Source:http://linkedlifedata.com/resource/pubmed/id/18073016
Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
12
|
pubmed:dateCreated |
2007-12-12
|
pubmed:abstractText |
Non-nucleoside reverse transcriptase inhibitors (NNRTIs) have a longer half-life than nucleoside reverse transcriptase inhibitor (NRTIs). Simultaneous interruption of all drugs exposes the patients to NNRTI monotherapy. This study evaluated HIV-1 genotype after treatment interruption (TI) of NNRTI-based antiretroviral therapy (ART) and virological response after resumption of the same ART regimen. A prospective study was conducted in HIV-1-infected patients who enrolled into a CD4-guided TI study. All patients continued dual NRTIs for a further 7-10 days at NNRTI TI. HIV-1 genotypic assay was performed prior to resumption of the same ART regimen. Forty-three patients required ART resumption after TI from NNRTI-based regimens. Mean age was 42.7 years; 44% were men. Median CD4 and HIV-1 RNA at the time of ART resumption were 178 cell/mm(3) and 5.78 log copies/mL, respectively. HIV-1 genotype revealed no mutations contributed to NRTI or NNRTI resistance. Of all, 56% and 100% patients achieved undetectable HIV-1 RNA at three and six months, respectively. Median CD4 were 386 and 419 cells/mm(3) at the corresponding periods. In conclusion, continuation of dual NRTIs for 7-10 days after TI of NNRTI-based regimens can minimize the risk of acquired NNRTI resistance. With this strategy, the same regimen can be used for resumption and also yield good virological and immunological outcomes.
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Anti-HIV Agents,
http://linkedlifedata.com/resource/pubmed/chemical/HIV Reverse Transcriptase,
http://linkedlifedata.com/resource/pubmed/chemical/RNA, Viral,
http://linkedlifedata.com/resource/pubmed/chemical/Reverse Transcriptase Inhibitors,
http://linkedlifedata.com/resource/pubmed/chemical/reverse transcriptase, Human...
|
pubmed:status |
MEDLINE
|
pubmed:month |
Dec
|
pubmed:issn |
0956-4624
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
18
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
832-4
|
pubmed:meshHeading |
pubmed-meshheading:18073016-Adult,
pubmed-meshheading:18073016-Anti-HIV Agents,
pubmed-meshheading:18073016-CD4 Lymphocyte Count,
pubmed-meshheading:18073016-Drug Administration Schedule,
pubmed-meshheading:18073016-Drug Therapy, Combination,
pubmed-meshheading:18073016-Female,
pubmed-meshheading:18073016-HIV Infections,
pubmed-meshheading:18073016-HIV Reverse Transcriptase,
pubmed-meshheading:18073016-HIV-1,
pubmed-meshheading:18073016-Humans,
pubmed-meshheading:18073016-Male,
pubmed-meshheading:18073016-Middle Aged,
pubmed-meshheading:18073016-RNA, Viral,
pubmed-meshheading:18073016-Reverse Transcriptase Inhibitors,
pubmed-meshheading:18073016-Treatment Outcome,
pubmed-meshheading:18073016-Viral Load
|
pubmed:year |
2007
|
pubmed:articleTitle |
HIV-1 genotype after interruption of non-nucleoside reverse transcriptase inhibitor-based antiretroviral therapy and virological response after resumption of the same regimen.
|
pubmed:affiliation |
Faculty of Medicine, Ramathibodi Hospital, Mahidol University, Bangkok, Thailand. ssungkanuparph@yahoo.com
|
pubmed:publicationType |
Journal Article,
Clinical Trial,
Research Support, Non-U.S. Gov't
|