TY - JOUR
T1 - Plasma metabolomic study in perinatally HIV-infected children using 1H NMR spectroscopy reveals perturbed metabolites that sustain during therapy
AU - Urvinder Kaur, S.
AU - Oyeyemi, Bolaji Fatai
AU - Shet, Anita
AU - Gopalan, Bindu Parachalil
AU - Himanshu, D.
AU - Bhavesh, Neel Sarovar
AU - Tandon, Ravi
N1 - Funding Information:
We would like to acknowledge Science and Engineering Research Board-Department of Science and Technology (SERB-DST) grant ECR/ 2015/000304 (R.T.), UPOE-II Project ID: 15 (R.T.), DST PURSE II (DST/SR/PURSE Phase II/I), DBT (BT/PR23862/MED/29/1234/2017) for providing financial support to carry out research work. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. We would like to thank ICGEN Core Funds and DBT for NMR facility at ICGEB, New Delhi, India. U.K. is thankful to DBT-SRF fellowship and also Fogarty International Center (FIC) of the National Institutes of Health and the National Institute Of Diabetes And Digestive And Kidney Diseases (NIDDK) under grant #3D43TW009345-08S1 awarded to the Northern Pacific Global Health Fellows Program for support. B.F.O thank ICGEB for the award of Arturo Falaschi ICGEB pre-doctoral fellowship. R.T. is thankful to UGC-Faculty Recharge Programme (FRP).
Publisher Copyright:
© 2020 Kaur S. et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
PY - 2020/8
Y1 - 2020/8
N2 - Background Perinatally HIV-infected children on anti-retroviral treatment (ART) are reported to have metabolic abnormalities such as dyslipidemia, lipodystrophy, and insulin resistance which potentially increase the risk of diabetes, kidney, liver and cardiovascular disease. Objective To elucidate HIV-mediated metabolic complications that sustain even during ART in perinatally HIV-infected children. Method We have carried out metabolic profiling of the plasma of treatment-naïve and ART-suppressed perinatally HIV-infected children and uninfected controls using 1H nuclear magnetic resonance (NMR) spectroscopy followed by statistical analysis and annotation. Result Validated multivariate analysis showed clear distinction among our study groups. Our results showed elevated levels of lactate, glucose, phosphoenolpyruvic acid, propionic acid, 2-ketobutyric acid and tricarboxylic acid (TCA) cycle metabolites in untreated HIV-infected children compared to uninfected controls. ART normalized the levels of several metabolites, however the level of lactate, phosphoenolpyruvic acid, oxoglutaric acid, oxaloacetic acid, myoinositol and glutamine remained upregulated despite ART in HIV-infected children. Pathway analysis revealed perturbed propanoate metabolism, amino acid metabolism, glycolysis and TCA cycle in untreated and ART-suppressed HIV-infected children. Conclusion Developing therapeutic strategies targeting metabolic abnormalities may be beneficial for preventing diabetes, cardiovascular disease or other associated complications in perinatally HIV-infected children.
AB - Background Perinatally HIV-infected children on anti-retroviral treatment (ART) are reported to have metabolic abnormalities such as dyslipidemia, lipodystrophy, and insulin resistance which potentially increase the risk of diabetes, kidney, liver and cardiovascular disease. Objective To elucidate HIV-mediated metabolic complications that sustain even during ART in perinatally HIV-infected children. Method We have carried out metabolic profiling of the plasma of treatment-naïve and ART-suppressed perinatally HIV-infected children and uninfected controls using 1H nuclear magnetic resonance (NMR) spectroscopy followed by statistical analysis and annotation. Result Validated multivariate analysis showed clear distinction among our study groups. Our results showed elevated levels of lactate, glucose, phosphoenolpyruvic acid, propionic acid, 2-ketobutyric acid and tricarboxylic acid (TCA) cycle metabolites in untreated HIV-infected children compared to uninfected controls. ART normalized the levels of several metabolites, however the level of lactate, phosphoenolpyruvic acid, oxoglutaric acid, oxaloacetic acid, myoinositol and glutamine remained upregulated despite ART in HIV-infected children. Pathway analysis revealed perturbed propanoate metabolism, amino acid metabolism, glycolysis and TCA cycle in untreated and ART-suppressed HIV-infected children. Conclusion Developing therapeutic strategies targeting metabolic abnormalities may be beneficial for preventing diabetes, cardiovascular disease or other associated complications in perinatally HIV-infected children.
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U2 - 10.1371/journal.pone.0238316
DO - 10.1371/journal.pone.0238316
M3 - Article
C2 - 32866201
AN - SCOPUS:85090108602
SN - 1932-6203
VL - 15
JO - PloS one
JF - PloS one
IS - 8 august
M1 - e0238316
ER -