Low prevalence of insulin resistance among HIV-infected children receiving nonnucleoside reverse transcriptase inhibitor-based highly active antiretroviral therapy in Thailand

Background: Highly active antiretroviral therapy (HAART) is reported to cause insulin resistance among adults, but effects on children are less clear. We attempted to describe the prevalence of insulin resistance among HIV-infected children receiving HAART. Methods: Insulin resistance was assessed a...

Full description

Saved in:
Bibliographic Details
Main Authors: Lee B., Aurpibul L., Sirisanthana V., Mangklabruks A., Sirisanthana T., Puthanakit T.
Format: Article
Language:English
Published: 2014
Online Access:http://www.scopus.com/inward/record.url?eid=2-s2.0-68949102262&partnerID=40&md5=fcfc64aed0114a973ac0f500b287d031
http://cmuir.cmu.ac.th/handle/6653943832/2809
Tags: Add Tag
No Tags, Be the first to tag this record!
Institution: Chiang Mai University
Language: English
id th-cmuir.6653943832-2809
record_format dspace
spelling th-cmuir.6653943832-28092014-08-30T02:25:25Z Low prevalence of insulin resistance among HIV-infected children receiving nonnucleoside reverse transcriptase inhibitor-based highly active antiretroviral therapy in Thailand Lee B. Aurpibul L. Sirisanthana V. Mangklabruks A. Sirisanthana T. Puthanakit T. Background: Highly active antiretroviral therapy (HAART) is reported to cause insulin resistance among adults, but effects on children are less clear. We attempted to describe the prevalence of insulin resistance among HIV-infected children receiving HAART. Methods: Insulin resistance was assessed at 96 weeks of treatment with nonnucleoside reverse transcriptase inhibitor (NNRTI)-based HAART (nevirapine or efavirenz with stavudine and lamivudine) among children in Chiang Mai, Thailand. Insulin resistance was defined as homeostasis model assessment for insulin resistance (HOMA-IR) ≥ 3.16, fasting c-peptide ≥ 4.40ng/mL or fasting insulin ≥ 25.0μU/mL. Impaired fasting glucose (IFG) was defined as glucose ≥110mg/dL. Measurements were analysed for associations with age, lipodystrophy, treatment regimen and clinical data. Results: The prevalence of insulin resistance was 6.5% no child had IFG. Those with insulin resistance were older with higher body mass index. Children ≥ 10 years had higher HOMA-IR, c-peptide and insulin, but no difference was seen in the frequency of insulin resistance. No associations between insulin resistance and lipodystrophy or treatment regimen were detected. Conclusions: Insulin resistance is uncommon among children receiving NNRTI-based HAART and is unrelated to lipodystrophy. © 2009 British HIV Association. 2014-08-30T02:25:25Z 2014-08-30T02:25:25Z 2009 Article 14642662 10.1111/j.1468-1293.2008.00653.x 19018877 HMIEA http://www.scopus.com/inward/record.url?eid=2-s2.0-68949102262&partnerID=40&md5=fcfc64aed0114a973ac0f500b287d031 http://cmuir.cmu.ac.th/handle/6653943832/2809 English
institution Chiang Mai University
building Chiang Mai University Library
country Thailand
collection CMU Intellectual Repository
language English
description Background: Highly active antiretroviral therapy (HAART) is reported to cause insulin resistance among adults, but effects on children are less clear. We attempted to describe the prevalence of insulin resistance among HIV-infected children receiving HAART. Methods: Insulin resistance was assessed at 96 weeks of treatment with nonnucleoside reverse transcriptase inhibitor (NNRTI)-based HAART (nevirapine or efavirenz with stavudine and lamivudine) among children in Chiang Mai, Thailand. Insulin resistance was defined as homeostasis model assessment for insulin resistance (HOMA-IR) ≥ 3.16, fasting c-peptide ≥ 4.40ng/mL or fasting insulin ≥ 25.0μU/mL. Impaired fasting glucose (IFG) was defined as glucose ≥110mg/dL. Measurements were analysed for associations with age, lipodystrophy, treatment regimen and clinical data. Results: The prevalence of insulin resistance was 6.5% no child had IFG. Those with insulin resistance were older with higher body mass index. Children ≥ 10 years had higher HOMA-IR, c-peptide and insulin, but no difference was seen in the frequency of insulin resistance. No associations between insulin resistance and lipodystrophy or treatment regimen were detected. Conclusions: Insulin resistance is uncommon among children receiving NNRTI-based HAART and is unrelated to lipodystrophy. © 2009 British HIV Association.
format Article
author Lee B.
Aurpibul L.
Sirisanthana V.
Mangklabruks A.
Sirisanthana T.
Puthanakit T.
spellingShingle Lee B.
Aurpibul L.
Sirisanthana V.
Mangklabruks A.
Sirisanthana T.
Puthanakit T.
Low prevalence of insulin resistance among HIV-infected children receiving nonnucleoside reverse transcriptase inhibitor-based highly active antiretroviral therapy in Thailand
author_facet Lee B.
Aurpibul L.
Sirisanthana V.
Mangklabruks A.
Sirisanthana T.
Puthanakit T.
author_sort Lee B.
title Low prevalence of insulin resistance among HIV-infected children receiving nonnucleoside reverse transcriptase inhibitor-based highly active antiretroviral therapy in Thailand
title_short Low prevalence of insulin resistance among HIV-infected children receiving nonnucleoside reverse transcriptase inhibitor-based highly active antiretroviral therapy in Thailand
title_full Low prevalence of insulin resistance among HIV-infected children receiving nonnucleoside reverse transcriptase inhibitor-based highly active antiretroviral therapy in Thailand
title_fullStr Low prevalence of insulin resistance among HIV-infected children receiving nonnucleoside reverse transcriptase inhibitor-based highly active antiretroviral therapy in Thailand
title_full_unstemmed Low prevalence of insulin resistance among HIV-infected children receiving nonnucleoside reverse transcriptase inhibitor-based highly active antiretroviral therapy in Thailand
title_sort low prevalence of insulin resistance among hiv-infected children receiving nonnucleoside reverse transcriptase inhibitor-based highly active antiretroviral therapy in thailand
publishDate 2014
url http://www.scopus.com/inward/record.url?eid=2-s2.0-68949102262&partnerID=40&md5=fcfc64aed0114a973ac0f500b287d031
http://cmuir.cmu.ac.th/handle/6653943832/2809
_version_ 1681419929335627776