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Purpose

In this study the investigators will incorporate a wide range of clinical variables associated with aging and cardiovascular disease to determine whether they are associated with mutation status independent of chronologic age. Clinically, aging can be operationalized using geriatric assessment, which entails a comprehensive multi-dimensional assessment of the health of an older adult, including measures of comorbidity, polypharmacy, functional status, cognition, depression, falls, social activities and social support. Given that aging is heterogeneous, geriatric assessment allows greater specificity for aging than chronological age alone.

Conditions

Eligibility

Eligible Ages
Over 50 Years
Eligible Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • At least 50 years of age. - Able to understand written and spoken English. - Able to understand and willing to sign an IRB-approved written informed consent document (or that of a legally authorized representative, if applicable for the trauma cohort)

Exclusion Criteria

  • Inability or unwillingness to complete health questionnaire. - History of a recent (<30 days) acute viral illness. - Current cancer diagnosis and currently receiving chemotherapy or undergoing radiation therapy. A prior history of cancer is allowed if the participant completed therapy > 1 year prior to enrollment; participants with a prior diagnosis of cancer will be asked to sign a release of information for the research team to obtain records regarding their prior cancer treatment. - Current use of drugs that cause DNA damage (e.g. Cytoxan, azathioprine, etc.) for the treatment of a non-malignant disease. - Vulnerable populations (e.g. prisoners). - Known infection with Hepatitis B or C, HTLV, or HIV. - Additional exclusion for optional bone marrow aspirate/biopsy substudy: - Use of medications for anticoagulation or "blood thinning" including warfarin, low molecular weight heparins (enoxaparin, daltaparin) or direct-acting oral anticoagulants (dabigatran, rivaroxaban, apixaban, edoxaban or betrixaban) - allergy to lidocaine or other local anesthetics.

Study Design

Phase
Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Arm Groups

ArmDescriptionAssigned Intervention
Arm A: Clonal hematopoiesis - Complete several self-administered health assessments at baseline and every 6 months until death. - Cognitive assessment, Gait Speed, grip strength, blood pressure, height, and weight will be performed by a member of the research team at baseline and every 6 months until death. - Peripheral blood draw will occur at baseline and no more than every 6 months until death. - Buccal swabs will occur at baseline and repeated as necessary, but not more than every 6 months until death - May be approached about optional bone marrow biopsy
  • Other: Cognitive Assessment
    -Baseline and no more frequently than every 6 months until death
  • Other: Activities of Daily Living Questionnaire
    - 10 items about daily functional status - Baseline and no more frequently than every 6 months until death
  • Other: Instrumental Activities of Daily Living, subscale of the OARS
    - 7 items about daily functional status - Baseline and no more frequently than every 6 months until death
  • Other: Karnofsky Self-reported Performance Rating Scale
    - 1 item about daily functional status - Baseline and no more frequently than every 6 months until death
  • Other: Number of Falls
    - 1 item about daily functional status - Baseline and no more frequently than every 6 months until death
  • Other: Physical Health Section, subscale of the OARS
    - 13 items about comorbidity - Baseline and no more frequently than every 6 months until death
  • Other: MOS Social Activity Survey
    - 4 items about social activity - Baseline and no more frequently than every 6 months until death
  • Other: Unintentional Weight Loss
    - 2 items about nutrition - Baseline and no more frequently than every 6 months until death
  • Genetic: Peripheral Blood Draw
    -Baseline and no more frequently than every 6 months until death
  • Genetic: Buccal Swab
    - Participants will rinse their mouths 2 times with water for 20-30 seconds and discard the expectorated sample. One side of the inner cheek (buccal mucosa) will then be scraped with a cotton swab 20 times (alternatively, the tongue will be brushed 20 times with a toothbrush) - Baseline and no more frequently than every 6 months until death
  • Other: Heart Health and Smoking History from BRFSS questionnaire
    - 7 items about heart health and smoking history - Baseline and no more frequently than every 6 months until death
  • Other: Gait Speed
    - Research coordinator will test gait speed - Baseline and no more frequently than every 6 months until death
  • Other: Grip Strength
    - Research coordinator will test grip strength - Baseline and no more frequently than every 6 months until death
  • Other: Height and Weight measurements
    -Baseline and no more frequently than every 6 months until death
  • Other: Blood pressure measurement
    -Baseline and no more frequently than every 6 months until death
  • Procedure: Optional bone marrow biopsy
    -1 optional bone marrow biopsy
Arm B: No clonal hematopoiesis - Complete several self-administered health assessments at baseline and every 6 months until death. - Cognitive assessment, Gait Speed, grip strength, blood pressure, height, and weight will be performed by a member of the research team at baseline and every 6 months until death. - Peripheral blood draw will occur at baseline and no more than every 6 months until death. - Buccal swabs will occur at baseline and repeated as necessary, but not more than every 6 months until death - May be approached about optional bone marrow biopsy
  • Other: Cognitive Assessment
    -Baseline and no more frequently than every 6 months until death
  • Other: Activities of Daily Living Questionnaire
    - 10 items about daily functional status - Baseline and no more frequently than every 6 months until death
  • Other: Instrumental Activities of Daily Living, subscale of the OARS
    - 7 items about daily functional status - Baseline and no more frequently than every 6 months until death
  • Other: Karnofsky Self-reported Performance Rating Scale
    - 1 item about daily functional status - Baseline and no more frequently than every 6 months until death
  • Other: Number of Falls
    - 1 item about daily functional status - Baseline and no more frequently than every 6 months until death
  • Other: Physical Health Section, subscale of the OARS
    - 13 items about comorbidity - Baseline and no more frequently than every 6 months until death
  • Other: MOS Social Activity Survey
    - 4 items about social activity - Baseline and no more frequently than every 6 months until death
  • Other: Unintentional Weight Loss
    - 2 items about nutrition - Baseline and no more frequently than every 6 months until death
  • Genetic: Peripheral Blood Draw
    -Baseline and no more frequently than every 6 months until death
  • Genetic: Buccal Swab
    - Participants will rinse their mouths 2 times with water for 20-30 seconds and discard the expectorated sample. One side of the inner cheek (buccal mucosa) will then be scraped with a cotton swab 20 times (alternatively, the tongue will be brushed 20 times with a toothbrush) - Baseline and no more frequently than every 6 months until death
  • Other: Heart Health and Smoking History from BRFSS questionnaire
    - 7 items about heart health and smoking history - Baseline and no more frequently than every 6 months until death
  • Other: Gait Speed
    - Research coordinator will test gait speed - Baseline and no more frequently than every 6 months until death
  • Other: Grip Strength
    - Research coordinator will test grip strength - Baseline and no more frequently than every 6 months until death
  • Other: Height and Weight measurements
    -Baseline and no more frequently than every 6 months until death
  • Other: Blood pressure measurement
    -Baseline and no more frequently than every 6 months until death
  • Procedure: Optional bone marrow biopsy
    -1 optional bone marrow biopsy
Arm C: No clonal hematopoiesis & no follow-up - Complete several self-administered health assessments at baseline with no further follow-up - Cognitive assessment, Gait Speed, grip strength, blood pressure, height, and weight will be performed by a member of the research team at baseline with no further follow-up - Peripheral blood draw will occur at baseline with no further follow-up - Buccal swabs will occur at baseline with no further follow-up
  • Other: Cognitive Assessment
    -Baseline and no more frequently than every 6 months until death
  • Other: Activities of Daily Living Questionnaire
    - 10 items about daily functional status - Baseline and no more frequently than every 6 months until death
  • Other: Instrumental Activities of Daily Living, subscale of the OARS
    - 7 items about daily functional status - Baseline and no more frequently than every 6 months until death
  • Other: Karnofsky Self-reported Performance Rating Scale
    - 1 item about daily functional status - Baseline and no more frequently than every 6 months until death
  • Other: Number of Falls
    - 1 item about daily functional status - Baseline and no more frequently than every 6 months until death
  • Other: Physical Health Section, subscale of the OARS
    - 13 items about comorbidity - Baseline and no more frequently than every 6 months until death
  • Other: MOS Social Activity Survey
    - 4 items about social activity - Baseline and no more frequently than every 6 months until death
  • Other: Unintentional Weight Loss
    - 2 items about nutrition - Baseline and no more frequently than every 6 months until death
  • Genetic: Peripheral Blood Draw
    -Baseline and no more frequently than every 6 months until death
  • Genetic: Buccal Swab
    - Participants will rinse their mouths 2 times with water for 20-30 seconds and discard the expectorated sample. One side of the inner cheek (buccal mucosa) will then be scraped with a cotton swab 20 times (alternatively, the tongue will be brushed 20 times with a toothbrush) - Baseline and no more frequently than every 6 months until death
  • Other: Heart Health and Smoking History from BRFSS questionnaire
    - 7 items about heart health and smoking history - Baseline and no more frequently than every 6 months until death
  • Other: Gait Speed
    - Research coordinator will test gait speed - Baseline and no more frequently than every 6 months until death
  • Other: Grip Strength
    - Research coordinator will test grip strength - Baseline and no more frequently than every 6 months until death
  • Other: Height and Weight measurements
    -Baseline and no more frequently than every 6 months until death
  • Other: Blood pressure measurement
    -Baseline and no more frequently than every 6 months until death
Arm D: Hip replacement - Complete several self-administered health assessments at baseline and every 6 months until death. - Cognitive assessment, Gait Speed, grip strength, blood pressure, height, and weight will be performed by a member of the research team at baseline and every 6 months until death. - Participants with or without clonal hematopoiesis who are undergoing hip replacement - Peripheral blood draw will occur at baseline and no more than every 6 months until death. - Buccal swabs will occur at baseline and repeated as necessary, but not more than every 6 months until death - May be approached about optional bone marrow biopsy
Arm E: Trauma -Blood sample at the time of admission with initial bloodwork. For inpatient participants, weekly follow-up samples will be drawn with morning phlebotomy. A follow-up sample collection will occur 4-7 weeks after discharge.
  • Procedure: Blood draw for trauma measurements
    -For Arm E only

Recruiting Locations

Washington University in St. Louis and nearby locations

Washington University School of Medicine
St Louis 4407066, Missouri 4398678 63110
Contact:
Meagan Jacoby, M.D.
314-747-8439
mjacoby@wustl.edu

More Details

NCT ID
NCT02604563
Status
Recruiting
Sponsor
Washington University School of Medicine

Study Contact

Meagan Jacoby, M.D.
314-747-8439
mjacoby@wustl.edu

Notice

Study information shown on this site is derived from ClinicalTrials.gov (a public registry operated by the National Institutes of Health). The listing of studies provided is not certain to be all studies for which you might be eligible. Furthermore, study eligibility requirements can be difficult to understand and may change over time, so it is wise to speak with your medical care provider and individual research study teams when making decisions related to participation.