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Association of pro-inflammatory high-density lipoprotein cholesterol with clinical and laboratory variables in sickle cell disease

  • Kenneth I. Ataga(corresponding author)
    ,
  • Alan Hinderliter
    ,
  • Julia Elizabeth Brittain
    ,
  • Susan Jones
    ,
  • Hao Xu
    ,
  • Jianwen Cai
*Corresponding author for this work
Scholary Output:
Contribution to journal
Article
Peer-review

Open access

Abstract

Background: Although cholesterol levels are known to be decreased in sickle cell disease (SCD), the level of pro-inflammatory high-density lipoprotein cholesterol (proHDL) and its association with clinical complications and laboratory variables has not been evaluated. Design and methods: Plasma levels of total cholesterol, high-density lipoprotein cholesterol (HDL), proHDL, and selected clinical and laboratory variables were ascertained in a cohort of SCD patients and healthy African American control subjects in this single-center, cross-sectional study. Results: Although total cholesterol was significantly lower in SCD patients compared with control subjects, HDL and proHDL levels were similar in both the SCD and control groups. In univariate analyses, proHDL was correlated with echocardiography-derived tricuspid regurgitant jet velocity. ProHDL was higher in SCD patients with suspected pulmonary hypertension (PHT) compared to patients without suspected PHT. ProHDL was positively correlated with lactate dehydrogenase, total bilirubin, direct bilirubin, indirect bilirubin, prothrombin fragment 1+2, D-dimer, and thrombin–antithrombin complexes. In multivariable analyses, only higher lactate dehydrogenase and direct bilirubin levels were associated with higher levels of proHDL. Conclusions: SCD is characterized by hypocholesterolemia. Although proHDL is not increased in SCD patients compared with healthy controls, it is significantly associated with markers of liver disease. In addition, proHDL is associated with tricuspid regurgitant jet velocity and markers of coagulation, although these associations are not significant in multivariable analyses.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 289-296 (8 pages)

Journal (Volume, Issue Number)

Hematology (Volume 20, Issue 5)

Publication milestones

  • Published - 2015

Publication status

Published - 2015

ISSN

1024-5332

Publication IDs

  • Scopus: 84929146687
  • PubMed: 24801127

Publication metrics

Metrics

SciVal
FWCI
0.58
SciVal
Author count
9
SciVal
citations
8
SciVal
Paper percentile
64
Fractional count
1
Fractional count
0.11
Fractional count
8
Fractional count
0.89
Fractional count
1
Fractional count
1
Scopus
citations

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Captures
35
Citation count
11
Social media
14854

Funding Details

FundersFunding numbers
NIH
UL1TR001111, UL1RR025747
NHLBI
U01HL117659