Association of microbial translocation biomarkers with clinical outcome in controllers HIV-infected patients. (27th March 2015)
- Record Type:
- Journal Article
- Title:
- Association of microbial translocation biomarkers with clinical outcome in controllers HIV-infected patients. (27th March 2015)
- Main Title:
- Association of microbial translocation biomarkers with clinical outcome in controllers HIV-infected patients
- Authors:
- León, Agathe
Leal, Lorna
Torres, Berta
Lucero, Constanza
Inciarte, Alexy
Arnedo, Mireia
Plana, Montserrat
Vila, Jordi
Gatell, Josep M.
García, Felipe - Abstract:
- <abstract> <title> <x xml:space="preserve">Abstract</x> </title> <sec> <title>Background:</title> <p>A proportion of patients who spontaneously control viral load (controllers) experienced clinical progression. We hypothesized that microbial translocation would independently determine the rate of disease progression in controllers.</p> </sec> <sec> <title>Methods:</title> <p>sCD14, lipopolysaccharide-binding protein (LBP) and EndoCab levels were assessed in 114 antiretroviral-naive patients with CD4<sup>+</sup> T cells above 500 cells/μl (including 63 controllers and 51 noncontrollers). The independent predictive value of these markers on time to progression to the combined endpoint of AIDS, non-AIDS event, initiation of combination antiretroviral therapy (cART) or CD4<sup>+</sup> cell count less than 500 cells/μl was assessed using a Cox regression model.</p> </sec> <sec> <title>Results:</title> <p>Most of the patients progressed to a combined endpoint (60%). Clinical progression in controllers was significantly lower than in noncontrollers (<italic>P</italic> = 0.02). Controllers with lower than the median baseline CD4<sup>+</sup> T-cell count and higher than the median baseline viral load, sCD14 and EndoCab levels had a worse prognosis (<italic>P</italic> &lt; 0.0001, <italic>P</italic> = 0.007, <italic>P</italic> = 0.05 and <italic>P</italic> = 0.012), while noncontrollers with higher than the median baseline LBP level also had a worse prognosis<abstract> <title> <x xml:space="preserve">Abstract</x> </title> <sec> <title>Background:</title> <p>A proportion of patients who spontaneously control viral load (controllers) experienced clinical progression. We hypothesized that microbial translocation would independently determine the rate of disease progression in controllers.</p> </sec> <sec> <title>Methods:</title> <p>sCD14, lipopolysaccharide-binding protein (LBP) and EndoCab levels were assessed in 114 antiretroviral-naive patients with CD4<sup>+</sup> T cells above 500 cells/μl (including 63 controllers and 51 noncontrollers). The independent predictive value of these markers on time to progression to the combined endpoint of AIDS, non-AIDS event, initiation of combination antiretroviral therapy (cART) or CD4<sup>+</sup> cell count less than 500 cells/μl was assessed using a Cox regression model.</p> </sec> <sec> <title>Results:</title> <p>Most of the patients progressed to a combined endpoint (60%). Clinical progression in controllers was significantly lower than in noncontrollers (<italic>P</italic> = 0.02). Controllers with lower than the median baseline CD4<sup>+</sup> T-cell count and higher than the median baseline viral load, sCD14 and EndoCab levels had a worse prognosis (<italic>P</italic> &lt; 0.0001, <italic>P</italic> = 0.007, <italic>P</italic> = 0.05 and <italic>P</italic> = 0.012), while noncontrollers with higher than the median baseline LBP level also had a worse prognosis (<italic>P</italic> = 0.019). sCD14 and LBP increased and EndoCab decreased over time [from baseline (median values: 1486, 17604 ng/ml and 68 MMU/ml, respectively, to the date of event or the last determination (median values: 1663, 20230 ng/ml and 49 MMU/ml), respectively] in controllers (<italic>P</italic> = 0.04, 0.08 and 0.0006, respectively).</p> </sec> <sec> <title>Conclusion:</title> <p>Microbial translocation seems to be an important determinant of clinical progression in HIV-infected controllers independently of viremia. Measures to improve the intestinal mucosa damage or decrease translocation could influence the outcome in these patients.</p> </sec> </abstract> … (more)
- Is Part Of:
- AIDS. Volume 29:Number 6(2015)
- Journal:
- AIDS
- Issue:
- Volume 29:Number 6(2015)
- Issue Display:
- Volume 29, Issue 6 (2015)
- Year:
- 2015
- Volume:
- 29
- Issue:
- 6
- Issue Sort Value:
- 2015-0029-0006-0000
- Page Start:
- Page End:
- Publication Date:
- 2015-03-27
- Subjects:
- AIDS (Disease) -- Periodicals
Acquired Immunodeficiency Syndrome
AIDS (Disease)
Periodicals
Periodicals
616.9792005 - Journal URLs:
- http://gateway.ovid.com/ovidweb.cgi?T=JS&MODE=ovid&PAGE=toc&D=ovft&AN=00002030-000000000-00000 ↗
http://journals.lww.com/aidsonline/pages/default.aspx?desktopMode=true ↗
http://journals.lww.com/pages/default.aspx ↗ - DOI:
- 10.1097/QAD.0000000000000596 ↗
- Languages:
- English
- ISSNs:
- 0269-9370
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 0773.083000
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British Library STI - ELD Digital store - Ingest File:
- 3256.xml