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Abstract Number: 704

Metabolomics Analysis of Insulin Resistance in Mild/Inactive Non-Diabetic Systemic Lupus Erythematosus Women

Claudia Mendoza Pinto1, Mario García-Carrasco2, Gerardo Díaz-Merino3, Pamela Soto-Santillan4, Rossy Mejia-Ocampo5, Pamela Munguía-Realpozo3 and Alejandro Ruiz-Arguelles5, 1Systemic Autoimmune Diseases Research Unit,, UMAE, HE CMN Manuel Ávila Camacho-CIBIOR, Instituto Mexicano del Seguro Social, Puebla, Mexico, 2Systemic Autoimmune Diseases Research Unit, HGR 36-CIBIOR Instituto Mexicano del Seguro Social, Puebla, Mexico, 3Systemic Autoimmune Diseases Research Unit,, Hospital de Especialidades UMAE CMN, Instituto Mexicano del Seguro Social, Puebla, Mexico, 4Systemic Autoimmune Diseases Research Unit, Medicine School, Benemérita Universidad Autónoma de Puebla, Puebla, Mexico, 5Laboratorios Clínicos de Puebla, Puebla, Mexico

Meeting: 2018 ACR/ARHP Annual Meeting

Keywords: insulin resistance, metabolic syndrome, metabolomics and systemic lupus erythematosus (SLE)

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Session Information

Date: Sunday, October 21, 2018

Title: Systemic Lupus Erythematosus – Clinical Poster I: Clinical Manifestations and Comorbidity

Session Type: ACR Poster Session A

Session Time: 9:00AM-11:00AM

Background/Purpose: SLE patients present a higher prevalence of insulin resistance (IR) and metabolic syndrome (MetS) than age- and sex-matched healthy controls. Advances in technology are enabling evaluation for the prevention and early detection of those morbidities. Quantose IR is a simple test for IR based on a single fasting blood sample and may have value as an early indicator of risk for the development of prediabetes and type 2 diabetes mellitus (T2DM). The objective of this study was to evaluate IR in non-diabetic SLE women using metabolite markers identified using high-throughput metabolomic techniques.

Methods: SLE patients were consecutively enrolled in a cross-sectional study. A metabolomic approach using ultra-high performance liquid chromatography coupled with high-resolution mass spectrometry (UHPLC-HRMS) was developed in serum samples from non-diabetic SLE women. Activity (SLEDAI-2K) and damage (SLICC) index scores, as well as carotid intima-media thickness (IMT), were determined in SLE patients. Patients with a Quantose IR score of ≥ 63 were defined as IR. MetS was evaluated according to the NCEP-ATP III criteria.

Results: We enrolled 70 SLE patients with a mean ± SD age of 39.3±10.6 years and median disease duration of 11 years (IQR: 8-14). Fourty-five of 70 (64.2%) and 27 (38.5%) SLE patients were found to have IR and Mets, respectively. The median Quantose IR score was 69 (IQR 52.7-80.0). Patients with IR had a higher body mass index (BMI) than those without IR (27 vs. 23.7; p = 0.001). Hypertension was more frequently found in patients with IR (33.3% vs. 8.0%; p = 0.02). The SLICC index and disease activity were not associated with the Quantose IR Score. The prevalence of a Quantose IR score ≥ 63 was higher in patients with MetS (81.5% vs. 53.5%; p = 0.02). Quantose IR score also correlated with the number of metabolic syndrome criteria (r= 0.35, p= 0.003). Carotid IMT values were not correlated with the IR index.

Conclusion: In non-diabetic SLE women, the prevalence of IR based on Quantose IR was 64.2% using UHPLC-HRMS. Although, some traditional IR factors, such as BMI and hypertension were associated with IR in these patients, SLE-related factors were not. Moreover, Quantose IR score may related to MetS in those patients.


Disclosure: C. Mendoza Pinto, None; M. García-Carrasco, None; G. Díaz-Merino, None; P. Soto-Santillan, None; R. Mejia-Ocampo, None; P. Munguía-Realpozo, None; A. Ruiz-Arguelles, None.

To cite this abstract in AMA style:

Mendoza Pinto C, García-Carrasco M, Díaz-Merino G, Soto-Santillan P, Mejia-Ocampo R, Munguía-Realpozo P, Ruiz-Arguelles A. Metabolomics Analysis of Insulin Resistance in Mild/Inactive Non-Diabetic Systemic Lupus Erythematosus Women [abstract]. Arthritis Rheumatol. 2018; 70 (suppl 9). https://acrabstracts.org/abstract/metabolomics-analysis-of-insulin-resistance-in-mild-inactive-non-diabetic-systemic-lupus-erythematosus-women/. Accessed .
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