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| DC 欄位 | 值 | 語言 |
|---|---|---|
| dc.contributor.advisor | 簡國龍(Kuo-Liong Chien) | |
| dc.contributor.author | Pei-Ying Wu | en |
| dc.contributor.author | 巫沛瑩 | zh_TW |
| dc.date.accessioned | 2021-05-20T19:58:42Z | - |
| dc.date.available | 2015-09-09 | |
| dc.date.available | 2021-05-20T19:58:42Z | - |
| dc.date.copyright | 2010-09-09 | |
| dc.date.issued | 2010 | |
| dc.date.submitted | 2010-07-11 | |
| dc.identifier.citation | 1. UNAIDS/WHO. 09 AIDS epidemic update 2009.
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| dc.identifier.uri | http://tdr.lib.ntu.edu.tw/jspui/handle/123456789/8590 | - |
| dc.description.abstract | 摘要
背景與目標:高效能抗反轉錄病毒療法可能會增加愛滋病毒感染者發生代謝症候群的風險,代謝症侯群的發生對於長期服用抗反轉錄病毒療法的感染者的健康來說是一大威脅。本研究的目的為調查台灣愛滋病毒感染者服用高效能抗反轉錄病毒療法後出現代謝症候群之盛行率及相關因子。 方法:我們採用橫斷性調查法,調查時間為 2008年5月至2009年5月,針對在臺灣大學附設醫院接受治療的愛滋病毒感染者,收集其基本人口學資料,身高、體重、腰圍、血壓,以及臨床檢驗結果;我們使用病歷回顧的方式,調查感染者服用高效能抗反轉錄病毒療法之狀況。我們採用2005年AHA/NHLBI-ATPⅢ所修訂的診斷標準做為診斷代謝症候群的標準,腰圍則是採用亞洲人的標準。 結果:我們一共收集877位個案,個案平均年齡為38.7歲,其中75.3%是男同性戀者,80.7%個案接受高效能抗反轉錄病毒療法,而88.7%個案的T細胞免疫球數≧200 cells/µl。我們發現210位有代謝症候群,代謝症候群盛行率為26.2%。在羅吉斯迴歸分析中,我們調整了年齡、性別、抽菸狀況、家族病史、以及愛滋病毒感染者被診斷時初次的T細胞免疫球數和愛滋病毒量之後,我們發現服用蛋白酶抑制劑者與代謝症候群之間仍然有很強的相關性 ,勝算比(odds ratio [OR], 1.63; 95% confidence interval [CI], 1.10-2.43)。此外,服用高效能抗反轉錄病毒療法超過六年以上、蛋白酶抑制劑三年以上者,以及核苷酸反轉錄酶抑制劑者大於六年以上者,與未服用藥物者比較,在調整潛在的干擾因子後,有代謝症候群的勝算比分別是1.96 (95% CI, 1.13-3.42),1.78 (95% CI, 1.03-3.07),及1.91 (95% CI, 1.11-3.30)。 結論:台灣愛滋病毒感染者服用高效能抗反轉錄病毒療法以及長期服用蛋白酶抑制劑、核苷酸反轉錄酶抑制劑與代謝症候群具有高度正相關。 | zh_TW |
| dc.description.abstract | Abstract
Background: Metabolic complications related to antiretroviral therapy are increasingly recognized as challenges to long-term management of HIV infection. We investigated the prevalence of and factors associated with metabolic syndrome among HIV-infected patients who are ethnic Chinese in the era of highly active antiretroviral therapy. Methods: A cross-sectional survey was performed to collect information of demographic and clinical characteristics and antiretroviral therapy prescribed among 877 patients with a mean age of 38.7 years who sought HIV care and received highly active antiretroviral therapy at a designated hospital for HIV care in Taiwan. The modified Adult Treatment Panel III criteria were used to define metabolic syndrome after adjusting for Asians in waist circumference. Results: Of the 877 patients, 75.3% were male homosexuals, 80.7% were receiving antiretroviral therapy, and 88.7% had CD4 counts ≧200 cells/µl when the survey was conducted. A total of 210 patients (26.2%) fulfilled the criteria for metabolic syndrome. In multiple logistic regression analysis after adjustment for age, gender, smoking status, family history of diabetes, cardiovascular disease and hypertension, and baseline CD4 and plasma HIV RNA load, use of protease inhibitors was the strongest associated factor with metabolic syndrome (odds ratio [OR], 1.63; 95% confidence interval [CI], 1.10-2.43). In addition, exposure to protease inhibitors for 3 years or greater, to highly active antiretroviral therapy for 6 years or greater, and to nucleoside reverse-transcriptase inhibitor(s) for 6 years or greater was statistically significantly associated with development of metabolic syndrome with an adjusted OR of 1.96 (95% CI, 1.13-3.42), 1.78 (95% CI, 1.03-3.07), and 1.91 (95% CI, 1.11-3.30), respectively. Conclusions: This is the first study to demonstrate the high prevalence of metabolic syndrome among HIV-infected patients who are ethnic Chinese. Receipt of HAART and prolonged exposure to protease inhibitors and nucleoside reverse transcriptase inhibitor(s) were associated with increased prevalence for metabolic syndrome. | en |
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| dc.description.tableofcontents | 摘要 I
Abstract II 致謝 III 目錄 IV List of tables VI List of figures IX 第一章 研究背景 1 第一節 愛滋病流行病學 1 1.1.1 全球及台灣感染人數 1 1.1.2 台灣愛滋病毒感染者罹患慢性病之情況 2 第二節 高效能抗反轉錄病毒療法使用情形 2 1.2.1 高效能抗反轉錄病毒療法的演進 2 1.2.2 台灣高效能抗反轉錄病毒療法之簡介 3 第三節 高效能抗反轉錄病毒療法之文獻查證 4 1.3.1 愛滋病病毒複製過程與三類抗反轉錄病毒藥物之作用機轉 4 1.3.2 三大類抗反轉錄病毒藥物之作用機轉 5 1.3.3 高效能抗反轉錄病毒療法之副作用 6 第四節 高效能抗反轉錄病毒療法與代謝症候群相關之文獻查證 7 1.4.1 蛋白酶抑制劑類藥物造成血脂異常之機轉 7 1.4.2 核苷酸反轉錄酶抑制劑藥物造成血脂異常之機轉 8 1.4.3 血脂異常 (Dyslipidemia) 9 1.4.4 胰島素阻抗 (Insulin resistance) 10 1.4.5 脂肪失養症 (Lipodystrophy) 10 1.4.6 糖尿病 (Diabetes mellitus) 11 1.4.7 高血壓 (Hypertension) 12 1.4.8 冠狀動脈心臟病 (Coronary heart disease) 13 1.4.9 代謝症候群 (Metabolic syndrome) 15 第五節 與過去研究的差異(Gap) 18 第二章目標/假說 20 研究假說 20 主要研究目的 20 次要研究目的 20 第三章 材料/方法 21 第一節 研究對象之資料收集 21 第二節 問卷及測量值之收集 21 第三節 研究對象之病歷回顧 22 第四節 診斷代謝症候群的標準 22 第五節 資料分析方法 22 3.5.1 高效能抗反轉錄病毒療法之定義 22 3.5.2 高效能抗反轉錄病毒療法服用時間之切點 23 3.5.3 樣本計算 (Sample size)及檢定力 (Power)之計算 23 3.5.4 資料變項準備及整理 24 3.5.5 描述性資料分析 24 3.5.6 推論統計 25 3.5.6 趨勢檢定 (Test for trend) 25 第四章 結果 26 第一節 研究對象基本資料 26 第二節 代謝症候群與基本資料之相關性 26 第三節 高效能抗反轉錄病毒療法與代謝症候群之相關性 27 4.3.1 整體服用高效能抗反轉錄病毒藥物之狀況 27 4.3.2 高效能抗反轉錄病毒療法服用時間長短與代謝症候群之相關性 28 第四節 蛋白酶抑制劑類藥物與代謝症候群之相關性 29 4.4.1 蛋白酶抑制劑類藥物服用的時間長短與代謝症候群之相關性 30 第五節 核苷酸反轉錄酶抑制類藥物與代謝症候群之相關性 31 4.5.1 核苷酸反轉錄酶抑制劑類藥物服用時間長短與代謝症候群之相關性………………….. 31 第六節 非核苷酸反轉錄酶抑制劑類藥物與代謝症候群之相關性 32 4.6.1 非核苷酸反轉錄酶抑制劑類藥物服用時間長短與代謝症候群之相關性…………. 32 第五章 討論 34 第一節 高效能抗反轉錄病毒療法與代謝症候群之相關 34 5.1.1 代謝症候群盛性率之比較 34 5.1.2 高效能抗反轉錄抗病毒療法與代謝症候群之相關性 36 5.1.3 高效能抗反轉錄病毒療法的服用時間長短與代謝症候群之相關性 ……………………………………………………………………………..37 5.1.4 高效能抗反轉錄病毒療法的服用時間長短與血脂、血壓、血糖之相關性………….. 37 第二節 蛋白酶抑制劑類藥物與代謝症候群之相關性 39 5.2.1 蛋白酶抑制劑類藥物與血脂、血壓、空腹血糖之相關性 40 5.2.2 蛋白酶抑制劑類藥物服用時間長短與代謝症候群之相關性 40 第三節 核苷酸反轉錄酶抑制劑類藥物與代謝症候群之相關性 41 5.3.1 核苷酸反轉錄酶抑制劑類藥物服用時間長短與代謝症候群之相 關性…………… 42 第四節 非核苷酸反轉錄酶抑制劑類藥物與代謝症候群之相關性 42 5.4.1 非核苷酸反轉錄酶抑制劑類藥物服用長短與代謝症候群之相關 42 第五節 個別藥物與代謝症候群之間相關性 43 第六節 結論 44 第七節 研究限制 45 參考文獻 46 List of tables TableⅠ-1: Literature review of the association between HAART and metabolic syndrome among HIV-infected patients 53 TableⅠ-1: Literature review of the association between HAART and metabolic syndrome among HIV-infected patients 54 TableⅠ-1: Literature review of the association between HAART and metabolic syndrome among HIV-infected patients 55 TableⅠ-2: Literature review of the association between HAART and hyperlipaemia among HIV-infected patients 56 TableⅠ-2: Literature review of the association between HAART and hyperlipaemia among HIV-infected patients 57 TableⅠ-3: Literature review of the association between HAART and diabetes mellitus among HIV-infected patients 58 TableⅠ-3: Literature review of the association between HAART and diabetes mellitus among HIV-infected patients 59 TableⅠ-4: Literature review about the association between HAART and CVD among HIV patients 60 TableⅠ-4: Literature review about the association between HAART and CVD among HIV patients 61 Table Ⅱ-1. Classes of antiretroviral agents 62 Table Ⅱ-2. Guideline for the use of hightly antiretroviral therapy in treatment-naïve patients 63 Table Ⅱ-3. Recommendations for initiation of combination antiretroviral therapy in adult patients 64 Table Ⅱ-4. Camparison of different diagnostic criteria for metabolic syndrome 65 Table Ⅲ-1. Characteristics of the 877 HIV-infected patients 66 Table Ⅲ-2. Camparison of clinical characteristics between HIV-infected patients with metabolic syndrome with those without metabolic syndrome 67 Table Ⅲ-3. The frequency of antiretroviral therapy in use 68 Table Ⅲ-4. Camparison of clinical characteristics between HIV-infected patients with metabolic syndrome with those without metabolic syndrome 69 Table Ⅲ-5. Odds ratio and 95% CI of the metabolic syndrome and different drug from multivariate analysis for selected variables 70 Table Ⅲ-6. Odds ratio and 95% CI for the association between different classes of drugs and the metabolic syndrome from multivariate analysis for selected variables 71 Table Ⅳ-1. Characteristics of 877 HIV-infected study population by duration of HAART 72 Table Ⅳ-1. Characteristics of 877 HIV-infected study population by duration of HAART (continued from previous page) 73 Table Ⅳ-2. Odds ratio and 95% CI for the association between metabolic syndrome and HAART duration in logistic regression 74 Table Ⅴ-1. Baseline characteristics of 877 patients by exposure to protease inhibitor 75 Table Ⅴ-2. Odds ratio and 95% CI for the association between exposure to protease inhibitor and the metabolic syndrome from multivariate analysis for selected variables 76 Table Ⅴ-3. Characteristics of 877 HIV-infected patients by duration of protease inhibitor 77 Table Ⅴ-3. Characteristics of 877 HIV-infected patients by duration of protease inhibitor (continued from previous page) 78 Table Ⅴ-4. Odds ratio and 95% CI for the association between metabolic syndrome and protease inhibitor duration in logistic regression 79 Table Ⅵ-1. Baseline characteristics of 877 patients by exposure to nucleos(t)ide reverse transcriptase 80 Table Ⅵ-2. Odds ratio and 95% CI for the association between exposure to nucleos(t)ide reverse transcriptase and the metabolic syndrome from multivariate analysis for selected variables 81 Table Ⅵ-3. Characteristics of 877 HIV-infected patients by duration of nucleos(t)ide reverse transcriptase 82 Table Ⅵ-3. Characteristics of 877 HIV-infected patients by duration of nucleos(t)ide reverse transcriptase (continued from previous page) 83 Table Ⅵ-4. Odds ratio and 95% CI for the association between metabolic syndrome and nucleos(t)ide reverse transcriptase duration in logistic regression 84 Table Ⅶ-1. Baseline characteristics of 877 patients by exposure to non-nucleoside reverse-transcriptase 85 Table Ⅶ-2. Odds ratio and 95% CI for the association between exposure to non-nucleoside reverse-transcriptase and the metabolic syndrome from multivariate analysis for selected variables 86 Table Ⅶ-3. Characteristics of 877 HIV-infected patients by duration of non-nucleoside reverse-transcriptase 87 Table Ⅶ-3. Characteristics of 877 HIV-infected patients by duration of non-nucleoside reverse-transcriptase (continued from previous page) 88 Table Ⅶ-4. Odds ratio and 95% CI for the association between metabolic syndrome and non-nucleoside reverse-transcriptase duration in logistic regression 89 Table Ⅷ-1. According to the changes mean ratios of HDL: total cholesterol at different antiretroviral therapy duration 90 Table Ⅷ-2. According to the changes mean ratios of total cholesterol : HDL at different antiretroviral therapy duration 91 Table Ⅸ-1. Univariate analyses of individual antiretroviral drugs and the metabolic syndrome 92 Table Ⅸ-2. Odds ratio and 95% CI for the association between metabolic syndrome and individual antiretroviral drugs in logistic regression 93 List of figures FigureⅠ-1. The time line approval of antiretroviral agaits 94 FigureⅠ-2. Life cycle of HIV with sites of action of antiretroviral agaits 95 FigureⅠ-3. The mechanism of HIV protease-inhibitor-induced hyperlipidaemia 96 FigureⅠ-4. The mechanism of fat metabolism in the hepatocytes 97 FigureⅠ-5. The mechanism of NRTI causing mitochondral toxicity and hyperlipidaemia 98 FigureⅡ-1. Study design and data collection 99 FigureⅡ-2. Flow chart of the study 100 FigureⅡ-3. Sample size and power plot 101 Figure Ⅲ-1. Mean serum triglyceride levels in 877 observed HIV-infected patients receiving HAART 102 Figure Ⅲ-2. Mean serum total cholesterol levels in 877 observed HIV-infected patients receiving HAART 103 Figure Ⅲ-3. Mean systolic blood pressure in 877 observed HIV-infected patients receiving HAART 104 Figure Ⅲ-4. Mean diastolic blood pressure in 877 observed HIV-infected patients receiving HAART 105 Figure Ⅲ-5. Mean serum fasting glucose levels in 877 observed HIV-infected patients receiving HAART 106 Figure Ⅲ-6.Mean serum triglyceride, total cholesterol, HDL, LDL, glucose in 877 HIV-infected patients during receiving HAART 107 Figure Ⅲ-7. Proportion with metabolic syndrome in 877 observed HIV-infected patients receiving HAART 108 Figure Ⅳ-1. Odds ratio and 95%CI for the association between HAART duration and metabolic syndrome 109 Figure Ⅴ-1. Odds ratio and 95%CI for the association between PI duration and metabolic syndrome 110 Figure Ⅵ-1. Odds ratio and 95%CI for the association between NRTI duration and metabolic syndrome 111 Figure Ⅶ-1. Odds ratio and 95%CI for the association between NNRTI duration and metabolic syndrome 112 Figure Ⅷ-1. According to the changes mean ratios of HDL: total cholesterol at different antiretroviral therapy duration 113 Figure Ⅷ-2. According to the changes mean ratios of total cholesterol : HDL at different antiretroviral therapy duration 114 | |
| dc.language.iso | zh-TW | |
| dc.title | 愛滋病毒感染者服用高效能抗反轉錄病毒療法後代謝症候群的盛行率及相關因素 | zh_TW |
| dc.title | Metabolic Syndrome among HIV-infected Taiwanese Patients in the Era of Highly Active Antiretroviral Therapy: Prevalence and Associated Factors | en |
| dc.type | Thesis | |
| dc.date.schoolyear | 98-2 | |
| dc.description.degree | 碩士 | |
| dc.contributor.coadvisor | 洪健清(Chien-Ching Hung) | |
| dc.contributor.oralexamcommittee | 楊偉勛(Wei-Shiung Yang),林錫勳(Sean-Shiung Lin),方啟泰(C-T Fang) | |
| dc.subject.keyword | 愛滋病毒感染,代謝症候群,高效能抗反轉錄病毒療法, | zh_TW |
| dc.subject.keyword | HIV infection,highly active antiretroviral therapy,metabolic syndrome, | en |
| dc.relation.page | 114 | |
| dc.rights.note | 同意授權(全球公開) | |
| dc.date.accepted | 2010-07-12 | |
| dc.contributor.author-college | 公共衛生學院 | zh_TW |
| dc.contributor.author-dept | 預防醫學研究所 | zh_TW |
| 顯示於系所單位: | 流行病學與預防醫學研究所 | |
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