using GGT Permits a Dual Evaluation of Joint Activity and Cardiovascular Risk.


Journal

The Journal of rheumatology
ISSN: 0315-162X
Titre abrégé: J Rheumatol
Pays: Canada
ID NLM: 7501984

Informations de publication

Date de publication:
01 12 2020
Historique:
accepted: 25 05 2020
pubmed: 17 6 2020
medline: 24 8 2021
entrez: 17 6 2020
Statut: ppublish

Résumé

To identify the factors potentially associated with serum gamma-glutamyltransferase (GGT) elevation in patients with rheumatoid arthritis (RA). This is a cross-sectional monocentric study including RA patients over a 12-month period. Data on liver function, RA disease activity, and hepatotoxic and cardiovascular (CV) risk factors were systematically collected. To provide a simple tool to evaluate both joint disease activity and CV risk factors, we constructed the Disease Activity Score in 28 joints (DAS28)-GGT composite index by replacing erythrocyte sedimentation rate (ESR) with GGT. Among the 129 included patients, 32 (25%) had isolated GGT increase. GGT correlated with age, C-reactive protein (CRP) levels, and body weight and were significantly increased in patients with alcohol intake, type 2 diabetes mellitus, hypertension, dyslipidemia, and metabolic syndrome. GGT levels also gradually increased with the number of CV risk factors and correlated with the Framingham CV risk score. The composite index DAS28-GGT remained a reliable marker of RA disease activity and accurately detected patients with CV risk factors. Conversely to the DAS28 and the DAS28-CRP, the DAS28-GGT steadily increased according to the number of CV risk factors and had an increased diagnostic value compared to the DAS28 and DAS28-CRP for the presence of at least 2 CV risk factors and a Framingham CV risk score greater than 10%. GGT may be considered as a marker of systemic inflammation and CV risk in patients with RA. Based on these findings, we herein propose an original index, the DAS28-GGT, which is able to evaluate both joint disease activity and CV risk. This index will deserve further validation in prospective cohorts.

Identifiants

pubmed: 32541072
pii: jrheum.200185
doi: 10.3899/jrheum.200185
doi:

Substances chimiques

C-Reactive Protein 9007-41-4
gamma-Glutamyltransferase EC 2.3.2.2

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1738-1745

Commentaires et corrections

Type : CommentIn

Auteurs

Hélène Vergneault (H)

H. Vergneault, MD, E. Vandebeuque, MD, V. Codullo, MD, Y. Allanore, MD, PhD, J. Avouac, MD, PhD, Université de Paris, Service de Rhumatologie, Hôpital Cochin, AP-HP.CUP, Paris, France.

Eloïse Vandebeuque (E)

H. Vergneault, MD, E. Vandebeuque, MD, V. Codullo, MD, Y. Allanore, MD, PhD, J. Avouac, MD, PhD, Université de Paris, Service de Rhumatologie, Hôpital Cochin, AP-HP.CUP, Paris, France.

Veronica Codullo (V)

H. Vergneault, MD, E. Vandebeuque, MD, V. Codullo, MD, Y. Allanore, MD, PhD, J. Avouac, MD, PhD, Université de Paris, Service de Rhumatologie, Hôpital Cochin, AP-HP.CUP, Paris, France.

Yannick Allanore (Y)

H. Vergneault, MD, E. Vandebeuque, MD, V. Codullo, MD, Y. Allanore, MD, PhD, J. Avouac, MD, PhD, Université de Paris, Service de Rhumatologie, Hôpital Cochin, AP-HP.CUP, Paris, France.

Jérôme Avouac (J)

H. Vergneault, MD, E. Vandebeuque, MD, V. Codullo, MD, Y. Allanore, MD, PhD, J. Avouac, MD, PhD, Université de Paris, Service de Rhumatologie, Hôpital Cochin, AP-HP.CUP, Paris, France. jerome.avouac@cch.aphp.fr.

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Classifications MeSH