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  1. NTU Theses and Dissertations Repository
  2. 公共衛生學院
  3. 流行病學與預防醫學研究所
請用此 Handle URI 來引用此文件: http://tdr.lib.ntu.edu.tw/jspui/handle/123456789/57824
完整後設資料紀錄
DC 欄位值語言
dc.contributor.advisor杜裕康(Yu-Kang Tu)
dc.contributor.authorTsung-Ying Hsiehen
dc.contributor.author謝宗穎zh_TW
dc.date.accessioned2021-06-16T07:05:48Z-
dc.date.available2016-10-20
dc.date.copyright2014-10-20
dc.date.issued2014
dc.date.submitted2014-07-10
dc.identifier.citation[1] Greenland S., Longnecker M. P.. Methods for Trend Estimation from Summarized Dose-Response Data, with Applications to Meta-Analysis. American Journal of Epidemiology 1992; 135: 1301-1309.
[2] Liu Q., Cook N. R., Bergstorm A., Hsieh C. C.. A two-stage hierarchical regression model for meta-analysis of epidemiologic nonlinear dose-response data. Computational Statistics and Data Analysis 2009; 28:1218-1237.
[3] Orsini N., Bellocco R., Greenland S.. Generalized lease squares for trend estimation of summarized dose-response data. Stata Journal 2006; 6: 40-57.
[4] Orsini N, Li R., Wolk A., Khudyakov P., Spiegelman D.. Meta-analysis for linear and nonlinear dose-response relations: examples, an evaluation of approximations, and software. American Journal of Epidemiology 2011; 175: 66-73.
[5] Rota M., Bellocco R., Scotti L., Tramacere I., Jenab M., Corrao G., La Vecchia C., Boffetta P., Bagnardi V.. Random-effects meta-regression models for studying nonlinear dose–response relationship, with an application to alcohol and esophageal squamous cell carcinoma. Statistics in Medicine 2010; 29:2679–2687.
[6] Taylor G. W., Burt B. A., Becker M. P., Genco R. J., Shlossman M., Knowler W. C., Pettiti D. J.. Severe Periodontitis and Risk for Poor Glycemie Control in Patients with Non- Insulin-Dependent Diabetes Mellitus. Journal of Periodontal 1996; 67:1085-1093.
[7] Tomita N. E., Chinellato L. E., Pernambuco R. A., Lauris J. R., Franco L. J.. Periodontal conditions and diabetes mellitus in the Japanese-Brazilian population. Revista de Saude Publica 2002; 36(5):607-613.
[8]-[9] Tsai C., Hayes C., Taylor G. W.. Glycemic control of type 2 diabetes and severe periodontal disease in the US adult population. Community Dentistry and Oral Epidemiology 2002; 30:182-192.
[10] Saito T., Shimazaki Y., Kiyohara Y., Kato I., Kubo M., Iida M., Koga T.. The Severity of Periodontal Disease is Associated with the Development of Glucose Intolerance in Non-diabetics: The Hisayama Study. Journal of Dental Research 2004; 83(6):485-490.
[11] Diaz-Romero R. M., Casanova-Roman G., Beltran-Zuniga M., Belmont-Padilla J., Mendez J. D., Avila-Rosas H.. Oral Infections and Glycemic Control in Pregnant Type 2 Diabetics. Archives of Medical Research 2005; 36:42-48.
[12] Campus G., Salem A., Uzzau S., Baldoni E., Tonolo G.. Diabetes and Periodontal Disease: A Case-Control Study. Journal of Periodontal 2005;76:418-425.
[13] Saito T., Murakami M., Shimazaki Y., Matsumoto S., Yamashita Y.. The Extent of Alveolar Bone Loss Is Associated With Impaired Glucose Tolerance in Japanese Men. Journal of Periodontal 2006; 77:392-397.
[14] Leung W. K. , Movva L. R., Wong M. C., Corbet E. F., Siu S. C., Kawamura M.. Health behavior, metabolic control and periodontal status in medically treated Chinese with type 2 diabetes mellitus. Annals of the Royal Australasian College of Dental Surgeons 2008; 19:102-110.
[15] Gonzalez-Guevara M. B., Linares-Vieyra C., Luis Enrique Rodriguez-de Mendoza L. E.. Prevalence of buccal lesions on type 2 diabetes mellitus. Revista Medica del Instituto Mexicano del Seguro Social 2008; 46(3):237-245.
[16] Leung, W. K., Siu S. C., Chu F. C., Wong K. W., Jin L., Sham A. S., Tsang C. S., Samaranayake L. P.. Oral Health Status of Low-income, Middle-aged to Elderly Hong Kong Chinese with Type 2 Diabetes Mellitus. Oral Health and Preventive Dentistry 2008; 6:105-118.
[17] Wang T. T., Chen T. H., Wang P. E., Lai H., Lo M. T., Chen P. Y., Chiu S. Y.. A population-based study on the association between type 2 diabetes and periodontal disease in 12,123 middle-aged Taiwanese (KCIS No. 21). Journal of Clinical Periodontology 2009; 36:372-379.
[18] Preshaw P. M., de Silva N., McCracken G. I., Fernando D. J., Dalton C. F., Steen N. D., Heasman P. A.. Compromised periodontal status in an urban Sri Lankan population with type 2 diabetes. Journal of Clinical Periodontology 2010; 37: 165–171.
[19] Zadik Y., Bechor R., Galor S., Levin L.. Periodontal disease might be associated even with impaired fasting glucose. British Dental Journal 2010; 208:E20.
[20] Gomes-Filho I. S., Freitas Coelho J. M., da Cruz S. S., Passos J. S., Teixeira de Freitas C. O., Aragao Farias N. S., Amorim da Silva R., Silva Pereira M. N., Lima T. L., Barreto M. L.. Chronic Periodontitis and C-Reactive Protein Levels. Journal of Periodontal 2011; 82:969-978.
[21] Das M., Upadhyaya V., Ramachandra S. S., Jithendra K. D.. Periodontal treatment needs in diabetic and non-diabetic individuals: A case-control study. Indian Journal of Dental Research 2011; 22:291-294.
[22] Awuti G., Younusi K., Li L., Upur H., Ren J.. Epidemiological Survey on the Prevalence of Periodontitis and DiabetesMellitus in Uyghur Adults fromRural Hotan Area in Xinjiang. Journal of Diabetes Research 2012; Volume 2012, Article ID 758921, 7 pages.
[23] Botero J. E., Yepes F. L., Roldan N., Castrillon C. A., Hincapie J. P., Ochoa S. P., Ospina C. A., Becerra M. A., Jaramillo A., Gutierrez S. J., Contreras A.. Tooth and Periodontal Clinical Attachment Loss Are Associated With Hyperglycemia in Patients With Diabetes. Journal of Periodontal 2012; 83:1245-1250.
[24] Hodge P. J., Robertson D., Paterson K., Smith G. L., Creanor S., Sherriff A.. Periodontitis in non-smoking type 1 diabetic adults: a cross-sectional study. Journal of Clinical Periodontology 2012; 39: 20–29.
[25]-[26] Javed F., Tenenbaum H. C., Nogueira-Filho G., Nooh N., O’Bello Correa F., Warnakulasuriya S., Dasanayake A. P., Al-Hezaimi K.. Periodontal Inflammatory Conditions Among Gutka Chewers and Non-chewers With and Without Prediabetes. Journal of Periodontal 2013;84:1158-1164.
[27] Susanto H., Nesse W., Dijkstra P. U., Hoedemaker E., van Reenen Y. H., Agustina D., Vissink A., Abbas F... Periodontal inflamed surface area and C-reactive protein as predictors of HbA1c: a study in Indonesia. The journal Clinical Oral Investigations 2012; 16:1237–1242.
[28] Kim E. K., Lee S. G., Choi Y. H., Won K. C., Moon J. S., Merchant A. T., Lee H. K.. Association between diabetes-related factors and clinical periodontal parameters in type-2 diabetes mellitus. BMC Oral Health 2013; 13:64.
[29] Katz J.. Elevated blood glucose levels in patients with severe periodontal disease. Journal of Clinical Periodontology 2001; 28: 710-712.
dc.identifier.urihttp://tdr.lib.ntu.edu.tw/jspui/handle/123456789/57824-
dc.description.abstract背景
系統性文獻回顧以及統合分析在證據整合上應用的非常廣泛,研究者利用傳統統合分析對從系統性文獻回顧中找到的證據進行兩組之間的統合比較,但許多的觀察性研究會探討多個劑量類別與結果(效應)之間的關係。劑量與效應反應的統合分析(dose-response meta-analysis)中,每一劑量組均會與同一基準組進行比較,此時劑量類別與劑量類別的勝算比間具有相關性,現今常使用的統計軟體中需要每一劑量類別下的人數及事件發生人數來計算此相關性。如此,研究者則可藉由此方法了解藥物在何等劑量之下能達到最大的治療效益;或者疾病風險在何種暴露量下會達到最大的風險。
目的
本論文的研究目的主要發展一方法以補齊無提供每一劑量類別下之人數及事件發生人數的文獻其結果與結果間之相關係數,具體的目標如下:
1. 發展generalized least square (GLS)模型於固定效應的劑量與效應反應統合分析上,以算出無提供人數之文獻其結果與結果間之相關係數。
2. 發展R程式以應用GLS模型,基於每一劑量類別下之人數及事件發生人數已知以及未知的情況。
3. 發展R程式以應用GLS模型,以研究血糖值與牙周病風險之間的關聯。
資料來源
本論文實際進行系統性文獻回顧,收集血糖值與牙周病間的關係之文獻以及使用酒精與心血管疾病間的關係之資料以應用於本論文的統計方法。

結果
1. 本研究以GLS方法以及restricted cubic splines模型分析資料「血糖值與牙周病間的關係」:發現隨著血糖值的上升;牙周病的勝算亦是增加。
2. 本研究中發展R程式基於'pool-first'或是'pool-last'的統合架構下應用GLS,所統合得到的結果與Orsini等人利用Stata軟體以及Liu與Rota等人利用SAS軟體統合分析之結果相同。
3. 本研究假設暴露類別與暴露類別其勝算比間之相關係數為0.5來統合得到之結果,與透過實際人數所求得之相關係數而所統合的結果一致,此舉對於未來進行系統性文獻回顧時,能留下符合主題卻無報告每一劑量類別下的人數以及事件發生人數之文獻進入統合分析。
結論
Greenland與Longnecker所提出之GLS方法能有效的於統合估計時將劑量組與劑量組其勝算比間的相關性考慮進去,但需要每一劑量類別下之人數及事件發生人數來計算此相關性。而Orsini等人提出之restricted cubic splines模型提供研究者有效地於劑量與效應之間估計非線性的關係。此外,本研究所提出之相關係數的假設則供研究者能增加於統合分析時之文獻樣本。
zh_TW
dc.description.abstractBackground
Systematic reviews and meta-analysis are widely used for evidence synthesis. Traditional meta-analysis compare difference in outcomes between two interventions/treatments, but in observational studies, comparisons are sometimes made for groups with different levels of exposure to risk factors. Dose-response meta-analysis transforms the discrete levels of an exposure back to a continuous variable and then estimates a linear or nonlinear relation between the outcome (the response) and continuous exposure (the doses). However, as multiple levels of exposure are usually reported in a study, the outcomes are therefore not independent, and current statistical model for dose-response meta-analysis requires the input of the number of subjects with or without the outcome event at different levels of exposure to calculate the correlations between the outcomes.
Objectives
The main objective of this dissertation is to develop an alternative approach by imputing missing information for correlations between outcomes. The specific objectives are:
1. Developing generalized least squares (GLS) models for fixed effects dose-response analysis, when the correlations between outcomes of different exposure levels are unknown.
2. Implementing GLS models in R software package for known and unknown correlation structures between the outcomes.
3. Testing the relation between glucose levels and the risk of periodontal diseases by the means of proposed GLS models
Source of Data
Systematic reviews and data extraction are undertaken for the relation between glucose and periodontal disease. Another dataset from literature on the relation between alcohol and vascular disease data are also used to illustrate the application of the statistical method.
Results
1. Generalized least square method and restricted cubic splines model are applied to analyze the relation between glucose and periodontal disease: the increase in glucose level could lead to the increasing of the OR of the periodontal disease.
2. Fixed effects and random effects generalized least square method implemented in R yields the same results obtained by using the software package Stata or SAS.
3. The result obtained by fixing the correlations between log(OR) of the exposure level at 0.5, is very similar to those obtained by the actual number of the cases and controls.
Conclusions
The generalized least squares method proposed by Greenland and Longnecker requires the input of the correlations of the log(OR) between the exposure level rank when pooling the results, and the restricted cubic splines model proposed by Orsini can efficiently estimate the nonlinear relationship between the dose and response. Researchers can gain a greater sample size using our approach.
en
dc.description.provenanceMade available in DSpace on 2021-06-16T07:05:48Z (GMT). No. of bitstreams: 1
ntu-103-R01849011-1.pdf: 4405804 bytes, checksum: 3df4f1563848317ac1d6a2eb6ad19d5e (MD5)
Previous issue date: 2014
en
dc.description.tableofcontents論文口試委員審定書
誌謝 i
摘要 ii
Abstract iv
目錄 vi
圖表目錄 vii
第一章 前言 1
1.1 研究背景 1
1.2 研究目的 2
第二章 文獻回顧 3
2.1 Greenland與Longnecker 提出之GLS方法之回顧 3
2.2 利用統計軟體Stata進行GLS的操作 6
2.3 Pool-first與pool-last做法之間的差異 9
第三章 研究方法之劑量與效應反應的統合分析 10
3.1 資料來源 10
3.2 R程式上應用GLS基於'pool-first'的做法 14
3.3 R程式上應用GLS基於'pool-last'的做法 16
3.4 相關係數的彈性設定對於劑量與效應的統合估計之比較 17
第四章 結果 18
4.1 血糖與牙周病之間的關係結果呈現 18
4.2 Pool-first在R上的結果呈現 24
4.3 Pool-last在R上的結果呈現 26
4.4 相關係數的設定對於估計值之結果呈現 28
4.4.1將相關係數均設定成0.5在pool-first估計上之結果 28
4.4.2相關係數之彈性設定在pool-first估計上之結果 30
4.4.3將相關係數均設定成0.5在pool-last估計上之結果 32
第五章 討論 33
第六章 結論 36
第七章 參考文獻 37
第八章 附錄 41
dc.language.isozh-TW
dc.subject統合分析zh_TW
dc.subject牙周病zh_TW
dc.subject血糖zh_TW
dc.subject糖尿病zh_TW
dc.subjectperiodontal diseaseen
dc.subjectglucoseen
dc.subjectdiabetesen
dc.subjectmeta-analysisen
dc.title劑量與效應反應的統合分析之改良與應用:以血糖值與牙周病的關係為例zh_TW
dc.titleImprovement and application of dose-response meta-analysis to the relation between glucose and periodontal diseaseen
dc.typeThesis
dc.date.schoolyear102-2
dc.description.degree碩士
dc.contributor.oralexamcommittee簡國龍(Kuo-Liong Chien),季麟揚(Lin-Yang Chi)
dc.subject.keyword牙周病,血糖,糖尿病,統合分析,zh_TW
dc.subject.keywordperiodontal disease,glucose,diabetes,meta-analysis,en
dc.relation.page47
dc.rights.note有償授權
dc.date.accepted2014-07-10
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
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