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Target accrual not met
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Metabolic syndrome (MetS) is a cluster of metabolic conditions associated with obesity that predispose individuals to coronary heart diseases and diabetes but obesity has been shown to increase the risks of other diseases like cancer and asthma. Studies have also shown that obesity increases the risk of severe influenza infection and associated death and reduces the efficacy of influenza vaccine in the obese population but yet, the molecular mechanisms have not been described. The investigators are thus hypothesizing that differences in the innate immune responses between individual with or without metabolic syndrome impact viral infection and vaccine outcome. The investigators will perform seasonal influenza vaccination in people with or without metabolic syndrome to determine if the late adaptive response assessed by antibodies titers is different between the two groups and correlates with the early immune response assessed by gene expression profile in whole blood cells. The project proposed by the investigators will contribute to a better understanding of the inflammatory phenotype associated with metabolic syndrome and establish for the first time if it affects the immune protection against infectious diseases and particularly against influenza virus infection. The results will be important to determine if the population affected by metabolic syndrome should receive anti-influenza treatment in priority in the context of a severe influenza epidemic.
The development of industrialization with increased food consumption and sedentarity has given rise to an obesity pandemic, which affects up to 30% of the population in countries like US, these populations being at greater risk for cardiovascular diseases, and diabetes. More than obesity per se, visceral obesity is associated with metabolic diseases that cluster together and clinically defined metabolic syndrome. MetS comprises individuals with at least three of the 5 of the following factors: abdominal obesity, high blood triglycerides, low HDL ("good cholesterol"), high blood pressure and elevated fasting glucose. Metabolic syndrome is associated with a low-grade inflammation characterized by an infiltration of immune cells particularly in the adipose tissue, the liver and the pancreas that is thought to be responsible for the induction of insulin resistance. It is thought that obesity predisposes to other diseases such as cancer, asthma but only little attention has been given to infectious diseases. Studies have shown that obesity increases the risk of severe influenza infection and associated death and reduces the efficacy of influenza vaccine in the obese population but yet, the molecular mechanisms have not been described. Immune dysfunctions associated with obesity are suspected to play a major role but obesity is often associated with respiratory disorders that could directly explain the increased susceptibility to influenza infection. Also, metabolically healthy obesity is less associated with inflammation. Therefore, the investigators would like to focus particularly on metabolic syndrome, and determine how it influences immune response to viruses.
The investigators are thus hypothesizing that differences in the innate immune responses between individual with or without metabolic syndrome impact viral infection and vaccine outcome. Recent studies involving complex biological analysis and computational modeling have shown that the ability of an individual to positively respond to influenza vaccine can be molecularly predicted by looking at markers in the blood cells. The investigators will perform seasonal influenza vaccination in people with or without metabolic syndrome to determine if the late adaptive response assessed by antibodies titers is different between the two groups and correlates with the early immune response assessed by gene expression profile in whole blood cells.
Healthy nutritional habits along with increased physical activities should be best at preventing the development of metabolic syndrome but socio-economical issues are slowing the implementation of these changes. Therefore, as metabolic syndrome is raising public health concerns, it is important to understand why the metabolic syndrome affects susceptibility to diseases.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Influenza vaccine in metabolic syndrome | Experimental | Influenza vaccine |
|
| Influenza vaccine in healthy controls | Experimental | Influenza vaccine |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Influenza vaccine | Biological | Influenza vaccine administered intramuscularly (IM), 1 time only, on visit 3 |
|
| Measure | Description | Time Frame |
|---|---|---|
| Antibody Response D28 | Measured by hemagglutination inhibition assay | 28 days after vaccination compare to baseline (screening visit 1) pre-vaccination |
| Measure | Description | Time Frame |
|---|---|---|
| Gene Expression Profiling D1 | Analyze by RNA-seq | 1 day post-vaccination compare to baseline (gene expression screening visit #1 and study visit #1 D0 of vaccination) |
| Gene Expression Profiling D28 |
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Inclusion criteria for the METABOLIC SYNDROME COHORT( Participants must have 3 or more of the following 5 risk factors):
Inclusion criteria for the HEALTHY CONTROLS (Participants must have all of the requirements below) :
Exclusion criteria :
Study Population Description The population from which the groups will be selected are resident of New York City.
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| Name | Affiliation | Role |
|---|---|---|
| Ursula Andreo, PhD | The Rockefeller University Center for Clinical and Translational | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Rockefeller University | New York | New York | 10065 | United States |
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Pre-screening took place along with a two-step screening visit for eligibility criteria. Those not meeting eligibility would screen out: 86 prescreened, 28 initial contact for screening.
Advertising and Research Volunteer Repository Database
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| ID | Title | Description |
|---|---|---|
| FG000 | Influenza Vaccine in Metabolic Syndrome | Influenza vaccine Influenza vaccine: Influenza vaccine administered intramuscularly (IM), 1 time only, on visit 3 |
| FG001 | Influenza Vaccine in Healthy Controls | Influenza vaccine Influenza vaccine: Influenza vaccine administered intramuscularly (IM), 1 time only, on visit 3 |
| Title | Milestones | Reasons Not Completed | |||||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Overall Study |
|
|
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| ID | Title | Description |
|---|---|---|
| BG000 | Influenza Vaccine in Metabolic Syndrome | Influenza vaccine Influenza vaccine: Influenza vaccine administered intramuscularly (IM), 1 time only, on visit 3 |
| BG001 | Influenza Vaccine in Healthy Controls |
| Units | Counts |
|---|---|
| Participants |
|
| Title | Description | Population Description | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Denominator Units Selected | Denominators | Classes |
|---|---|---|---|---|---|---|---|---|---|
| Age, Categorical | Count of Participants |
| Type | Title | Description | Population Description | Reporting Status | Anticipated Posting Date | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Time Frame | Units Analyzed | Denominator Units Selected | Arm/Group Information | Denominators | Classes | Analyses | |||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Primary | Antibody Response D28 | Measured by hemagglutination inhibition assay | Data were not collected | Posted | 28 days after vaccination compare to baseline (screening visit 1) pre-vaccination |
|
Adverse event information collected from time of enrollment through completion of study visits, 3 months.
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| ID | Title | Description | Deaths (Affected) | Deaths (At Risk) | Serious Events (Affected) | Serious Events (At Risk) | Other Events (Affected) | Other Events (At Risk) |
|---|---|---|---|---|---|---|---|---|
| EG000 | Influenza Vaccine in Metabolic Syndrome | Influenza vaccine Influenza vaccine: Influenza vaccine administered intramuscularly (IM), 1 time only, on visit 3 |
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| Term | Organ System | Source Vocabulary | Assessment Type | Notes | Statistical Information |
|---|---|---|---|---|---|
| infections and infestations: upper respiratory infection: skin infection | Skin and subcutaneous tissue disorders | CTCAE v4.0 | Non-systematic Assessment | Dog bite on left great toe. Family pet with "all immunizations". Neosporin oint daily and band aid. Ambulatory and comfortable. No redness, swelling, drainage or tenderness. It is healing well. |
Inclusion Criteria hard to meet among population: many individuals do not self-identify as having metabolic syndrome, participants must have untreated metabolic syndrome. Challenges led to early termination with sample size not being attainable.
| Title | Organization | Phone | Extension | |
|---|---|---|---|---|
| Dr. Ursula Andreo | Rockefeller University | 212-327-7894 | uandreo@gmail.com |
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| Type | Includes Protocol | Includes SAP | Includes ICF | Document Label | Document Date | Document Uploaded Date | Document File Name |
|---|---|---|---|---|---|---|---|
| Prot_SAP | Yes | Yes | No | Study Protocol and Statistical Analysis Plan | May 7, 2017 | Sep 1, 2017 | Prot_SAP_000.pdf |
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| ID | Term |
|---|---|
| D007153 | Immunologic Deficiency Syndromes |
| D024821 | Metabolic Syndrome |
| ID | Term |
|---|---|
| D007154 | Immune System Diseases |
| D007333 | Insulin Resistance |
| D006946 | Hyperinsulinism |
| D044882 | Glucose Metabolism Disorders |
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| ID | Term |
|---|---|
| D007252 | Influenza Vaccines |
| ID | Term |
|---|---|
| D014765 | Viral Vaccines |
| D014612 | Vaccines |
| D001688 | Biological Products |
| D045424 | Complex Mixtures |
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Analyze by RNA-seq
| 28 days post-vaccination compare to baseline (gene expression screening visit #1 and study visit #1 D0 of vaccination) |
| Gene Expression Profiling D90 | Analyze by RNA-seq | 90 days post-vaccination compare to baseline (gene expression screening visit #1 and study visit #1 D0 of vaccination) |
| Antibody Response D90 | Measured by hemagglutination inhibition assay | 90 days after vaccination compare to day 28 |
Influenza vaccine
Influenza vaccine: Influenza vaccine administered intramuscularly (IM), 1 time only, on visit 3
| BG002 | Total | Total of all reporting groups |
| Participants |
|
| Sex: Female, Male | Count of Participants | Participants |
|
| Race and Ethnicity Not Collected | Race and Ethnicity were not collected from any participant. | Count of Participants | Participants |
|
| Region of Enrollment | Number | participants |
|
| Units | Counts |
|---|---|
| Participants |
|
| Secondary | Gene Expression Profiling D1 | Analyze by RNA-seq | Data were not collected. | Posted | 1 day post-vaccination compare to baseline (gene expression screening visit #1 and study visit #1 D0 of vaccination) |
|
|
| Secondary | Gene Expression Profiling D28 | Analyze by RNA-seq | Data were not collected. | Posted | 28 days post-vaccination compare to baseline (gene expression screening visit #1 and study visit #1 D0 of vaccination) |
|
|
| Secondary | Gene Expression Profiling D90 | Analyze by RNA-seq | Data were not collected. | Posted | 90 days post-vaccination compare to baseline (gene expression screening visit #1 and study visit #1 D0 of vaccination) |
|
|
| Secondary | Antibody Response D90 | Measured by hemagglutination inhibition assay | Data were not collected. | Posted | 90 days after vaccination compare to day 28 |
|
|
| 0 |
| 3 |
| 0 |
| 3 |
| 1 |
| 3 |
| EG001 | Influenza Vaccine in Healthy Controls | Influenza vaccine Influenza vaccine: Influenza vaccine administered intramuscularly (IM), 1 time only, on visit 3 | 0 | 2 | 0 | 2 | 1 | 2 |
|
| gastrointestinal disorders: dyspepsia | Gastrointestinal disorders | CTCAE v4.0 | Non-systematic Assessment | moderate to severe indigestion after eating brunch. Denies vomiting, diarrhea, sweats or fever. Self treated with pepto bismol with relief. Has history of self-diagnosed gastroesophageal reflux disease (GERD). |
|
| gastrointestinal disorders: diarrhea | Gastrointestinal disorders | CTCAE v4.0 | Non-systematic Assessment | Subject experienced abdominal cramping and diarrhea after eating food from a street vendor. No fever, no vomiting, was able to eat and drink. Onset 3 days after receiving flu vaccine. Symptoms resolved after 48 hours. |
|
| Upper Respiratory | Respiratory, thoracic and mediastinal disorders | CTCAE v4.0 | Non-systematic Assessment | Subject called complaining of congestion and cough. |
|
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| D008659 |
| Metabolic Diseases |
| D009750 | Nutritional and Metabolic Diseases |