Persistent metabolic changes in HIV-infected patients during the first year of combination antiretroviral therapy

The HIV-human metabolic relationship is a complex interaction convoluted even more by antiretroviral therapy (cART) and comorbidities. The ability of cART to undo the HIV induced metabolic dysregulation is unclear and under-investigated. Using targeted metabolomics and multiplex immune biomarker ana...

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Veröffentlicht in:Scientific reports Jg. 8; H. 1; S. 16947 - 11
Hauptverfasser: Peltenburg, N. Chantal, Schoeman, Johannes C., Hou, Jun, Mora, Fernando, Harms, Amy C., Lowe, Selwyn H., Bierau, Jörgen, Bakker, Jaap A., Verbon, Annelies, Hankemeier, Thomas, Boonstra, Andre
Format: Journal Article
Sprache:Englisch
Veröffentlicht: London Nature Publishing Group UK 16.11.2018
Nature Publishing Group
Schlagworte:
631/250/255/1901
631/45/320
692/53/2422
96/21
Antiretroviral agents
Antiretroviral drugs
Antiretroviral therapy
Drug therapy
HIV
Human immunodeficiency virus
Humanities and Social Sciences
Infections
IP-10 protein
Lipid metabolism
Metabolic pathways
Metabolism
Metabolomics
Monocyte chemoattractant protein 1
multidisciplinary
Phospholipids
Science
Science (multidisciplinary)
Triglycerides
Tryptophan
Triglyceride Species
HIV-associated Neurocognitive Disorders (HAND)
Paired Patient Samples
Plasmalogen Phosphatidylcholine (PC-O)
Metabolic Dysregulation
ISSN:2045-2322, 2045-2322
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Zusammenfassung:The HIV-human metabolic relationship is a complex interaction convoluted even more by antiretroviral therapy (cART) and comorbidities. The ability of cART to undo the HIV induced metabolic dysregulation is unclear and under-investigated. Using targeted metabolomics and multiplex immune biomarker analysis, we characterized plasma samples obtained from 18 untreated HIV-1-infected adult patients and compared these to a non-HIV infected (n = 23) control population. The biogenic amine perturbations during an untreated HIV infection implicated altered tryptophan- nitrogen- and muscle metabolism. Furthermore, the lipid profiles of untreated patients were also significantly altered compared to controls. In untreated HIV infection, the sphingomyelins and phospholipids correlated negatively to markers of infection IP-10 and sIL-2R whereas a strong association was found between triglycerides and MCP-1. In a second cohort, we characterized plasma samples obtained from 28 HIV-1-infected adult patients before and 12 months after the start of cART, to investigate the immune-metabolic changes associated with cART. The identified altered immune-metabolic pathways of an untreated HIV infection showed minimal change after 12 months of cART. In conclusion, 12 months of cART impacts only mildly on the metabolic dysregulation underlying an untreated HIV infection and provide insights into the comorbidities present in virally suppressed HIV patients.
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ISSN:2045-2322
2045-2322
DOI:10.1038/s41598-018-35271-0