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Correlation between HIV disease and lipid metabolism in antiretroviral-naïve HIV-infected patients in Japan
Antiretroviral therapy alters lipid metabolism in HIV-infected patients. However, interpreting the impact of HIV infection on lipid metabolism is difficult because of various associated factors, including antiretroviral drugs and demographic characteristics. A few studies have associated HIV infecti...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Japan
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3278606/ https://www.ncbi.nlm.nih.gov/pubmed/21735099 http://dx.doi.org/10.1007/s10156-011-0275-5 |
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author | Oka, Fukuko Naito, Toshio Oike, Miki Imai, Rino Saita, Mizue Inui, Akihiro Mitsuhashi, Kazunori Isonuma, Hiroshi Shimbo, Takuro |
author_facet | Oka, Fukuko Naito, Toshio Oike, Miki Imai, Rino Saita, Mizue Inui, Akihiro Mitsuhashi, Kazunori Isonuma, Hiroshi Shimbo, Takuro |
author_sort | Oka, Fukuko |
collection | PubMed |
description | Antiretroviral therapy alters lipid metabolism in HIV-infected patients. However, interpreting the impact of HIV infection on lipid metabolism is difficult because of various associated factors, including antiretroviral drugs and demographic characteristics. A few studies have associated HIV infection with lipid metabolism in antiretroviral-naïve HIV-infected patients. Because there were no data in this regard from Japan, the present study examined the impact of HIV infection, as well as demographic and clinical features, on lipid metabolism in antiretroviral-naïve HIV-infected patients in Japan. We performed a cross-sectional study to examine the impact of HIV disease, demographic and clinical characteristics on lipid metabolism among 168 HIV-infected Japanese men who were antiretroviral naïve and who did not have hemophilia, including patients who took medication for dyslipidemia. The mean age of the patients was 45.7 years; 0.6% of the patients took medication to dyslipidemia. The mean CD4 lymphocyte count was 289/μL, the mean baseline log10 HIV viral load was 4.2 HIV-1 RNA copies/mL, and 22% of the patients had a history of AIDS-defining events. A higher HDL-C concentration was associated with a higher CD4 lymphocyte count (p = 0.043). Also, a higher LDL-C concentration was associated with a higher CD4 lymphocyte count (p = 0.003). Infection with HIV was associated with dyslipidemia in antiretroviral-naïve patients. More advanced HIV disease was associated with less favorable lipid homeostatic profiles. These results are similar to findings from other countries. |
format | Online Article Text |
id | pubmed-3278606 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Springer Japan |
record_format | MEDLINE/PubMed |
spelling | pubmed-32786062012-02-21 Correlation between HIV disease and lipid metabolism in antiretroviral-naïve HIV-infected patients in Japan Oka, Fukuko Naito, Toshio Oike, Miki Imai, Rino Saita, Mizue Inui, Akihiro Mitsuhashi, Kazunori Isonuma, Hiroshi Shimbo, Takuro J Infect Chemother Original Article Antiretroviral therapy alters lipid metabolism in HIV-infected patients. However, interpreting the impact of HIV infection on lipid metabolism is difficult because of various associated factors, including antiretroviral drugs and demographic characteristics. A few studies have associated HIV infection with lipid metabolism in antiretroviral-naïve HIV-infected patients. Because there were no data in this regard from Japan, the present study examined the impact of HIV infection, as well as demographic and clinical features, on lipid metabolism in antiretroviral-naïve HIV-infected patients in Japan. We performed a cross-sectional study to examine the impact of HIV disease, demographic and clinical characteristics on lipid metabolism among 168 HIV-infected Japanese men who were antiretroviral naïve and who did not have hemophilia, including patients who took medication for dyslipidemia. The mean age of the patients was 45.7 years; 0.6% of the patients took medication to dyslipidemia. The mean CD4 lymphocyte count was 289/μL, the mean baseline log10 HIV viral load was 4.2 HIV-1 RNA copies/mL, and 22% of the patients had a history of AIDS-defining events. A higher HDL-C concentration was associated with a higher CD4 lymphocyte count (p = 0.043). Also, a higher LDL-C concentration was associated with a higher CD4 lymphocyte count (p = 0.003). Infection with HIV was associated with dyslipidemia in antiretroviral-naïve patients. More advanced HIV disease was associated with less favorable lipid homeostatic profiles. These results are similar to findings from other countries. Springer Japan 2011-07-07 2012-02 /pmc/articles/PMC3278606/ /pubmed/21735099 http://dx.doi.org/10.1007/s10156-011-0275-5 Text en © Japanese Society of Chemotherapy and The Japanese Association for Infectious Diseases 2011 |
spellingShingle | Original Article Oka, Fukuko Naito, Toshio Oike, Miki Imai, Rino Saita, Mizue Inui, Akihiro Mitsuhashi, Kazunori Isonuma, Hiroshi Shimbo, Takuro Correlation between HIV disease and lipid metabolism in antiretroviral-naïve HIV-infected patients in Japan |
title | Correlation between HIV disease and lipid metabolism in antiretroviral-naïve HIV-infected patients in Japan |
title_full | Correlation between HIV disease and lipid metabolism in antiretroviral-naïve HIV-infected patients in Japan |
title_fullStr | Correlation between HIV disease and lipid metabolism in antiretroviral-naïve HIV-infected patients in Japan |
title_full_unstemmed | Correlation between HIV disease and lipid metabolism in antiretroviral-naïve HIV-infected patients in Japan |
title_short | Correlation between HIV disease and lipid metabolism in antiretroviral-naïve HIV-infected patients in Japan |
title_sort | correlation between hiv disease and lipid metabolism in antiretroviral-naïve hiv-infected patients in japan |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3278606/ https://www.ncbi.nlm.nih.gov/pubmed/21735099 http://dx.doi.org/10.1007/s10156-011-0275-5 |
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