SSRI's and the Rate of Progression From MCI to Dementia

Sponsor
Ohio State University (Other)
Overall Status
Recruiting
CT.gov ID
NCT04901494
Collaborator
(none)
200
1
10
20.1

Study Details

Study Description

Brief Summary

This trial is investigating if serotonin reuptake inhibitor (SSRI) use in Mild Cognitive Impairment (MCI) patients will lead to a lower rate of progression to dementia.

It's hypothesized that patients treated with an SSRI at the time of MCI diagnosis, without evidence of an active primary psychiatric condition other than neurocognitive disorder, will have a lower rate of progression to Alzheimer's disease dementia or to other types of dementia.

Condition or Disease Intervention/Treatment Phase

Detailed Description

Whether SSRIs affect the progression of MCI to dementia is not well studied with longitudinal prospectively collected date. Any decrease in the incidence of the progression of MCI to Alzheimer's dementia would be beneficial to patients.

This trial is investigating if serotonin reuptake inhibitor (SSRI) use in Mild Cognitive Impairment (MCI) patients will lead to a lower rate of progression to dementia.

This is a retrospective study of prospectively collected longitudinal data in patients followed at the Cognitive and Memory Disorders Center from 2010-2019. There are 3 arms: (1) subjects with an initial diagnosis of MCI who were treated with an SSRI for at least one year prior to the diagnosis of MCI (2) subjects with an initial diagnosis of MCI who were started on an SSRI at the time of diagnosis and treated with it for at least 6 months after the diagnosis of MCI and (3) subjects without SSRI use.

All the subjects have been evaluated based on a comprehensive standardized evaluation for the initial diagnosis and follow up over time. Chart reviews will be conducted on newly diagnosed MCI patients from 2010-2016 who have at least 2 years of annual follow up documented in their electronic medical record. Follow up visit notes through 2019 will be included in the review.

Study Design

Study Type:
Observational
Anticipated Enrollment :
200 participants
Observational Model:
Cohort
Time Perspective:
Retrospective
Official Title:
Impact of SSRIs on the Rate of Progression of Patients With Mild Cognitive Impairment to Alzheimer's Disease Dementia and Other Neurodegenerative Dementias, With or Without Concurrent Use of Acetylcholinesterase Inhibitors
Actual Study Start Date :
Sep 1, 2021
Anticipated Primary Completion Date :
Jul 1, 2022
Anticipated Study Completion Date :
Jul 1, 2022

Arms and Interventions

Arm Intervention/Treatment
SSRI for at least one year prior to the diagnosis of MCI

subjects with an initial diagnosis of MCI who were treated with an SSRI for at least one year prior to the diagnosis of MCI

Drug: SSRI
Selective serotonin reuptake inhibitor
Other Names:
  • Selective serotonin reuptake inhibitor
  • SSRI at the time of diagnosis and treated with it for at least 6 months after the diagnosis of MCI

    SSRI at the time of diagnosis and treated with it for at least 6 months after the diagnosis of MCI

    Drug: SSRI
    Selective serotonin reuptake inhibitor
    Other Names:
  • Selective serotonin reuptake inhibitor
  • Subjects without SSRI use

    Subjects without SSRI use

    Outcome Measures

    Primary Outcome Measures

    1. SSRI rate of progression to dementia [2010-2019]

      1.To determine if subjects treated with an SSRI for at least one year prior to the diagnosis of MCI or at least 6 months after the diagnosis of MCI will (a) have a lower rate of progression to Alzheimer's disease dementia or (b) have a lower rate of progression to other dementia conditions (i.e. Lewy Body Dementia, Frontotemporal Dementia, Vascular Dementia, Normal Pressure Hydrocephalus, Parkinson Disease Dementia… etc) compared to subjects who are not treated with an SSRI.

    2. SSRI and acetylcholinesterase inhibitor use progression to dementia [2010-2019]

      2.To determine if SSRI use in combination with acetylcholinesterase inhibitor use will affect the rate of progression to dementia.

    Secondary Outcome Measures

    1. Rate of conversion from MCI to dementia and the other factors [2010-2019]

      1. To investigate correlations between the rate of conversion from MCI to dementia and other factors.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    50 Years and Older
    Sexes Eligible for Study:
    All
    Inclusion Criteria:
    1. Age 55+

    2. Diagnosis of mild cognitive impairment.

    3. One year treatment with an SSRI prior to diagnosis of MCI or six months treatment after diagnosis of MCI for the intervention groups. No treatment with an SSRI prior to the diagnosis of MCI or after the diagnosis of MCI for the control group.

    4. A minimum of two annual follow up evaluations.

    Exclusion Criteria:
    1. Patients with CNS infection or inflammation

    2. HIV

    3. Syphilis

    4. Patients with poorly controlled Epilepsy based on the opinion of the investigator.

    5. Patients with space occupying lesions of the brain (glioma, meningioma, brain metastasis).

    6. Patients with systemic inflammatory condition or cancer undergoing chemotherapy or on chronic immune modulatory treatments.

    7. Blind patients that were not able to complete a cognitive assessment.

    8. Patients with chronic pain who are on excluded pain medications.

    9. Patients with Attention Deficit Disorder that require the use of stimulant medications.

    10. Patients with Traumatic Brain Injury.

    11. Patients with Cerebral Aneurysm Rupture.

    12. Patients with chronic psychiatric conditions, unless in remission. Recurrent chronic psychiatric condition in relapse, chronic recurrent Major Depression in relapse, chronic recurrent bipolar disorder, chronic relapsing schizoaffective disorder and chronic recurrent anxiety disorder requiring chronic use of benzodiazepines are exclusionary.

    13. Patients taking an excluded medication.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 The Ohio State University Columbus Ohio United States 43221

    Sponsors and Collaborators

    • Ohio State University

    Investigators

    • Principal Investigator: Maria Kataki, MD, Ohio State University

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Maria Kataki, MD, PhD, Associate Professor of Clinical Neurology, Ohio State University
    ClinicalTrials.gov Identifier:
    NCT04901494
    Other Study ID Numbers:
    • 2020H0375
    First Posted:
    May 25, 2021
    Last Update Posted:
    Sep 9, 2021
    Last Verified:
    Sep 1, 2021
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Maria Kataki, MD, PhD, Associate Professor of Clinical Neurology, Ohio State University
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Sep 9, 2021