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dc.date.accessioned2018-03-12T13:29:41Z
dc.date.available2018-03-12T13:29:41Z
dc.date.created2017-08-17T15:30:29Z
dc.date.issued2017
dc.identifier.citationHove-Skovsgaard, Malene Gaardbo, Julie Christine Kolte, Lilian Winding, Kamilla Seljeflot, Ingebjørg Svardal, Asbjørn M. Berge, Rolf Kristian Gerstoft, Jan Ullum, Henrik Trøseid, Marius Nielsen, Susanne Dam . HIV-infected persons with type 2 diabetes show evidence of endothelial dysfunction and increased inflammation. BMC Infectious Diseases. 2017, 17:234, 1-8
dc.identifier.urihttp://hdl.handle.net/10852/60913
dc.description.abstractBackground Increased incidence of cardiovascular diseases (CVD) in both HIV infection and type 2 diabetes (T2D) compared to the general population has been described. Little is known about the combined effect of HIV infection and T2D on inflammation and endothelial function, both of which may contribute to elevated risk of CVD. Methods Cross-sectional study including 50 HIV-infected persons on combination anti-retroviral therapy (cART), with HIV RNA <200 copies/mL (n = 25 with T2D (HIV + T2D+), n = 25 without T2D (HIV + T2D-)) and 50 uninfected persons (n = 22 with T2D (HIV-T2D+) and n = 28 without T2D (HIV-T2D-)). Groups were matched on age and sex. High sensitive C-reactive protein (hsCRP) was used to determine inflammation (cut-off 3 mg/L). The marker of endothelial dysfunction asymmetric dimethylarginine (ADMA) was measured using high performance liquid chromatography. Trimethylamine-N-oxide (TMAO), a microbiota-dependent, pro-atherogenic marker was measured using stable isotope dilution LC/MS/MS. Results The percentage of HIV + T2D+, HIV + T2D-, HIV-T2D+, and HIV-T2D- with hsCRP above cut-off was 50%, 19%, 47%, and 11%, respectively. HIV + T2D+ had elevated ADMA (0.67 μM (0.63-0.72) compared to HIV + T2D- (0.60 μM (0.57-0.64) p = 0.017), HIV-T2D+ (0.57 μM (0.51-63) p = 0.008), and HIV-T2D- (0.55 μM (0.52-0.58) p < 0.001). No differences in TMAO between groups were found. However, a positive correlation between ADMA and TMAO was found in the total population (rs = 0.32, p = 0.001), which was mainly driven by a close correlation in HIV + T2D+ (rs = 0.63, p = 0.001). Conclusion Elevated inflammation and evidence of endothelial dysfunction was found in HIV-infected persons with T2D. The effect on inflammation was mainly driven by T2D, while both HIV infection and T2D may contribute to endothelial dysfunction. Whether gut microbiota is a contributing factor to this remains to be determined.en_US
dc.languageEN
dc.language.isoenen_US
dc.publisherBioMed Central
dc.rightsAttribution 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.titleHIV-infected persons with type 2 diabetes show evidence of endothelial dysfunction and increased inflammationen_US
dc.typeJournal articleen_US
dc.creator.authorHove-Skovsgaard, Malene
dc.creator.authorGaardbo, Julie Christine
dc.creator.authorKolte, Lilian
dc.creator.authorWinding, Kamilla
dc.creator.authorSeljeflot, Ingebjørg
dc.creator.authorSvardal, Asbjørn M.
dc.creator.authorBerge, Rolf Kristian
dc.creator.authorGerstoft, Jan
dc.creator.authorUllum, Henrik
dc.creator.authorTrøseid, Marius
dc.creator.authorNielsen, Susanne Dam
cristin.unitcode185,53,11,10
cristin.unitnameHjertemedisinsk avdeling
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1
dc.identifier.cristin1487040
dc.identifier.bibliographiccitationinfo:ofi/fmt:kev:mtx:ctx&ctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=BMC Infectious Diseases&rft.volume=17:234&rft.spage=1&rft.date=2017
dc.identifier.jtitleBMC Infectious Diseases
dc.identifier.volume17
dc.identifier.doihttp://dx.doi.org/10.1186/s12879-017-2334-8
dc.identifier.urnURN:NBN:no-63545
dc.type.documentTidsskriftartikkelen_US
dc.type.peerreviewedPeer reviewed
dc.source.issn1471-2334
dc.identifier.fulltextFulltext https://www.duo.uio.no/bitstream/handle/10852/60913/2/Skovsgaard%2Bet%2Bal.pdf
dc.type.versionPublishedVersion
cristin.articleid234


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