AI Article Synopsis

  • The study aimed to explore the link between abdominal subcutaneous adipose tissue (ASAT) and coronary atherosclerosis in people with psoriasis.
  • It involved 232 participants undergoing imaging tests to measure their fat tissue and assess heart disease risk, revealing different correlations between ASAT and inflammation or cholesterol levels based on sex.
  • Results showed that in men, higher ASAT was linked to lower coronary atherosclerosis risk, while no significant relationship was found for women, indicating the need for further research on how ASAT interacts with chronic inflammation in different sexes.

Article Abstract

Objective: Understand the relationship between abdominal subcutaneous adipose tissue (ASAT) and coronary atherosclerosis defined as noncalcified and lipid-rich necrotic core burden in psoriasis.

Methods: We performed a cross-sectional study of 232 participants (92 women) with psoriasis and without known cardiovascular disease. Participants underwent coronary computed tomography angiography to characterize coronary atherosclerosis burden and low dose abdominal computed tomography to quantify subcutaneous and visceral adipose tissue. Fat depot volumes were first adjusted for each participant's BMI (ASAT).

Results: In women, there was a positive correlation between ASAT and systemic inflammation as assessed by hs-C-reactive protein (r=0.30; p=.004) and GlycA (r=0.29; p=.007) as well as total cholesterol (r=0.24; p=.02) and low-density lipoprotein cholesterol (r=0.22; p=.04). In men, ASAT correlated with hs-C-reactive protein (r=0.18; p=.04) and insulin resistance (r=0.17; p=.04). In models fully adjusted for traditional cardiovascular risk factors, ASAT negatively associated with noncalcified and lipid-rich necrotic core burden in men (β= -0.17; p=.03, β= -0.20; p=.03, respectively), but not women (β= -0.06; p=.57, β= 0.09; p=.49, respectively) with psoriasis.

Conclusions: For a given BMI, ASAT negatively associated with coronary atherosclerosis burden in male participants with psoriasis. The observed sex-specific effects warrant further study of ASAT in states of chronic inflammation.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8441148PMC
http://dx.doi.org/10.1016/j.ajpc.2021.100231DOI Listing

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