β-Carotene in HIV infection : an extended evaluation
Several small short-term intervention studies have suggested that beta-carotene supplementation in HIV-infected patients can increase the number of various immune cells including CD4 cells. This prospective double-blinded study was designed to investigate whether beta-carotene supplementation would...
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Veröffentlicht in: | AIDS (London) 1996-08, Vol.10 (9), p.967-974 |
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description | Several small short-term intervention studies have suggested that beta-carotene supplementation in HIV-infected patients can increase the number of various immune cells including CD4 cells. This prospective double-blinded study was designed to investigate whether beta-carotene supplementation would result in this immuno-enhancement in a larger number of patients over a longer time period.
HIV-positive patients were randomly assigned to receive either 60 mg beta-carotene orally three times daily or a matched placebo. In addition, all patients received a multivitamin supplement. Patients were evaluated at baseline, 1 month, and 3 months for T-cell quantitative subsets, natural killer cells, HIV p24 antigen, beta-carotene levels, complete blood counts and chemistry batteries. Body weights and Karnofsky scores were evaluated at each visit.
Seventy-two patients signed informed consent forms and entered the study. Except for serum beta-carotene concentration, there were no statistically significant differences (P < 0.05) between the treatment (60 mg beta-carotene three times daily and multivitamins) and placebo (placebo and multivitamins) groups at baseline or after either 1 or 3 months of treatment.
Earlier studies suggesting that beta-carotene supplementation increased levels of immune cells in HIV-infected patients were not replicated in this study. The addition of a multivitamin supplement to both arms of this study may have masked any difference between the two groups. However, on the basis of the results of this study, we would not recommend supplementation with high doses of beta-carotene for HIV-infected patients. |
doi_str_mv | 10.1097/00002030-199610090-00006 |
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HIV-positive patients were randomly assigned to receive either 60 mg beta-carotene orally three times daily or a matched placebo. In addition, all patients received a multivitamin supplement. Patients were evaluated at baseline, 1 month, and 3 months for T-cell quantitative subsets, natural killer cells, HIV p24 antigen, beta-carotene levels, complete blood counts and chemistry batteries. Body weights and Karnofsky scores were evaluated at each visit.
Seventy-two patients signed informed consent forms and entered the study. Except for serum beta-carotene concentration, there were no statistically significant differences (P < 0.05) between the treatment (60 mg beta-carotene three times daily and multivitamins) and placebo (placebo and multivitamins) groups at baseline or after either 1 or 3 months of treatment.
Earlier studies suggesting that beta-carotene supplementation increased levels of immune cells in HIV-infected patients were not replicated in this study. The addition of a multivitamin supplement to both arms of this study may have masked any difference between the two groups. However, on the basis of the results of this study, we would not recommend supplementation with high doses of beta-carotene for HIV-infected patients.</description><identifier>ISSN: 0269-9370</identifier><identifier>EISSN: 1473-5571</identifier><identifier>DOI: 10.1097/00002030-199610090-00006</identifier><identifier>PMID: 8853729</identifier><language>eng</language><publisher>Hagerstown, MD: Lippincott Williams & Wilkins</publisher><subject>Administration, Oral ; AIDS/HIV ; beta Carotene - administration & dosage ; Biological and medical sciences ; Double-Blind Method ; HIV Core Protein p24 - analysis ; HIV Infections - blood ; HIV Infections - drug therapy ; HIV Infections - immunology ; HIV-1 - isolation & purification ; human immunodeficiency virus ; Humans ; Immunodeficiencies ; Immunodeficiencies. Immunoglobulinopathies ; Immunopathology ; Lymphocyte Count ; Medical sciences ; Prospective Studies ; T-Lymphocyte Subsets - immunology ; T-Lymphocyte Subsets - pathology ; T-Lymphocytes - immunology ; T-Lymphocytes - pathology ; Tropical medicine</subject><ispartof>AIDS (London), 1996-08, Vol.10 (9), p.967-974</ispartof><rights>1996 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c370t-5a93d1d6194b8c9b5ed927bfa9f29b7175fce8867be9f8c612a24a416d93a75d3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=3172488$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/8853729$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>COODLEY, G. O</creatorcontrib><creatorcontrib>COODLEY, M. K</creatorcontrib><creatorcontrib>LUSK, R</creatorcontrib><creatorcontrib>GREEN, T. R</creatorcontrib><creatorcontrib>BAKKE, A. C</creatorcontrib><creatorcontrib>WILSON, D</creatorcontrib><creatorcontrib>WACHENHEIM, D</creatorcontrib><creatorcontrib>SEXTON, G</creatorcontrib><creatorcontrib>SALVESON, C</creatorcontrib><title>β-Carotene in HIV infection : an extended evaluation</title><title>AIDS (London)</title><addtitle>AIDS</addtitle><description>Several small short-term intervention studies have suggested that beta-carotene supplementation in HIV-infected patients can increase the number of various immune cells including CD4 cells. This prospective double-blinded study was designed to investigate whether beta-carotene supplementation would result in this immuno-enhancement in a larger number of patients over a longer time period.
HIV-positive patients were randomly assigned to receive either 60 mg beta-carotene orally three times daily or a matched placebo. In addition, all patients received a multivitamin supplement. Patients were evaluated at baseline, 1 month, and 3 months for T-cell quantitative subsets, natural killer cells, HIV p24 antigen, beta-carotene levels, complete blood counts and chemistry batteries. Body weights and Karnofsky scores were evaluated at each visit.
Seventy-two patients signed informed consent forms and entered the study. Except for serum beta-carotene concentration, there were no statistically significant differences (P < 0.05) between the treatment (60 mg beta-carotene three times daily and multivitamins) and placebo (placebo and multivitamins) groups at baseline or after either 1 or 3 months of treatment.
Earlier studies suggesting that beta-carotene supplementation increased levels of immune cells in HIV-infected patients were not replicated in this study. The addition of a multivitamin supplement to both arms of this study may have masked any difference between the two groups. However, on the basis of the results of this study, we would not recommend supplementation with high doses of beta-carotene for HIV-infected patients.</description><subject>Administration, Oral</subject><subject>AIDS/HIV</subject><subject>beta Carotene - administration & dosage</subject><subject>Biological and medical sciences</subject><subject>Double-Blind Method</subject><subject>HIV Core Protein p24 - analysis</subject><subject>HIV Infections - blood</subject><subject>HIV Infections - drug therapy</subject><subject>HIV Infections - immunology</subject><subject>HIV-1 - isolation & purification</subject><subject>human immunodeficiency virus</subject><subject>Humans</subject><subject>Immunodeficiencies</subject><subject>Immunodeficiencies. Immunoglobulinopathies</subject><subject>Immunopathology</subject><subject>Lymphocyte Count</subject><subject>Medical sciences</subject><subject>Prospective Studies</subject><subject>T-Lymphocyte Subsets - immunology</subject><subject>T-Lymphocyte Subsets - pathology</subject><subject>T-Lymphocytes - immunology</subject><subject>T-Lymphocytes - pathology</subject><subject>Tropical medicine</subject><issn>0269-9370</issn><issn>1473-5571</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1996</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkE1OwzAQhS0EKqVwBKQsEDuDf-I_dqgCWqkSG2AbOfZYCkqTEjcIrsVBOBMODd0ym5HmfTNv9BDKKLmixKhrkooRTjA1RlJCDMHDSB6gKc0Vx0IoeoimhEmDDVfkGJ3E-JoIQbSeoInWgitmpkh8f-G57dotNJBVTbZYvqQWwG2rtsluMttk8JFEDz6Dd1v3dhBO0VGwdYSzsc_Q8_3d03yBV48Py_ntCrvkucXCGu6pl9TkpXamFOANU2WwJjBTKqpEcKC1VCWYoJ2kzLLc5lR6w60Sns_Q5e7upmvfeojbYl1FB3VtG2j7WCidE6q1_hekQnLJiEyg3oGua2PsIBSbrlrb7rOgpBiiLf6iLfbR_o6G1fPRoy_X4PeLY5ZJvxh1G52tQ2cbV8U9xqlieXr1B1QWf3c</recordid><startdate>19960801</startdate><enddate>19960801</enddate><creator>COODLEY, G. O</creator><creator>COODLEY, M. K</creator><creator>LUSK, R</creator><creator>GREEN, T. R</creator><creator>BAKKE, A. C</creator><creator>WILSON, D</creator><creator>WACHENHEIM, D</creator><creator>SEXTON, G</creator><creator>SALVESON, C</creator><general>Lippincott Williams & Wilkins</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7U9</scope><scope>H94</scope><scope>7X8</scope></search><sort><creationdate>19960801</creationdate><title>β-Carotene in HIV infection : an extended evaluation</title><author>COODLEY, G. O ; COODLEY, M. K ; LUSK, R ; GREEN, T. R ; BAKKE, A. C ; WILSON, D ; WACHENHEIM, D ; SEXTON, G ; SALVESON, C</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c370t-5a93d1d6194b8c9b5ed927bfa9f29b7175fce8867be9f8c612a24a416d93a75d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1996</creationdate><topic>Administration, Oral</topic><topic>AIDS/HIV</topic><topic>beta Carotene - administration & dosage</topic><topic>Biological and medical sciences</topic><topic>Double-Blind Method</topic><topic>HIV Core Protein p24 - analysis</topic><topic>HIV Infections - blood</topic><topic>HIV Infections - drug therapy</topic><topic>HIV Infections - immunology</topic><topic>HIV-1 - isolation & purification</topic><topic>human immunodeficiency virus</topic><topic>Humans</topic><topic>Immunodeficiencies</topic><topic>Immunodeficiencies. Immunoglobulinopathies</topic><topic>Immunopathology</topic><topic>Lymphocyte Count</topic><topic>Medical sciences</topic><topic>Prospective Studies</topic><topic>T-Lymphocyte Subsets - immunology</topic><topic>T-Lymphocyte Subsets - pathology</topic><topic>T-Lymphocytes - immunology</topic><topic>T-Lymphocytes - pathology</topic><topic>Tropical medicine</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>COODLEY, G. O</creatorcontrib><creatorcontrib>COODLEY, M. K</creatorcontrib><creatorcontrib>LUSK, R</creatorcontrib><creatorcontrib>GREEN, T. R</creatorcontrib><creatorcontrib>BAKKE, A. 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HIV-positive patients were randomly assigned to receive either 60 mg beta-carotene orally three times daily or a matched placebo. In addition, all patients received a multivitamin supplement. Patients were evaluated at baseline, 1 month, and 3 months for T-cell quantitative subsets, natural killer cells, HIV p24 antigen, beta-carotene levels, complete blood counts and chemistry batteries. Body weights and Karnofsky scores were evaluated at each visit.
Seventy-two patients signed informed consent forms and entered the study. Except for serum beta-carotene concentration, there were no statistically significant differences (P < 0.05) between the treatment (60 mg beta-carotene three times daily and multivitamins) and placebo (placebo and multivitamins) groups at baseline or after either 1 or 3 months of treatment.
Earlier studies suggesting that beta-carotene supplementation increased levels of immune cells in HIV-infected patients were not replicated in this study. The addition of a multivitamin supplement to both arms of this study may have masked any difference between the two groups. However, on the basis of the results of this study, we would not recommend supplementation with high doses of beta-carotene for HIV-infected patients.</abstract><cop>Hagerstown, MD</cop><pub>Lippincott Williams & Wilkins</pub><pmid>8853729</pmid><doi>10.1097/00002030-199610090-00006</doi><tpages>8</tpages></addata></record> |
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subjects | Administration, Oral AIDS/HIV beta Carotene - administration & dosage Biological and medical sciences Double-Blind Method HIV Core Protein p24 - analysis HIV Infections - blood HIV Infections - drug therapy HIV Infections - immunology HIV-1 - isolation & purification human immunodeficiency virus Humans Immunodeficiencies Immunodeficiencies. Immunoglobulinopathies Immunopathology Lymphocyte Count Medical sciences Prospective Studies T-Lymphocyte Subsets - immunology T-Lymphocyte Subsets - pathology T-Lymphocytes - immunology T-Lymphocytes - pathology Tropical medicine |
title | β-Carotene in HIV infection : an extended evaluation |
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