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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/123456789/99857
完整後設資料紀錄
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dc.contributor.advisor簡國龍zh_TW
dc.contributor.advisorKuo-Liong Chienen
dc.contributor.author許瑞云zh_TW
dc.contributor.authorJui-Yun Hsuen
dc.date.accessioned2025-09-19T16:06:40Z-
dc.date.available2025-09-20-
dc.date.copyright2025-09-19-
dc.date.issued2025-
dc.date.submitted2025-07-07-
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dc.identifier.urihttp://tdr.lib.ntu.edu.tw/jspui/handle/123456789/99857-
dc.description.abstract目的:分析發炎生物指標,如白血球總數及其分類、白細胞介素-6、C反應蛋白與台灣族群第二型糖尿病盛行率的關聯,找出在第二型糖尿病風險評估中最具實用性與參考價值的發炎生物指標。

方法:使用台灣老人健康之社會因素與生物指標研究 (Social Environment and Biomarkers of Aging Study, SEBAS) 資料進行橫斷性研究。第二型糖尿病依據血液檢查結果、用藥情況、以及自述資料定義。分析採用羅吉斯回歸模型估算與第二型糖尿病的勝算比,並運用樣條模型 (restricted cube spline models) 分析其關係型態。次群體分析用以探討潛在風險因子的效應修飾,並用重分類改善指標淨值 (net reclassification improvement, NRI) 與整合性鑑別度改善指數 (integrated discrimination improvement, IDI) 評估各模型的辨別能力。

結果:在 1,402 位參與者中,較高的白血球總數與第二型糖尿病盛行率風險顯著相關 (勝算比 = 2.56,95%信賴區間:1.72-3.81;趨勢檢定:P < 0.001),其次為嗜中性球、淋巴球、白細胞介素-6及C反應蛋白。僅有白細胞介素-6與第二型糖尿病盛行率之間呈非線性關係,為飽和曲線的型態。此外,次群體分析顯示,白血球數與第二型糖尿病的關係在非吸菸者中較強 (交互作用P值 = 0.010),而C反應蛋白的關聯則在有規律運動者中較為明顯 (交互作用P值 = 0.024)。最後,綜合曲線下面積 (AUC)、重分類改善指標淨值 (NRI) 與整合性鑑別度改善指數 (IDI),白血球數在各發炎指標中展現出最佳的辨別能力。

結論:在台灣族群中,較高數值的白血球、嗜中性球、淋巴球、白細胞介素-6、C反應蛋白與第二型糖尿病的盛行率具有顯著關聯。其中,白血球數展現出最強的辨別能力,有助於臨床醫師識別高風險案例並及早介入。
zh_TW
dc.description.abstractObjective: To identify the most practical and informative inflammatory biomarker associated with type 2 diabetes risk in the Taiwanese population, we examined the relationships between various biomarkers, including WBC count and its differentials, IL-6, and hs-CRP, and the prevalence of type 2 diabetes.

Methods: We conducted a cross-sectional study using data from the Social Environment and Biomarkers of Aging Study (SEBAS). Type 2 diabetes was defined based on results from blood tests, medication use, and self-reported information. Odds ratios for type 2 diabetes were calculated using logistic regression models, and restricted cubic spline models were applied to understand the relationship pattern. The subgroup analyses examined effect modification by potential risk factors, and discrimination was compared using the net reclassification improvement (NRI) and integrated discrimination improvement (IDI) approaches.

Results: Among 1,402 participants, higher WBC count was significantly associated with type 2 diabetes risk (odds ratio = 2.56, 95% confidence interval: 1.72-3.81; P for trend < 0.001), followed by neutrophils, lymphocytes, IL-6, and hs-CRP. Only IL-6 exhibited a nonlinear relationship with a saturation curve regarding the prevalence of type 2 diabetes. Furthermore, subgroup analyses revealed that the association between WBC count and type 2 diabetes was stronger among nonsmokers (P for interaction = 0.010), while the association for hs-CRP was more pronounced among individuals with regular exercise habits (P for interaction = 0.024). Lastly, WBC count demonstrated the best discriminatory performance based on AUC, NRI, and IDI.

Conclusion: Elevated levels of WBC, neutrophils, lymphocytes, IL-6, and hs-CRP were significantly associated with the prevalence of type 2 diabetes in the Taiwanese population. Among these biomarkers, WBC demonstrated the strongest discriminatory ability, potentially assisting clinicians in identifying high-risk individuals and initiating early interventions.
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dc.description.tableofcontents口試委員會審定書 i
誌謝 iii
中文摘要及關鍵詞 iv
Abstract and keywords v
Abbreviation vii
Table of contents viii
List of Figures x
List of Tables xi
Chapter 1 Introduction 1
1.1 Type 2 diabetes 1
1.2 Risk factors 3
1.3 Inflammation 4
1.3.1 White blood cell count and differential counts 4
1.3.2 Interleukin-6 (IL-6) 6
1.3.3 C-reactive protein (CRP) 9
1.4 Biological mechanism 11
1.5 Research gaps 13
Chapter 2 Hypothesis and aims 14
Chapter 3 Materials and methods 15
3.1 Study design and population 15
3.2 Assessment of inflammation biomarkers 16
3.3 Definition of type 2 diabetes cases 18
3.4 Covariates 19
3.5 Statistical analysis 20
3.5.1 Descriptive analysis 20
3.5.2 Logistic regression models 21
3.5.3 Restricted cubic spline models 22
3.5.4 Subgroup analysis 23
3.5.5 Discrimination ability 23
3.5.6 Sensitivity analysis 25
3.5.7 Sample size and power calculation 26
3.5.8 Software 26
3.6 Ethnical consideration 27
Chapter 4 Results 28
4.1 Characteristics of study population 28
4.1.1 Distribution of characteristics by quartiles of WBC and differential counts 28
4.1.2 Distribution of characteristics by quartiles of IL-6 and hs-CRP 29
4.2 The relationship between biomarkers and the prevalence of type 2 diabetes 30
4.3 Restricted cubic spline models 32
4.4 Subgroup analysis 33
4.5 Discrimination ability 34
4.5 Sensitivity analysis 35
Chapter 5 Discussion 36
5.1 Main findings 36
5.2 Comparing with previous studies 36
5.2.1 Associations between WBC, differential counts, and type 2 diabetes 36
5.2.2 Associations between IL-6 and type 2 diabetes 40
5.2.3 Associations between hs-CRP and type 2 diabetes 41
5.3 Biological mechanism 42
5.4 Clinical implications 45
5.5 Strengths and limitations 46
Chapter 6 Conclusion 48
Reference 49
Appendix 96
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dc.language.isoen-
dc.subject白細胞介素-6zh_TW
dc.subject白血球計數zh_TW
dc.subject第二型糖尿病zh_TW
dc.subject發炎zh_TW
dc.subject辨別能力zh_TW
dc.subjectC反應蛋白zh_TW
dc.subject白血球分類zh_TW
dc.subjectWhite blood counten
dc.subjectInterleukin-6en
dc.subjectInflammationen
dc.subjectDiscrimination abilityen
dc.subjectC-reactive proteinen
dc.subjectType 2 diabetesen
dc.subjectWhite blood cell differentialen
dc.title台灣中老年族群發炎指標與第二型糖尿病危險之關係: 以SEBAS資料庫族群之橫斷性研究zh_TW
dc.titleAssociation between Inflammatory Biomarkers and the Risk of Type 2 Diabetes in Middle-aged and Elderly Adults in Taiwan: a Cross-sectional Study from SEBASen
dc.typeThesis-
dc.date.schoolyear113-2-
dc.description.degree碩士-
dc.contributor.oralexamcommittee林宇旋;吳泓彥;石見拓zh_TW
dc.contributor.oralexamcommitteeYu-Hsuan Lin;Hon-Yen Wu;Taku Iwamien
dc.subject.keywordC反應蛋白,辨別能力,發炎,白細胞介素-6,第二型糖尿病,白血球計數,白血球分類,zh_TW
dc.subject.keywordC-reactive protein,Discrimination ability,Inflammation,Interleukin-6,Type 2 diabetes,White blood count,White blood cell differential,en
dc.relation.page101-
dc.identifier.doi10.6342/NTU202501622-
dc.rights.note未授權-
dc.date.accepted2025-07-09-
dc.contributor.author-college公共衛生學院-
dc.contributor.author-dept流行病學與預防醫學研究所-
dc.date.embargo-liftN/A-
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