Publication: Factors associated with the incidence of type 2 diabetes mellitus in HIV-infected participants in the Swiss HIV Cohort Study
cris.virtual.author-orcid | 0000-0002-1375-3146 | |
cris.virtual.author-orcid | 0000-0001-7462-5132 | |
cris.virtualsource.author-orcid | 174f1323-7162-433b-b035-614cbab79f1c | |
cris.virtualsource.author-orcid | a47a659b-5a23-43fa-86e3-f9401108114c | |
datacite.rights | open.access | |
dc.contributor.author | Ledergerber, B | |
dc.contributor.author | Furrer, Hansjakob | |
dc.contributor.author | Rickenbach, M | |
dc.contributor.author | Lehmann, R | |
dc.contributor.author | Elzi, L | |
dc.contributor.author | Hirschel, B | |
dc.contributor.author | Cavassini, M | |
dc.contributor.author | Bernasconi, E | |
dc.contributor.author | Schmid, P | |
dc.contributor.author | Egger, Matthias | |
dc.contributor.author | Weber, R | |
dc.contributor.author | Swiss, HIV Cohort Study | |
dc.date.accessioned | 2024-10-13T17:17:05Z | |
dc.date.available | 2024-10-13T17:17:05Z | |
dc.date.issued | 2007 | |
dc.description.abstract | BACKGROUND: Human immunodeficiency virus (HIV)-infected persons may be at increased risk for developing type 2 diabetes mellitus because of viral coinfection and adverse effects of treatment. METHODS: We studied associations of new-onset diabetes mellitus with hepatitis B virus and hepatitis C virus coinfections and antiretroviral therapy in participants in the Swiss HIV Cohort Study, using Poisson regression. RESULTS: A total of 123 of 6513 persons experienced diabetes mellitus during 27,798 person-years of follow-up (PYFU), resulting in an incidence of 4.4 cases per 1000 PYFU (95% confidence interval [CI], 3.7-5.3 cases per 1000 PYFU). An increased incidence rate ratio (IRR) was found for male subjects (IRR, 2.5; 95% CI, 1.5-4.2), older age (IRR for subjects >60 years old, 4.3; 95% CI, 2.3-8.2), black (IRR, 2.1; 95% CI, 1.1-4.0) and Asian (IRR, 4.9; 95% CI, 2.2-10.9) ethnicity, Centers for Disease Control and Prevention disease stage C (IRR, 1.6; 95% CI, 1.04-2.4), and obesity (IRR, 4.7; 95% CI, 3.1-7.0), but results for hepatitis C virus infection or active hepatitis B virus infection were inconclusive. Strong associations were found for current treatment with nucleoside reverse-transcriptase inhibitors (IRR, 2.22; 95% CI, 1.11-4.45), nucleoside reverse-transcriptase inhibitors plus protease inhibitors (IRR, 2.48; 95% CI, 1.42-4.31), and nucleoside reverse-transcriptase inhibitors plus protease inhibitors and nonnucleoside reverse-transcriptase inhibitors (IRR, 3.25; 95% CI, 1.59-6.67) but were not found for treatment with nucleoside reverse-transcriptase inhibitors plus nonnucleoside reverse-transcriptase inhibitors (IRR, 1.47; 95% CI, 0.77-2.82). CONCLUSIONS: In addition to traditional risk factors, current treatment with protease inhibitor- and nucleoside reverse-transcriptase inhibitor-containing regimens was associated with the risk of developing type 2 diabetes mellitus. Our study did not find a significant association between viral hepatitis infection and risk of incident diabetes. | |
dc.description.numberOfPages | 9 | |
dc.description.sponsorship | Universitätsklinik für Infektiologie | |
dc.description.sponsorship | Institut für Sozial- und Präventivmedizin (ISPM) | |
dc.identifier.doi | 10.7892/boris.22117 | |
dc.identifier.isi | 000247029700020 | |
dc.identifier.pmid | 17554711 | |
dc.identifier.publisherDOI | 10.1086/518619 | |
dc.identifier.uri | https://boris-portal.unibe.ch/handle/20.500.12422/95817 | |
dc.language.iso | en | |
dc.publisher | The University of Chicago Press | |
dc.publisher.place | Cary, N.C. | |
dc.relation.isbn | 17554711 | |
dc.relation.ispartof | Clinical infectious diseases | |
dc.relation.issn | 1058-4838 | |
dc.relation.organization | DCD5A442BB13E17DE0405C82790C4DE2 | |
dc.relation.organization | DCD5A442BECFE17DE0405C82790C4DE2 | |
dc.subject.ddc | 600 - Technology::610 - Medicine & health | |
dc.title | Factors associated with the incidence of type 2 diabetes mellitus in HIV-infected participants in the Swiss HIV Cohort Study | |
dc.type | article | |
dspace.entity.type | Publication | |
dspace.file.type | text | |
oaire.citation.endPage | 9 | |
oaire.citation.issue | 1 | |
oaire.citation.startPage | 111 | |
oaire.citation.volume | 45 | |
oairecerif.author.affiliation | Universitätsklinik für Infektiologie | |
oairecerif.author.affiliation | Institut für Sozial- und Präventivmedizin (ISPM) | |
unibe.contributor.role | creator | |
unibe.contributor.role | creator | |
unibe.contributor.role | creator | |
unibe.contributor.role | creator | |
unibe.contributor.role | creator | |
unibe.contributor.role | creator | |
unibe.contributor.role | creator | |
unibe.contributor.role | creator | |
unibe.contributor.role | creator | |
unibe.contributor.role | creator | |
unibe.contributor.role | creator | |
unibe.contributor.role | creator | |
unibe.date.licenseChanged | 2019-10-23 08:31:49 | |
unibe.description.ispublished | pub | |
unibe.eprints.legacyId | 22117 | |
unibe.journal.abbrevTitle | CLIN INFECT DIS | |
unibe.refereed | true | |
unibe.subtype.article | journal |
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