The relation between ischemia modified albumin levels and carotid intima media thickness in patients with rheumatoid arthritis.


Journal

International journal of rheumatic diseases
ISSN: 1756-185X
Titre abrégé: Int J Rheum Dis
Pays: England
ID NLM: 101474930

Informations de publication

Date de publication:
Jan 2019
Historique:
pubmed: 31 3 2016
medline: 30 5 2019
entrez: 31 3 2016
Statut: ppublish

Résumé

Cardiovascular diseases, among which atherosclerotic heart disease, are known to be one of the most important mortality and morbidity causes in patients with rheumatoid arthritis (RA). Ischemia modified albumin (IMA) is a potential marker that can be used to assess atherosclerosis-related myocardial ischemia. Another frequently used marker for the assessment of atherosclerotic lesions is the carotid intima media thickness (CIMT). To evaluate the role that IMA has on atherosclerosis development and its clinical usability in patients with RA, by assessing the values of IMA and CIMT. Our prospective study was conducted between June 2012 and March 2013 at the Rheumatology Department of Necmettin Erbakan Meram Medical School, Turkey. Fifty-two RA patients, diagnosed according to the 1987 criteria of the American College of Rheumatology, and an age- and sex-matched control group of 46 healthy subjects were included in this study. No significant difference was detected between the groups with respect to age, sex and body mass index. In the patient group the IMA and CIMT values were found to be 0.37 ± 0.12 absorbance units (ABSU) and 0.80 ± 0.22 mm, respectively, while in the control group they were 0.31 ± 0.11 ABSU and 0.51 ± 0.18 mm, respectively. The IMA and CIMT values were significantly higher in the patient group (P = 0.022 and P < 0.0001, respectively). A positive correlation was found between IMA, CIMT and Disease Activity Score of 28 joints (P = 0.016 and P = 0.002, respectively). Since the values of IMA were higher in the patient group compared to controls and because of its correlation with CIMT, we suggest the use of IMA as an early marker of atherosclerosis in RA patients.

Sections du résumé

BACKGROUND BACKGROUND
Cardiovascular diseases, among which atherosclerotic heart disease, are known to be one of the most important mortality and morbidity causes in patients with rheumatoid arthritis (RA). Ischemia modified albumin (IMA) is a potential marker that can be used to assess atherosclerosis-related myocardial ischemia. Another frequently used marker for the assessment of atherosclerotic lesions is the carotid intima media thickness (CIMT).
AIM OBJECTIVE
To evaluate the role that IMA has on atherosclerosis development and its clinical usability in patients with RA, by assessing the values of IMA and CIMT.
METHODS AND MATERIALS METHODS
Our prospective study was conducted between June 2012 and March 2013 at the Rheumatology Department of Necmettin Erbakan Meram Medical School, Turkey. Fifty-two RA patients, diagnosed according to the 1987 criteria of the American College of Rheumatology, and an age- and sex-matched control group of 46 healthy subjects were included in this study.
RESULTS RESULTS
No significant difference was detected between the groups with respect to age, sex and body mass index. In the patient group the IMA and CIMT values were found to be 0.37 ± 0.12 absorbance units (ABSU) and 0.80 ± 0.22 mm, respectively, while in the control group they were 0.31 ± 0.11 ABSU and 0.51 ± 0.18 mm, respectively. The IMA and CIMT values were significantly higher in the patient group (P = 0.022 and P < 0.0001, respectively). A positive correlation was found between IMA, CIMT and Disease Activity Score of 28 joints (P = 0.016 and P = 0.002, respectively).
CONCLUSION CONCLUSIONS
Since the values of IMA were higher in the patient group compared to controls and because of its correlation with CIMT, we suggest the use of IMA as an early marker of atherosclerosis in RA patients.

Identifiants

pubmed: 27028097
doi: 10.1111/1756-185X.12851
doi:

Substances chimiques

Biomarkers 0
ischemia-modified albumin 0
Serum Albumin, Human ZIF514RVZR

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

32-37

Commentaires et corrections

Type : CommentIn

Informations de copyright

© 2016 Asia Pacific League of Associations for Rheumatology and John Wiley & Sons Australia, Ltd.

Auteurs

Ali U Uslu (AU)

Department of Internal Medicine, Eskisehir Military Hospital, Eskisehir, Turkey.

Adem Kucuk (A)

Division of Rheumatology, Necmettin Erbakan University, Konya, Turkey.

Sevket Balta (S)

Department of Cardiology, Gulhane Medical Faculty, Ankara, Turkey.

Cengiz Ozturk (C)

Department of Cardiology, Gulhane Medical Faculty, Ankara, Turkey.

Sevket Arslan (S)

Division of Allergy and Clinical Immunology, Necmettin Erbakan University, Konya, Turkey.

Levent Tekin (L)

Department of Physical Medicine and Rehabilitation, Beyhekim State Hospital, Konya, Turkey.

Sami Kucuksen (S)

Department of Physical Medicine and Rehabilitation, Necmettin Erbakan University, Konya, Turkey.

Aysun Toker (A)

Department of Biochemistry, Necmettin Erbakan University, Konya, Turkey.

Mehmet Kayrak (M)

Department of Cardiology, Necmettin Erbakan University, Konya, Turkey.

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Classifications MeSH