Skip to main content
Journal cover image

HIV and Hepatitis C-Coinfected Patients Have Lower Low-Density Lipoprotein Cholesterol Despite Higher Proprotein Convertase Subtilisin Kexin 9 (PCSK9): An Apparent "PCSK9-Lipid Paradox".

Publication ,  Journal Article
Kohli, P; Ganz, P; Ma, Y; Scherzer, R; Hur, S; Weigel, B; Grunfeld, C; Deeks, S; Wasserman, S; Scott, R; Hsue, PY
Published in: J Am Heart Assoc
April 29, 2016

BACKGROUND: Proprotein convertase subtilisin kexin 9 (PCSK9) inhibitors reduce low-density lipoprotein cholesterol (LDL-C) and improve outcomes in the general population. HIV-infected individuals are at increased risk for cardiovascular events and have high rates of dyslipidemia and hepatitis C virus (HCV) coinfection, making PCSK9 inhibition a potentially attractive therapy. METHODS AND RESULTS: We studied 567 participants from a clinic-based cohort to compare PCSK9 levels in patients with HIV/HCV coinfection (n=110) with those with HIV infection alone (n=385) and with uninfected controls (n=72). The mean age was 49 years, and the median LDL-C level was 100 mg/dL (IQR 77-124 mg/dL); 21% were taking statins. The 3 groups had similar rates of traditional risk factors. Total cholesterol, LDL-C, and high-density lipoprotein cholesterol levels were lower in coinfected patients compared with controls (P<0.001). PCSK9 was 21% higher in HIV/HCV-coinfected patients versus controls (95% CI 9-34%, P<0.001) and 11% higher in coinfected individuals versus those with HIV infection alone (95% CI 3-20%, P=0.008). After adjustment for cardiovascular risk factors, HIV/HCV coinfection remained significantly associated with 20% higher PCSK9 levels versus controls (95% CI 8-33%, P=0.001). Interleukin-6 levels increased in a stepwise fashion from controls (lowest) to HIV-infected to HIV/HCV-coinfected individuals (highest) and correlated with PCSK9 (r=0.11, P=0.018). CONCLUSIONS: Despite having lower LDL-C, circulating PCSK9 levels were increased in patients coinfected with HIV and HCV in parallel with elevations in the inflammatory, proatherogenic cytokine interleukin-6. Clinical trials should be conducted to determine the efficacy of targeted PCSK9 inhibition in the setting of HIV/HCV coinfection.

Duke Scholars

Altmetric Attention Stats
Dimensions Citation Stats

Published In

J Am Heart Assoc

DOI

EISSN

2047-9980

Publication Date

April 29, 2016

Volume

5

Issue

5

Location

England

Related Subject Headings

  • Proprotein Convertase 9
  • Middle Aged
  • Male
  • Interleukin-6
  • Hydroxymethylglutaryl-CoA Reductase Inhibitors
  • Humans
  • Hepatitis C, Chronic
  • HIV Infections
  • Female
  • Dyslipidemias
 

Citation

APA
Chicago
ICMJE
MLA
NLM
Kohli, P., Ganz, P., Ma, Y., Scherzer, R., Hur, S., Weigel, B., … Hsue, P. Y. (2016). HIV and Hepatitis C-Coinfected Patients Have Lower Low-Density Lipoprotein Cholesterol Despite Higher Proprotein Convertase Subtilisin Kexin 9 (PCSK9): An Apparent "PCSK9-Lipid Paradox". J Am Heart Assoc, 5(5). https://doi.org/10.1161/JAHA.115.002683
Kohli, Payal, Peter Ganz, Yifei Ma, Rebecca Scherzer, Sophia Hur, Bernard Weigel, Carl Grunfeld, et al. “HIV and Hepatitis C-Coinfected Patients Have Lower Low-Density Lipoprotein Cholesterol Despite Higher Proprotein Convertase Subtilisin Kexin 9 (PCSK9): An Apparent "PCSK9-Lipid Paradox".J Am Heart Assoc 5, no. 5 (April 29, 2016). https://doi.org/10.1161/JAHA.115.002683.
Kohli P, Ganz P, Ma Y, Scherzer R, Hur S, Weigel B, Grunfeld C, Deeks S, Wasserman S, Scott R, Hsue PY. HIV and Hepatitis C-Coinfected Patients Have Lower Low-Density Lipoprotein Cholesterol Despite Higher Proprotein Convertase Subtilisin Kexin 9 (PCSK9): An Apparent "PCSK9-Lipid Paradox". J Am Heart Assoc. 2016 Apr 29;5(5).
Journal cover image

Published In

J Am Heart Assoc

DOI

EISSN

2047-9980

Publication Date

April 29, 2016

Volume

5

Issue

5

Location

England

Related Subject Headings

  • Proprotein Convertase 9
  • Middle Aged
  • Male
  • Interleukin-6
  • Hydroxymethylglutaryl-CoA Reductase Inhibitors
  • Humans
  • Hepatitis C, Chronic
  • HIV Infections
  • Female
  • Dyslipidemias