請用此 Handle URI 來引用此文件:
http://tdr.lib.ntu.edu.tw/jspui/handle/123456789/78680完整後設資料紀錄
| DC 欄位 | 值 | 語言 |
|---|---|---|
| dc.contributor.advisor | 于明暉(Ming-Whei Yu) | |
| dc.contributor.author | Mei-Ku Chen | en |
| dc.contributor.author | 陳美谷 | zh_TW |
| dc.date.accessioned | 2021-07-11T15:11:47Z | - |
| dc.date.available | 2024-06-30 | |
| dc.date.copyright | 2019-08-28 | |
| dc.date.issued | 2019 | |
| dc.date.submitted | 2019-08-05 | |
| dc.identifier.citation | [1] Puneet Puri and Arun J. Sanyal. Nonalcoholic fatty liver disease: Definitions, risk factors, and workup. Clinical Liver Disease. 2012;1:99-103.
[2] Anstee Quentin M, McPherson Stuart, Day Christopher P. How big a problem is non-alcoholic fatty liver disease? BMJ. 2011;343:d3897. [3] Younossi ZM, Koenig AB, Abdelatif D, et al. Global epidemiology of nonalcoholic fatty liver disease-Meta-analytic assessment of prevalence, incidence, and outcomes. Hepatology. 2016;64(1):73-84. [4] Younossi Z, Anstee QM, Marietti M, et al. Global burden of NAFLD and NASH: trends, predictions, risk factors and prevention. Nat Rev Gastroenterol Hepatol. 2018;15(1):11-20. [5] Ren-Nan Feng, Shan-Shan Du, Cheng Wang, et al. Lean-non-alcoholic fatty liver disease increases risk for metabolic disorders in a normal weight Chinese population. World J Gastroenterol. 2014;20(47):17932-17940. [6] Lallukka S, Sevastianova K, Perttilä J, et al. Adipose tissue is inflamed in NAFLD due to obesity but not in NAFLD due to genetic variation in PNPLA3. Diabetologia. 2013;56(4):886-92. [7] Younossi ZM, Stepanova M, Negro F, et al. Nonalcoholic fatty liver disease in lean individuals in the United States. Medicine. 2012;91(6):319-27. [8] Chalasani N, Younossi Z, Lavine JE, et al. The diagnosis and management of nonalcoholic fatty liver disease: Practice guidance from the American Association for the Study of Liver Diseases. Hepatology. 2018;67(1):328-357. [9] Martin-Rodriguez JL, Gonzalez-Cantero J, Gonzalez-Cantero A, et al. Diagnostic accuracy of serum alanine aminotransferase as biomarker for nonalcoholic fatty liver disease and insulin resistance in healthy subjects, using 3T MR spectroscopy. Medicine. 2017;96(17):e6770. [10] Lee YH, Cho Y, Lee BW, et al. Nonalcoholic Fatty Liver Disease in Diabetes. Part I: Epidemiology and Diagnosis. Diabetes Metab J. 2019;43(1):31-45. [11] European Association for the Study of the Liver (EASL), European Association for the Study of Diabetes (EASD) and European Association for the Study of Obesity (EASO). EASL-EASD-EASO Clinical Practice Guidelines for the management of non-alcoholic fatty liver disease. J Hepatol. 2016;64(6):1388-402. [12] Yu Y, Cai J, She Z and Li H. Insights into the Epidemiology, Pathogenesis, and Therapeutics of Nonalcoholic Fatty Liver Diseases. Adv Sci (Weinh). 2019;6(4):1801585. [13] Mummadi RR, Kasturi KS, Chennareddygari S and Sood GK. Effect of bariatric surgery on nonalcoholic fatty liver disease: systematic review and meta-analysis. Clin Gastroenterol Hepatol. 2008;6(12):1396-402. [14] Lee JY, Kim KM, Lee SG, et al. Prevalence and risk factors of non-alcoholic fatty liver disease in potential living liver donors in Korea: a review of 589 consecutive liver biopsies in a single center. J Hepatol. 2007;47(2):239-44. [15] Bedogni G, Miglioli L, Masutti F, et al. Prevalence of and risk factors for nonalcoholic fatty liver disease: the Dionysos nutrition and liver study. Hepatology. 2005;42(1):44-52. [16] Hamaguchi M, Kojima T, Takeda N, et al. The metabolic syndrome as a predictor of nonalcoholic fatty liver disease. Ann Intern Med. 2005;143(10):722-8. [17] Stefan N, Kantartzis K and Häring HU. Causes and metabolic consequences of Fatty liver. Endocr Rev. 2008;29(7):939-60. [18] Farrell GC and Larter CZ. Nonalcoholic fatty liver disease: from steatosis to cirrhosis. Hepatology. 2006;43(2 Suppl 1):S99-S112. [19] Anstee QM, Targher G and Day CP. Progression of NAFLD to diabetes mellitus, cardiovascular disease or cirrhosis. Nat Rev Gastroenterol Hepatol. 2013; 10(6):330-44. [20] Margini C and Dufour JF. The story of HCC in NAFLD: from epidemiology, across pathogenesis, to prevention and treatment. Liver Int. 2016;36(3):317-24. [21] Younossi ZM, Stepanova M, Afendy M, et al. Changes in the prevalence of the most common causes of chronic liver diseases in the United States from 1988 to 2008. Clin Gastroenterol Hepatol. 2011;9(6):524-530. [22] Anstee QM, Targher G and Day CP. Progression of NAFLD to diabetes mellitus, cardiovascular disease or cirrhosis. Nat Rev Gastroenterol Hepatol. 2013;10(6):330-44. [23] Alexis St. George, Adrian Bauman, Amanda Johnston, et al. Independent Effects of Physical Activity in Patients with Nonalcoholic Fatty Liver Disease. Hepatology. 2009;50:68-76. [24] Shira Zelber-Sagi, Dorit Zitzan-Kaluski, Rebecca Goldsmith, et al. Long term nutritional intake and the risk for non-alcoholic fatty liver disease (NAFLD): A population based study. Journal of Hepatology. 2007;47:711-717. [25] Chen L, Magliano DJ and Zimmet PZ. The worldwide epidemiology of type 2 diabetes mellitus--present and future perspectives. Nat Rev Endocrinol. 2011;8(4):228-36. [26] Glovaci D, Fan W and Wong ND. Epidemiology of Diabetes Mellitus and Cardiovascular Disease. Curr Cardiol Rep. 2019;21(4):21. [27] Klöppel G, Löhr M, Habich K, Oberholzer M and Heitz PU. Islet pathology and the pathogenesis of type 1 and type 2 diabetes mellitus revisited. Surv Synth Pathol Res. 1985;4(2):110-25. [28] Levy BI1, Schiffrin EL, Mourad JJ, et al. Impaired tissue perfusion: a pathology common to hypertension, obesity, and diabetes mellitus. Circulation. 2008;118(9):968-76. [29] Inzucchi SE, Bergenstal RM, Buse JB, et al. Management of hyperglycemia in type 2 diabetes, 2015: a patient-centered approach: update to a position statement of the American Diabetes Association and the European Association for the Study of Diabetes. Diabetes Care. 2015;38(1):140-9. [30] Shibata M, Kihara Y, Taguchi M, et al. Nonalcoholic fatty liver disease is a risk factor for type 2 diabetes in middle-aged Japanese men. Diabetes Care. 2007;30(11):2940-4. [31] Park SK, Seo MH, Shin HC and Ryoo JH. Clinical availability of nonalcoholic fatty liver disease as an early predictor of type 2 diabetes mellitus in Korean men: 5-year prospective cohort study. Hepatology. 2013;57(4):1378-83. [32] Yamazaki H, Tsuboya T, Tsuji K, et al. Independent Association Between Improvement of Nonalcoholic Fatty Liver Disease and Reduced Incidence of Type 2 Diabetes. Diabetes Care. 2015;38(9):1673-9. [33] Sung KC, Jeong WS, Wild SH and Byrne CD. Combined influence of insulin resistance, overweight/obesity, and fatty liver as risk factors for type 2 diabetes. Diabetes Care. 2012;35(4):717-22. [34] Arase Y, Suzuki F, Ikeda K, et al. Multivariate analysis of risk factors for the development of type 2 diabetes in nonalcoholic fatty liver disease. J Gastroenterol. 2009;44(10):1064-70. [35] Cheng YL, Wang YJ, Kao WY, et al. Inverse Association between Hepatitis B Virus Infection and Fatty Liver Disease: A Large-Scale Study in Populations Seeking for Check-Up. PLoS One. 2013;8(8):e72049. [36] Jan CF, Chen CJ, Chiu YH, et al. A population-based study investigating the association between metabolic syndrome and hepatitis B/C infection (Keelung Community-based Integrated Screening study No. 10). Int J Obes (Lond). 2006;30(5):794-9. [37] Wang CC, Hsu CS, Liu CJ, et al. Association of chronic hepatitis B virus infection with insulin resistance and hepatic steatosis. J Gastroenterol Hepatol. 2008;23(5):779-82. [38] Wang MM, Wang GS, Shen F, et al. Hepatic steatosis is highly prevalent in hepatitis B patients and negatively associated with virological factors. Dig Dis Sci. 2014;59(10):2571-9. [39] Bondini S, Kallman J, Wheeler A, et al. Impact of non-alcoholic fatty liver disease on chronic hepatitis B. Liver Int. 2007;27(5):607-11. [40] Xiong J, Zhang H, Wang Y, et al. Hepatitis B virus infection and the risk of nonalcoholic fatty liver disease: a meta-analysis. Oncotarget. 2017;8(63):107295-107302. [41] Kim KH, Shin HJ, Kim K, et al. Hepatitis B Virus X Protein Induces Hepatic Steatosis Via Transcriptional Activation of SREBP1 and PPARγ. Gastroenterology. 2007;132(5):1955-67. [42] Kim JY, Song EH, Lee HJ, et al. HBx-induced hepatic steatosis and apoptosis are regulated by TNFR1- and NF-kappaB-dependent pathways. J Mol Biol. 2010;397(4):917-31. [43] Shieh YS, Chang YS, Hong JR, et al. Increase of hepatic fat accumulation by liver specific expression of Hepatitis B virus X protein in zebrafish. Biochim Biophys Acta. 2010;1801(7):721-30. [44] Wong VW, Wong GL, Chu WC, et al. Hepatitis B virus infection and fatty liver in the general population. J Hepatol. 2012;56(3):533-40. [45] Lonardo A, Adinolfi LE, Loria P, et al. Steatosis and hepatitis C virus: mechanisms and significance for hepatic and extrahepatic disease. Gastroenterology. 2004;126(2):586-97. [46] Kumar D, Farrell GC, Fung C and George J. Hepatitis C virus genotype 3 is cytopathic to hepatocytes: Reversal of hepatic steatosis after sustained therapeutic response. Hepatology. 2002;36(5):1266-72. [47] Hung YC, Lin CL, Liu CJ, et al. Development of risk scoring system for stratifying population for hepatocellular carcinoma screening. Hepatology. 2015;61(6):1934-44. [48] Nathalie C. Leite, Gil F. Salles, Antonio L. E. Araujo, et al. Prevalence and associated factors of non‐alcoholic fatty liver disease in patients with type‐2 diabetes mellitus. Liver International. 2009;29(1):113-9. [49] Chan WK, Tan AT, Vethakkan SR, et al. Non-alcoholic fatty liver disease in diabetics – prevalence and predictive factors in a multiracial hospital clinic population in Malaysia. J Gastroenterol Hepatol. 2013;28(8):1375-83. [50] Wong RJ, Liu B, Bhuket T, et al. Significant burden of nonalcoholic fatty liver disease with advanced fibrosis in the US: a cross-sectional analysis of 2011-2014 National Health and Nutrition Examination Survey. Aliment Pharmacol Ther. 2017;46(10):974-980. [51] Machado MV, Oliveira AG and Cortez-Pinto H. Hepatic steatosis in hepatitis B virus infected patients: Meta-analysis of risk factors and comparison with hepatitis C infected patients. J Gastroenterol Hepatol. 2011;26(9):1361-7. [52] Yilmaz B, Koklu S, Buyukbayram H et al. Chronic hepatitis B associated with hepatic steatosis, insulin resistance, necroinflammation and fibrosis. Afr Health Sci. 2015;15(3):714–718. [53] Adams LA, Waters OR, Knuiman MW, et al. NAFLD as a Risk Factor for the Development of Diabetes and the Metabolic Syndrome: An Eleven-Year Follow-up Study. Am J Gastroenterol. 2009;104(4):861-7. [54] Gordon A, McLean CA, Pedersen JS, et al. Hepatic steatosis chronic hepatitis B and C: Predictors, distribution and effect on fibrosis. J Hepatol. 2005;43(1):38-44. [55] Minakari M, Molaei M, Shalmani HM, et al. Liver steatosis in patients with chronic hepatitis B infection: host and viral risk factors. Eur J Gastroenterol Hepatol. 2009;21(5):512-6. [56] Peng D, Han Y, Ding H and Wei L. Hepatic steatosis in chronic hepatitis B patients is associated with metabolic factors more than viral factors. J Gastroenterol Hepatol. 2008;23(7Pt1):1082-8. [57] Yamada T, Fukatsu M, Suzuki S, et al. Fatty liver predicts impaired fasting glucose and type 2 diabetes mellitus in Japanese undergoing a health checkup. J Gastroenterol Hepatol.2010;25(2):352-6. [58] Chon CW, Kim BS, Cho YK, et al. Effect of Nonalcoholic Fatty Liver Disease on the Development of Type 2 Diabetes in Nonobese, Nondiabetic Korean Men. Gut Liver. 2012;6(3):368-73. [59] Fukuda T, Hamaguchi M, Kojima T, et al. The impact of non-alcoholic fatty liver disease on incident type 2 diabetes mellitus in non-overweight individuals. Liver Int. 2016;36(2):275-83. [60] Kim HJ, Lee KE, Kim DJ, et al. Metabolic Significance of Nonalcoholic Fatty Liver Disease in Nonobese, Nondiabetic Adults. Arch Intern Med. 2004;164(19):2169-75. [61] Das K, Das K, Mukherjee PS, et al. Nonobese Population in a Developing Country Has a High Prevalence of Nonalcoholic Fatty Liver and Significant Liver Disease. Hepatology. 2010;51(5):1593-602. [62] Kwon YM, Oh SW, Hwang SS, et al. Association of nonalcoholic fatty liver disease with components of metabolic syndrome according to body mass index in Korean adults. Am J Gastroenterol. 2012;107(12):1852-8. [63] Younossi ZM, Stepanova M, Negro F, et al. Nonalcoholic fatty liver disease in lean individuals in the United States. Medicine (Baltimore). 2012;91(6):319-27. [64] Feng RN, Du SS, Wang C, et al. Lean-non-alcoholic fatty liver disease increases risk for metabolic disorders in a normal weight Chinese population. World J Gastroenterol. 2014;20(47):17932–17940. [65] Honda Y, Yoneda M, Kessoku T, et al. Characteristics of non-obese non-alcoholic fatty liver disease: Effect of genetic and environmental factors. Hepatol Res. 2016;46(10):1011-8. [66] Leung JC, Loong TC, Wei JL, et al. Histological severity and clinical outcomes of nonalcoholic fatty liver disease in nonobese patients. Hepatology. 2017;65(1):54-64. [67] Feldman A, Eder SK, Felder TK, et al. Clinical and Metabolic Characterization of Lean Caucasian Subjects With Non-alcoholic Fatty Liver. Am J Gastroenterol. 2017;112(1):102-110. [68] Kotronen A, Yki-Järvinen H, Männistö S, et al. Non-alcoholic and alcoholic fatty liver disease - two diseases of affluence associated with the metabolic syndrome and type 2 diabetes: the FIN-D2D survey. BMC Public Health. 2010;10:237. | |
| dc.identifier.uri | http://tdr.lib.ntu.edu.tw/jspui/handle/123456789/78680 | - |
| dc.description.abstract | 背景及研究目的
一般族群中,脂肪肝與第二型糖尿病相關,但此關係在HBV患者是否成立仍不清楚。本研究使用縱貫性研究來探討HBV男性病患中,脂肪肝與新診斷第二型糖尿病的相關性,並進一步討論瘦型人與胖型人對此關係的影響。 材料與方法 本研究使用台灣公務人員保險聯合門診研究資料,從2005年追蹤至2018年,研究對象為1208位HBsAg陽性且在第一次來檢時無第二型糖尿病的男性(包含66位HBV/HCV共同感染的患者),並於追蹤期間重複回診做全面檢查(包含肝臟超音波、血液檢查及人體學檢查)。脂肪肝使用腹部超音波診斷,而糖尿病定義為空腹血糖值≥126 mg/dL或有第二型糖尿病史。共有332位研究對象在十年中有四次或四次以上的健檢回診資料。使用多變項羅吉斯迴歸來研究脂肪肝情形和發生糖尿病的相對危險比(OR),以及縱貫性研究使用重複事件Cox比例風險模型。 結果 第一次來檢時,脂肪肝的盛行率為39.2%。平均追蹤8.7±3.1年後,121位研究對象(10.0%)新診斷出第二型糖尿病。多變項迴歸分析顯示脂肪肝相較於無脂肪肝者,其危險性為1.97倍(95%CI=1.25-3.11),此關係獨立於空腹血糖異常(IFG)、BMI及血脂。對於332位在十年中有四次或四次以上的健檢回診資料的研究對象,脂肪肝造成新診斷第二型糖尿病的風險比為2.80(95%CI=1.23-6.40)。相對於胖型人,此關係在瘦型人中更加明顯。在瘦型人當中,脂肪肝相對於無脂肪肝造成新診斷第二型糖尿病的危險性達9倍之多。不考慮BMI的話,IFG是脂肪肝造成新診斷第二型糖尿病的最重要的危險因子。 iv 結論 在男性HBV帶原者中,脂肪肝會增加罹患第二型糖尿病的危險性且獨立於代謝危險因子,而且相對於胖型人,瘦型人的脂肪肝效應更加顯著。 | zh_TW |
| dc.description.abstract | Background and Aim
Fatty liver has been associated with type 2 diabetes (T2DM) in general population, but its role among people infected with hepatitis B virus (HBV) is unclear. We used a longitudinal study to investigate the association between fatty liver and the development of T2DM in men with HBV, and to understand the impact of lean or obese body mass on this relationship. Material and Methods Clinical and laboratory data from Taiwan’s Government Employees’ Central Clinic were assessed in 1,208 (including 66 with HBV/HCV dual infection) HBsAg positive men who were free of T2DM at initial examination and were examined repeatedly with a comprehensive investigation (including liver ultrasonography, blood testing, and anthropometric measurements) between 2005 and 2018. Fatty liver was diagnosed by abdominal ultrasound, and diabetes was defined as fasting blood glucose≥126 mg/dL or having a history of T2DM. A total of 332 participants had four or more check-up records in ten years. We used multivariate logistic regression to investigate fatty liver status and OR of development T2DM, and repeated events Cox’s proportional hazards model in longitudinal study. vi Results At initial examination, the prevalence of fatty liver was 39.2%. After an average of 8.7±3.1 years of follow-up, 121 study subjects (10.0%) developed T2DM. Multivariate analysis showed that the risk of T2DM was 1.97 (95% CI=1.25-3.11) times higher among subjects with fatty liver than those without. This association was independent of impaired fasting glucose, body mass index (BMI), and blood lipids. For the 332 subjects who had ≥ 4 clinical visits in 10 years, the hazard ratio of T2DM associated with fatty liver was 2.80 (95% CI=1.23-6.40). This association was more striking among subjects with lean body mass than those with obese body mass. Among those with lean body mass, fatty liver was associated with a 9-fold higher risk of developing T2DM. Impaired fasting glucose was the most important risk factor for T2DM among patients with fatty liver, irrespective of body mass. Conclusions In male HBV carriers, fatty liver increased risk of T2DM independent of other metabolic risk factors, and the effect of fatty liver was more striking among subjects with lean body mass than those with obese body mass. | en |
| dc.description.provenance | Made available in DSpace on 2021-07-11T15:11:47Z (GMT). No. of bitstreams: 1 ntu-108-R06849024-1.pdf: 4425384 bytes, checksum: 89b63baa7df068386e91d2fc055d026d (MD5) Previous issue date: 2019 | en |
| dc.description.tableofcontents | 目錄
口試委員會審定書 i 誌謝 ii 中文摘要 iii 英文摘要 v 圖表目錄 viii 第一章 研究背景 1 第一節 非酒精性脂肪肝病(NAFLD) 1 第二節 糖尿病 3 第三節 脂肪肝與糖尿病的關聯 4 第四節 B型肝炎與脂肪肝 6 第五節 C型肝炎與脂肪肝 6 第六節 研究目的 7 第二章 材料和方法 8 第一節 研究世代 8 第二節 變項定義 8 第三節 統計分析 9 第三章 結果 11 第一節 各變項與脂肪肝的相關性(2005-2018年) 11 第二節 脂肪肝和代謝危險因子的迴歸分析 11 第三節 脂肪肝在不同身型與糖尿病危險性的相關性 12 第四章 討論 15 第一節 脂肪肝與血糖的相關性 15 第二節 脂肪肝與糖尿病危險性的因果關係 15 第三節 不同身型(瘦型、胖型)的脂肪肝與代謝症候群的關係 17 第四節 不同身型(瘦型、胖型)的脂肪肝與糖尿病的關係 18 第五節 限制與建議 20 第六節 結論 21 參考文獻 22 圖表目錄 表一. 2005-2018年追蹤期間依有無脂肪肝分組的第一次來檢與最後一次來檢之特性分布 30 表二. 第一次來檢1208位血糖正常者,其脂肪肝和各代謝因子特性與追蹤發生糖尿病的相對危險比 33 表三. 第一次來檢血糖正常且十年內有四次來檢資料的332位個案,隨時間變化的各變項特性與追蹤期間發生糖尿病的變化的風險比 34 表四. 比較十年來檢四次者與扣除前者受試者的基線基礎特性分析 35 表五-1. 第一次來檢依身型分組(瘦型、胖型),其基線脂肪肝情形與追蹤發生糖尿病的相對危險比 37 表五-2. 第一次來檢依身型分組(瘦型、不胖型、胖型),其基線脂肪肝情形與追蹤發生糖尿病的相對危險比 38 表六-1. 第一次來檢代謝因子組成在有無脂肪肝狀態的分布情形:以身型瘦胖分組(BMI<25、BMI≥25) 39 表六-2. 最後一次來檢代謝因子組成在有無脂肪肝狀態的分布情形:以身型瘦胖分組(BMI<25、BMI≥25 41 表六-3. 第一次來檢代謝因子組成在有無脂肪肝狀態的分布情形:以身型瘦胖分組(BMI<23、23≤BMI<25、BMI≥25) 43 表六-4. 最後一次來檢代謝因子組成在有無脂肪肝狀態的分布情形:以身型瘦胖分組(BMI<23、23≤BMI<25、BMI≥25) 45 表七-1. 第一次及最後一次來檢代謝因子組成在不同身型(胖型、瘦型)脂肪肝患者的分布情形 47 表七-2. 第一次及最後一次來檢代謝因子組成在不同身型(瘦型、不胖型、胖型)脂肪肝患者的分布情形 49 表八-1. 第一次來檢控制不同代謝因子情形下瘦型(BMI<25)脂肪肝患者的追蹤發生糖尿病相對危險比 51 表八-2. 第一次來檢控制不同代謝因子情形下胖型(BMI≥25)脂肪肝患者的追蹤發生糖尿病相對危險比 52 | |
| dc.language.iso | zh-TW | |
| dc.subject | 非酒精性脂肪肝病、第二型糖尿病、B型肝炎帶原者、肥胖、IFG | zh_TW |
| dc.subject | hepatitis B virus carrier | en |
| dc.subject | obesity | en |
| dc.subject | impaired fasting glucose | en |
| dc.subject | type 2 diabetes | en |
| dc.subject | non-alcoholic fatty liver disease | en |
| dc.title | B型肝炎帶原者非酒精性脂肪肝病與第二型糖尿病危險性之縱貫性研究 | zh_TW |
| dc.title | Non-alcoholic Fatty liver Disease and Risk of Type II Diabetes Mellitus in Hepatitis B Virus Carriers: Longitudinal Study | en |
| dc.type | Thesis | |
| dc.date.schoolyear | 107-2 | |
| dc.description.degree | 碩士 | |
| dc.contributor.oralexamcommittee | 廖勇柏,李文宗,林志陵,黃奕文 | |
| dc.subject.keyword | 非酒精性脂肪肝病、第二型糖尿病、B型肝炎帶原者、肥胖、IFG, | zh_TW |
| dc.subject.keyword | non-alcoholic fatty liver disease, type 2 diabetes, hepatitis B virus carrier, obesity, impaired fasting glucose, | en |
| dc.relation.page | 52 | |
| dc.identifier.doi | 10.6342/NTU201902581 | |
| dc.rights.note | 有償授權 | |
| dc.date.accepted | 2019-08-06 | |
| dc.contributor.author-college | 公共衛生學院 | zh_TW |
| dc.contributor.author-dept | 流行病學與預防醫學研究所 | zh_TW |
| dc.date.embargo-lift | 2024-06-30 | - |
| 顯示於系所單位: | 流行病學與預防醫學研究所 | |
文件中的檔案:
| 檔案 | 大小 | 格式 | |
|---|---|---|---|
| ntu-108-R06849024-1.pdf 未授權公開取用 | 4.32 MB | Adobe PDF |
系統中的文件,除了特別指名其著作權條款之外,均受到著作權保護,並且保留所有的權利。
