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Genomic and Co-Evolutionary Determinants of Clinical Severity in Active Tuberculosis Patients- [electronic resource]
ข้อมูลเนื้อหา
Genomic and Co-Evolutionary Determinants of Clinical Severity in Active Tuberculosis Patients- [electronic resource]
자료유형  
 학위논문
Control Number  
0016935486
International Standard Book Number  
9798380198677
Dewey Decimal Classification Number  
610
Main Entry-Personal Name  
McHenry, Michael.
Publication, Distribution, etc. (Imprint  
[S.l.] : Case Western Reserve University., 2021
Publication, Distribution, etc. (Imprint  
Ann Arbor : ProQuest Dissertations & Theses, 2021
Physical Description  
1 online resource(129 p.)
General Note  
Source: Dissertations Abstracts International, Volume: 85-03, Section: B.
General Note  
Advisor: Bush, William.
Dissertation Note  
Thesis (Ph.D.)--Case Western Reserve University, 2021.
Restrictions on Access Note  
This item must not be sold to any third party vendors.
Summary, Etc.  
요약Tuberculosis (TB) is a major public health problem, causing more deaths globally than any other pathogen prior to COVID19. It is also the leading cause of death among people infected with human immunodeficiency virus (HIV). Susceptibility to TB can be influenced by human genetic variation. However, factors underlying variation in TB severity are less well studied. Clinical severity is an important phenotype that encompasses prognosis, patient experience, and risk of mortality. Thus, it is important to study severity, as it can help us better understand patients' quality of life, disease experience, and to predict survival among TB patients receiving treatment. There is also evidence that MTB genetic variation as delineated by phylogenetic lineage can affect TB disease severity, when considered simultaneously with human genetic variations and the interaction between the two. Many genetic studies of TB stop short of linking these genetic effects to biological function. The proposed study will address these fundamental gaps by 1) studying the genomic underpinnings of active TB severity using a meaningful, replicable, and validated clinical phenotype; 2) demonstrating evidence of co-evolution between humans and MTB on a population level how it affects severity; and 3) bridging the gap between genetic variants and immunological function by studying gene expression in the macrophage response. The overall goal is to examine how genomic variation in humans and MTB impact the immunological response to active TB disease and how this correlates with clinical severity.
Subject Added Entry-Topical Term  
Medicine.
Subject Added Entry-Topical Term  
Epidemiology.
Subject Added Entry-Topical Term  
Genetics.
Subject Added Entry-Topical Term  
Public health.
Index Term-Uncontrolled  
Tuberculosis
Index Term-Uncontrolled  
Genetic epidemiology
Index Term-Uncontrolled  
Infectious disease
Index Term-Uncontrolled  
Evolution
Index Term-Uncontrolled  
Immunological function
Added Entry-Corporate Name  
Case Western Reserve University Epidemiology and Biostatistics
Host Item Entry  
Dissertations Abstracts International. 85-03B.
Host Item Entry  
Dissertation Abstract International
Electronic Location and Access  
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Control Number  
joongbu:642911
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