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Dyslipidemia is insufficiently treated in antiphospholipid syndrome patients.
Yelnik, Cécile M; Martin, Claire; Ledoult, Emmanuel; Sanges, Sébastien; Sobanski, Vincent; Farhat, Meryem; Morell-Dubois, Sandrine; Maillard, Hélène; Drumez, Elodie; Launay, David; Hachulla, Eric; Lambert, Marc.
Affiliation
  • Yelnik CM; 27023University of Lille, CHU Lille, Département de Médecine Interne et d'Immunologie Clinique, Centre National de Référence Maladies Systémiques et Auto-immunes Rares Nord et Nord-Ouest de France (CeRAINO), European Reference Network on Rare Connective Tissue and Musculoskeletal Diseases Network (R
  • Martin C; INSERM, UMR 1167, RID-AGE, Lille, France.
  • Ledoult E; 27023University of Lille, CHU Lille, ULR 2694 - METRICS: Évaluation des technologies de santé et des pratiques médicales, Lille, France.
  • Sanges S; 27023University of Lille, CHU Lille, Département de Médecine Interne et d'Immunologie Clinique, Centre National de Référence Maladies Systémiques et Auto-immunes Rares Nord et Nord-Ouest de France (CeRAINO), European Reference Network on Rare Connective Tissue and Musculoskeletal Diseases Network (R
  • Sobanski V; INSERM, U1286, INFINITE - Institute for Translational Research in Inflammation, Lille, France.
  • Farhat M; 27023University of Lille, CHU Lille, Département de Médecine Interne et d'Immunologie Clinique, Centre National de Référence Maladies Systémiques et Auto-immunes Rares Nord et Nord-Ouest de France (CeRAINO), European Reference Network on Rare Connective Tissue and Musculoskeletal Diseases Network (R
  • Morell-Dubois S; INSERM, U1286, INFINITE - Institute for Translational Research in Inflammation, Lille, France.
  • Maillard H; 27023University of Lille, CHU Lille, Département de Médecine Interne et d'Immunologie Clinique, Centre National de Référence Maladies Systémiques et Auto-immunes Rares Nord et Nord-Ouest de France (CeRAINO), European Reference Network on Rare Connective Tissue and Musculoskeletal Diseases Network (R
  • Drumez E; INSERM, U1286, INFINITE - Institute for Translational Research in Inflammation, Lille, France.
  • Launay D; 27023University of Lille, CHU Lille, Département de Médecine Interne et d'Immunologie Clinique, Centre National de Référence Maladies Systémiques et Auto-immunes Rares Nord et Nord-Ouest de France (CeRAINO), European Reference Network on Rare Connective Tissue and Musculoskeletal Diseases Network (R
  • Hachulla E; INSERM, U1286, INFINITE - Institute for Translational Research in Inflammation, Lille, France.
  • Lambert M; 27023University of Lille, CHU Lille, Département de Médecine Interne et d'Immunologie Clinique, Centre National de Référence Maladies Systémiques et Auto-immunes Rares Nord et Nord-Ouest de France (CeRAINO), European Reference Network on Rare Connective Tissue and Musculoskeletal Diseases Network (R
Lupus ; 31(11): 1379-1384, 2022 Oct.
Article in En | MEDLINE | ID: mdl-35822929
ABSTRACT

OBJECTIVES:

Although dyslipidemia is a strong risk factor for thrombosis in antiphospholipid syndrome (APS), it has been poorly studied. This study aimed to assess lipids profile and risk factors for unachieved cholesterol levels in a real-life APS population.

METHODS:

Inclusion criteria were APS diagnosis according to international classification criteria, referring to the out-patients clinic of our tertiary care center for their follow-up, and having a blood sample collection for lipids levels determination. Cholesterol level targets for each patient were defined according to 2019 ESC/EAS guidelines for the management of dyslipidemia.

RESULTS:

Between January 2020 and April 2021, 114 APS patients were included (male 37 (32.5%); mean age 49 ± 14 years). Among them, 40 (35.1%) had a history of dyslipidemia, 48 (42.1%) were under lipid-lowering therapies, and 59 (51.8%) had a history of cardiovascular disease (CVD). Mean levels of low-density lipoprotein cholesterol (LDL-C), high-density lipoprotein cholesterol (HDL-C), and triglyceride were, respectively, 110 ± 40 mg/dL, 60±20 mg/dL, and 120 (80-190) mg/dL. Unachieved LDL-C levels were found in 77 (67.5%) patients of whom 53 had history of CVD. Overall, 90 (78.9%) had protective HDL-C and 31 (27.2%) had hypertriglyceridemia. In the multivariate analysis, independent risk factors for unachieved LDL-C levels were older age and history of CVD; triple aPL negativity, defined as complete disappearance of aPL over time in APS patients who were previously positive in accordance to international criteria, was an independent protective factor for unachieved LDL-C.

CONCLUSION:

Our finding suggested that dyslipidemia is frequent in APS patients and mainly insufficiently treated, especially in patients with history of CVD, who are at highest risk of future CV events.
Subject(s)
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cardiovascular Diseases / Antiphospholipid Syndrome / Dyslipidemias / Lupus Erythematosus, Systemic Type of study: Etiology_studies / Guideline / Risk_factors_studies Limits: Adult / Humans / Male / Middle aged Language: En Journal: Lupus Journal subject: REUMATOLOGIA Year: 2022 Type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cardiovascular Diseases / Antiphospholipid Syndrome / Dyslipidemias / Lupus Erythematosus, Systemic Type of study: Etiology_studies / Guideline / Risk_factors_studies Limits: Adult / Humans / Male / Middle aged Language: En Journal: Lupus Journal subject: REUMATOLOGIA Year: 2022 Type: Article