Higher body mass index and disease duration are associated with increased risk of left ventricular diastolic dysfunction in women with systemic lupus erythematosus.


Journal

Lupus
ISSN: 1477-0962
Titre abrégé: Lupus
Pays: England
ID NLM: 9204265

Informations de publication

Date de publication:
Nov 2022
Historique:
pubmed: 21 9 2022
medline: 23 11 2022
entrez: 20 9 2022
Statut: ppublish

Résumé

Patients with systemic lupus erythematosus (SLE) have an increased cardiovascular (CV) risk. Insulin resistance (IR), which is higher in patients with SLE, adversely impacts left ventricular (LV) remodeling and function. The aims were to determine LV dysfunction and evaluate the influence of potential risk factors on subclinical LV dysfunction in women with SLE, including IR. This cross-sectional study included adult women with SLE without diabetes mellitus (DM), hypertension or severe obesity. Diastolic dysfunction (DD) was verified according to current guidelines. Insulin resistance was estimated using the Quantose score. We included 77 women. The frequency of IR was 65%. All participants had a normal ejection fraction (EF), and 11 (15.7%) had abnormal LV global longitudinal strain (GLS). Twenty-three (32.8%) had DD. The GLS% and global circumferential strain (GCS)% did not differ in patients with and without IR (-20.8 ± 3.1 vs -20.5 ± 2.1; Patients with overweight/obesity may be at higher risk of LV dysfunction. Although IR was high in our patients with SLE was not associated with systolic dysfunction or DD. Body mass index and disease duration were associated with an increased risk of DD.

Sections du résumé

BACKGROUND BACKGROUND
Patients with systemic lupus erythematosus (SLE) have an increased cardiovascular (CV) risk. Insulin resistance (IR), which is higher in patients with SLE, adversely impacts left ventricular (LV) remodeling and function. The aims were to determine LV dysfunction and evaluate the influence of potential risk factors on subclinical LV dysfunction in women with SLE, including IR.
METHODS METHODS
This cross-sectional study included adult women with SLE without diabetes mellitus (DM), hypertension or severe obesity. Diastolic dysfunction (DD) was verified according to current guidelines. Insulin resistance was estimated using the Quantose score.
RESULTS RESULTS
We included 77 women. The frequency of IR was 65%. All participants had a normal ejection fraction (EF), and 11 (15.7%) had abnormal LV global longitudinal strain (GLS). Twenty-three (32.8%) had DD. The GLS% and global circumferential strain (GCS)% did not differ in patients with and without IR (-20.8 ± 3.1 vs -20.5 ± 2.1;
CONCLUSIONS CONCLUSIONS
Patients with overweight/obesity may be at higher risk of LV dysfunction. Although IR was high in our patients with SLE was not associated with systolic dysfunction or DD. Body mass index and disease duration were associated with an increased risk of DD.

Identifiants

pubmed: 36123774
doi: 10.1177/09612033221128433
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1639-1648

Auteurs

Pamela Munguía-Realpozo (P)

Rheumatology Department, Medicine School, 37767Meritorious Autonomous University of Puebla, Puebla, Mexico.
Systemic Autoimmune Diseases Research Unit-CIBIOR, Specialities Hospital, CMN, Mexican Social Security Institute, Puebla, Mexico.

Claudia Mendoza-Pinto (C)

Rheumatology Department, Medicine School, 37767Meritorious Autonomous University of Puebla, Puebla, Mexico.
Systemic Autoimmune Diseases Research Unit-CIBIOR, Specialities Hospital, CMN, Mexican Social Security Institute, Puebla, Mexico.

Mario García-Carrasco (M)

Rheumatology Department, Medicine School, 37767Meritorious Autonomous University of Puebla, Puebla, Mexico.
Systemic Autoimmune Diseases Research Unit-CIBIOR, Specialities Hospital, CMN, Mexican Social Security Institute, Puebla, Mexico.

Ricardo O Escarcega (RO)

Florida Heart Associates Heart and Vascular Institute, Fort Myers, FL, USA.

Roberto Berra-Romani (R)

Department of Biomedicine, Medicine School, 3972Meritorious Autonomous University of Puebla, Puebla, Mexico.

Ivet Etchegaray-Morales (I)

Rheumatology Department, Medicine School, 37767Meritorious Autonomous University of Puebla, Puebla, Mexico.

Liliana Pérez-Aquino (L)

Systemic Autoimmune Diseases Research Unit-CIBIOR, Specialities Hospital, CMN, Mexican Social Security Institute, Puebla, Mexico.

Adalberto Ramírez-Hernández (A)

Cardiology Service, Specialities Hospital, CMN, Mexican Social Security Institute, Puebla, Mexico.

Socorro Méndez-Martínez (S)

Research in Health Coordination, Mexican Social Security Institute, Puebla, Mexico.

Ricard Cervera (R)

Department of Autoimmune Disease, Hospital Clinic, Barcelona, Spain.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH