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Published on: October 12, 2017
Effect of Sex on Coronary Endothelial Dysfunction in People Living With HIV
Anum S Minhas1, Thorsten M Leucker1, Erin Goerlich1
1Division of Cardiology, Department of Medicine Johns Hopkins University School of Medicine Baltimore MD.
Insights
Coronary endothelial dysfunction is common in women with HIV, comparable to men. Higher PCSK9 levels in women with HIV are linked to impaired endothelial function, suggesting potential therapeutic targets.
Area of Science:
- Cardiovascular Research
- HIV Medicine
- Endocrinology
Background:
- Impaired coronary endothelial function (CEF) is a predictor of cardiovascular events and is prevalent in people living with HIV (PLWH).
- Women with HIV experience worse cardiovascular outcomes than men, yet prior studies on CEF have included limited female participants.
- Investigating sex differences in CEF and PCSK9 (proprotein convertase subtilisin/kexin type 9), a proinflammatory biomarker, is crucial for understanding cardiovascular risk in PLWH.
Purpose of the Study:
- To compare CEF in women with HIV versus those without HIV.
- To examine sex differences in CEF and serum PCSK9 levels among PLWH.
- To evaluate the association between elevated serum PCSK9 levels and impaired CEF in PLWH.
Main Methods:
- Magnetic resonance imaging (MRI) was utilized to assess CEF, measuring changes in coronary cross-sectional area and blood flow during isometric handgrip exercise.
- Serum PCSK9 levels were quantified in 106 PLWH and 76 individuals without HIV.
- Statistical analyses adjusted for age, body mass index, and menopausal status.
Main Results:
- CEF was significantly reduced in women with HIV compared to women without HIV (percentage of cross-sectional area: ß -8.3, P=0.001).
- Serum PCSK9 levels were elevated in women with HIV (306 ng/mL) compared to women without HIV (180 ng/mL, P<0.001).
- No significant sex differences in CEF or PCSK9 were observed in PLWH, and elevated PCSK9 was inversely associated with CEF.
Conclusions:
- Coronary endothelial dysfunction is present in women with HIV and is comparable to that in men with HIV.
- Women with HIV exhibit higher PCSK9 levels than women without HIV, and elevated PCSK9 is linked to impaired CEF.
- Further research is warranted to explore interventions aimed at improving endothelial function in PLWH.
Abstract:
Background Impaired coronary endothelial function (CEF) predicts cardiovascular events and occurs in people living with HIV (PLWH). Women compared with men living with HIV have worse cardiovascular outcomes, but prior CEF studies included few women. The authors aimed to compare CEF in women with HIV versus without HIV, investigate sex differences in CEF and PCSK9 (proprotein convertase subtilisin/kexin type 9) (a proinflammatory biomarker), and evaluate whether increased serum levels of PCSK9 are associated with CEF in PLWH. Methods and Results Magnetic resonance imaging was performed to measure CEF (as percent change in coronary cross-sectional area and coronary blood flow during isometric handgrip exercise, an endothelial-dependent stressor) and serum PCSK9 levels were measured in 106 PLWH and 76 people without HIV. CEF was significantly reduced in women with versus without HIV (cross-sectional area change -0.5%±9.7 versus 9.5%±3.2, respectively). After adjustment for age, body mass index, and menopausal status, women with HIV still had reduced CEF (percentage of cross-sectional area: ß -8.3 [-13 to -3.6], P=0.001) compared with women without HIV. PCSK9 was elevated in women living with HIV versus without (306 ng/mL [200-412 ng/mL] versus 180 ng/mL [154-223 ng/mL], P<0.001), and no sex differences in either CEF or PCSK9 were detected in PLWH. Elevated PCSK9 was associated with impaired CEF in PLWH; however, no significant sex differences in the association were detected. Conclusions Among PLWH, coronary endothelial dysfunction is present in women and comparable to men. PCSK9 is higher in women with versus without HIV and a significant inverse relationship between PCSK9 and CEF was shown. Future studies should determine whether PLWH would benefit from interventions to improve endothelial function.
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