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As population aging accelerates, infectious diseases have become a major factor affecting the health, quality of life, and survival outcomes of older adults. Immunosenescence, chronic low-grade inflammation (inflammaging), and dysbiosis of the respiratory and gut microbiota are considered important mechanisms underlying increased susceptibility to infection and a higher risk of severe disease in older adults. However, the interactions among these factors and their impact on infection-related outcomes remain incompletely understood.
Building upon a previously established pilot cohort of older adults, this study aims to further identify and validate key biological characteristics and risk factors associated with infectious diseases through large-scale population follow-up. A large prospective cohort of older adults will be established, while retrospective healthcare data collected since 2019 will also be integrated. Demographic information, comorbidities, medication history, infection-related clinical data, and biological specimens, including blood, urine, fecal, and respiratory samples, will be collected for long-term longitudinal follow-up. By integrating immunological assessments, immune repertoire analyses, microbiome profiling, and other multi-omics technologies, this study will systematically evaluate the effects of immunosenescence, respiratory and gut microbiome alterations, and environmental and climatic factors on the occurrence, severity, and prognosis of infectious diseases in older adults. The study aims to identify key biomarkers and microbial signatures associated with infection risk and to develop risk prediction and early warning models for infectious diseases in older adults, thereby providing scientific evidence for precision prevention, optimized clinical management, and public health decision-making in aging populations.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Older Adults Without Infection | Community-dwelling adults aged 60 years and older who do not develop any clinically diagnosed infectious disease during the follow-up period. | ||
| Older Adults With Infection | Community-dwelling adults aged 60 years and older who develop clinically diagnosed infectious diseases during follow-up. |
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| Measure | Description | Time Frame |
|---|---|---|
| Occurrence of infectious disease outcomes in older adults | Occurrence of infectious disease outcomes in older adults, including all-cause mortality, infection-related mortality, first infectious disease event, and progression to severe infection. | Baseline to 3 years |
| Measure | Description | Time Frame |
|---|---|---|
| High-Frequency Infection Status (≥6 Infections per Year) | Defined as an average of six or more infectious episodes per year during follow-up. | Baseline to 3 Years |
| Pathogen-Specific Infection Events |
| Measure | Description | Time Frame |
|---|---|---|
| Changes in Metabolomic and Microbiome Profiles | Assessment of longitudinal changes in metabolomic profiles and gut and respiratory microbiome characteristics associated with infection risk and disease severity. | Baseline to 3 Years |
Inclusion Criteria:
- General Cohort Inclusion Criteria
Infection Cohort Inclusion Criteria
Exclusion Criteria:
General Cohort Exclusion Criteria
Infection Cohort Exclusion Criteria
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Adults aged 60 years and older
| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Jingwen Ai | Contact | 17317958269 | jingwenai1990@126.com |
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Infectious disease events caused by specific pathogens, used to evaluate pathogen distribution and temporal trends.
| Baseline to 3 Years |
| Changes in Immune Function Biomarkers | Assessment of longitudinal changes in immune cell subsets and immune function status. | Baseline to 3 Years |
| ID | Term |
|---|---|
| D003141 | Communicable Diseases |
| ID | Term |
|---|---|
| D007239 | Infections |
| D020969 | Disease Attributes |
| D010335 | Pathologic Processes |
| D013568 | Pathological Conditions, Signs and Symptoms |
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