Evidence map›Paper›PMID 26493269›Full record

ArticleThe neuroradiology journal2015

Differences in the variability of cerebral proton magnetic resonance spectroscopy (1H-MRS) measurements within three HIV-infected cohorts.

Shivanee Vigneswaran, Jaime H Vera Rojas, Lucy Garvey, Simon Taylor-Robinson, Alan Winston

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Article in The neuroradiology journal, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2citing papers in PubMed
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3 · Its place in the literature

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2 citing papers in PubMed.

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5 · Who and what money

Authors and funding

5 authors.

Shivanee VigneswaranImperial College London, London, UK shivanee.vigneswaran@nhs.net.
Jaime H Vera RojasDivision of medicine, Brighton and Sussex Medical School Department of HIV and GU Medicine, Imperial College Healthcare NHS Trust, London, UK.
Lucy GarveyDepartment of HIV and GU Medicine, Imperial College Healthcare NHS Trust, London, UK.
Simon Taylor-RobinsonDepartment of Medicine, Faculty of Medicine, Imperial College London, St Mary's Hospital Campus, London, UK.
Alan WinstonDepartment of HIV and GU Medicine, Imperial College Healthcare NHS Trust, London, UK.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionCerebral functional impairment remains prevalent in effectively treated HIV-infected subjects. As the results of formal cognitive testing are highly variable, surrogate markers to accurately measure cerebral function parameters are needed. Such markers include measurement of cerebral metabolite ratios (CMR) using proton magnetic resonance spectroscopy (1H-MRS). However, data on the inter-subject variability of CMR are sparse. Our aim was to assess inter-subject variability in CMRs within three different HIV-infected cohorts.

methodsCerebral 1H-MRS was performed using a Phillips Achieva™ 1.5 Tesla magnetic resonance scanner in HIV-infected subjects as follows: 12 subjects before (group 1) and after intensification of antiretroviral therapy with maraviroc (group 2) and 13 subjects with acute viral hepatitis C (HCV) co-infection (group 3). The coefficients of variation (CV) for CMRs in each group were determined and compared using non-parametric tests to determine whether the inter-subject variability differed significantly. All baseline characteristics between the groups were similar.

resultsOverall CVs for all CMRs in groups 1, 2 and 3 were 32.3%, 33.2% and 23.4%, respectively (group 1 vs. 2, p=0.863; group 1 vs. 3, p=0.076). On testing for differences in variability between individual CMRs, two metabolites in the right basal ganglia (RBG) had statistically significantly different CVs when comparing group 1 with group 3: N-acetyl aspartate/creatine (NAA/Cr), p=0.029 and myo-Inositol/creatine (mI/Cr), p=0.016.

conclusionThe variability of 1H MRS-measurable CMRs in HIV-infected individuals was lower in those with acute HCV co-infection (group 3).We can conclude that the use of these CMRs in 1H MRS imaging in patients with HIV/acute HCV co-infection is more reliable to assess cerebral function than in patients with HIV infection alone. This has implications for future sample size estimations.

Indexed as

Brain ChemistryAdultAntiretroviral Therapy, Highly ActiveAspartic AcidBasal GangliaBrainCohort StudiesCreatineCyclohexanesFemaleHepatitis CHIV Fusion InhibitorsHIV InfectionsHumansInositolMagnetic Resonance ImagingAspartic AcidCreatineCyclohexanesHIV Fusion InhibitorsInositolMaravirocN-acetylaspartateProtonsTriazoles1H MRSacute HCVco-infectionHIVvariability

Identifiers

PMID26493269
PMCPMC4757133

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