Dyslipidemia in Women with Autoimmune Diseases: Systemic Lupus Erythematosus, Rheumatoid Arthritis, and Beyond

Women with autoimmune diseases such as systemic lupus erythematosus (SLE), rheumatoid arthritis (RA), and others face a disproportionate burden of cardiovascular disease (CVD), in part due to inflammation-driven dyslipidemia. Unlike classical metabolic dyslipidemia, these lipid abnormalities are characterized by low high-density lipoprotein (HDL) cholesterol, elevated triglycerides, dysfunctional HDL, and increased oxidized low-density lipoprotein. The interplay of chronic inflammation, immune dysregulation, hormonal factors, and treatment-related effects contributes to a unique lipid phenotype that amplifies CVD risk in women. This narrative review explores the epidemiology, pathophysiology, and clinical manifestations of dyslipidemia in SLE and RA, with an extension to other autoimmune diseases such as psoriatic arthritis, Sjögren’s syndrome, systemic sclerosis, and autoimmune thyroid disorders. Management strategies, including early screening, inflammation control, statin therapy, and gender-specific considerations, are highlighted. The article underscores the urgent need for tailored risk assessment tools and therapeutic approaches to mitigate premature cardiovascular morbidity and mortality in this vulnerable population.

Institutions

Publication Details

Journal
Indian Journal of Cardiovascular Disease in Women
Published
2025-12-09
DOI
https://doi.org/10.25259/ijcdw_60_2025
Primary Topic
Systemic Lupus Erythematosus Research
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Dyslipidemia in Women with Autoimmune Diseases: Systemic Lupus Erythematosus, Rheumatoid Arthritis, and Beyond

Indian Journal of Cardiovascular Disease in Women
Systemic Lupus Erythematosus Research
article

Dyslipidemia in Women with Autoimmune Diseases: Systemic Lupus Erythematosus, Rheumatoid Arthritis, and Beyond

article en

Abstract

Women with autoimmune diseases such as systemic lupus erythematosus (SLE), rheumatoid arthritis (RA), and others face a disproportionate burden of cardiovascular disease (CVD), in part due to inflammation-driven dyslipidemia. Unlike classical metabolic dyslipidemia, these lipid abnormalities are characterized by low high-density lipoprotein (HDL) cholesterol, elevated triglycerides, dysfunctional HDL, and increased oxidized low-density lipoprotein. The interplay of chronic inflammation, immune dysregulation, hormonal factors, and treatment-related effects contributes to a unique lipid phenotype that amplifies CVD risk in women. This narrative review explores the epidemiology, pathophysiology, and clinical manifestations of dyslipidemia in SLE and RA, with an extension to other autoimmune diseases such as psoriatic arthritis, Sjögren’s syndrome, systemic sclerosis, and autoimmune thyroid disorders. Management strategies, including early screening, inflammation control, statin therapy, and gender-specific considerations, are highlighted. The article underscores the urgent need for tailored risk assessment tools and therapeutic approaches to mitigate premature cardiovascular morbidity and mortality in this vulnerable population.

Indian Journal of Cardiovascular Disease in WomenVol. 10
Indira Gandhi Institute of Medical Sciences (IN), Maharaja Krishna Chandra Gajapati Medical College and Hospital (IN), Advanced Pharma (US), Sri Sathya Sai Institute of Higher Medical Sciences (IN)
Good health and well-being
Openalex Percentile: Top 30%
Systemic Lupus Erythematosus Research
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.