What this study is
Simplified from ClinicalTrials.govStudying immune system changes in blood to learn how they may be linked to depression in women ages 40 to 55 in perimenopause, the years before menopause. About half have depression and half do not; those with depression are tested again after about eight weeks.
Read the original summary from ClinicalTrials.gov
This project aims to identify immunobiological mechanisms underlying the development of depression during the perimenopause. During the perimenopause, the risk for recurrence of depression is increased 13-fold among women who previously had depression. Moreover, perimenopause overlaps with the age span exhibiting the highest suicide rate for women. The perimenopause can last for several years and starts when estrogen and progesterone levels begin to fluctuate, gradually declining. Sex hormones are powerful modulators of the immune response and the investigators therefore propose that changes in lymphocytes play a central role in depression during this time. Notably, our previous work has demonstrated deficient regulatory T-cell responses in women with post- partum depression and identified a specific pro-inflammatory profile that predicts depression during pregnancy. Importantly, our new pilot data derived from women with severe depression in the perimenopausal age span reveals alterations in tryptophan metabolites that control T- cell responses as well as in the methylation of genes involved in T-cell fate and chromatin remodeling. Taken together, these data support the hypothesis that the perimenopausal hormonal shifts induce a pro-inflammatory state, regulated by chromatin modifications in T-cells, that triggers depression in vulnerable women.
To test this hypothesis, the investigators will enroll 180 perimenopausal women aged 40-55, approximately half with depression and half without a diagnosis of depression. All participants will complete psychiatric assessments and provide blood samples to measure sex hormones, inflammation and immune cell changes. Women with depression will be reassessed approximately eight weeks later to identify blood markers that change as depressive symptoms improve.
This project seeks to improve understanding of the biological mechanisms of depression during perimenopause and aid the development of predictive biomarkers and more effective treatments.
Study details
- Sponsor
- Van Andel Research Institute
- Conditions
- Perimenopause · Major Depressive Episode (MDE)
- Enrolling
- 120 people
- Starts
- 2025-03-13
- Est. completion
- 2031-11-30
- Record
- View on ClinicalTrials.gov ↗
Who can join
Age 40 Years – 55 YearsSex FEMALEHealthy volunteers AcceptedYou may qualify if
- Biological women, age 40 to 55.
- Undergoing perimenopause according to STRAW criteria [1].
- All races and national origins can be included.
- English speaking (since all clinical rating scales to be used here have not been developed and validated for non-English speaking populations).
- Able to give informed consent.
- Able to comply with and complete study procedures.
- Willing and able to take part of the different steps in the study, including follow-up research visit after 8 weeks and blood draws.
You can't join if
- Pregnant, nursing or transgender women (due to their hormonal status being different than what is investigated in this project).
- Incarcerated individuals.
- Subjects with dementia or otherwise cognitively impaired subjects with difficulty understanding the study procedures.
- Patients with an active somatic disorder primarily involving the immune system (autoimmune diseases such as Crohn's disease, multiple sclerosis, or rheumatoid arthritis; or hematological diseases such as lymphoma or leukemia or HIV). Research staff will consult with the PIs in cases of uncertainty.
- Patients with untreated hormonal conditions affecting the reproductive system.
- Patients on chronic and systemic immunomodulatory treatment. Examples are patients with a liver or kidney transplant and medications used for disorders involving the immune system, as mentioned above. Examples of immunomodulatory treatments are cyclosporin, azathioprine, infliximab and chronic corticosteroid treatment.
- Women already taking hormonal substitution before the research visit (either for perimenopause or/and as contraceptive) or replacement will be excluded,
- Patients taking lithium, neuroleptic- or mood stabilizing medications (antidepressants, such as SSRIs and SNRIs, are allowed).
- Patients undergoing active treatment for any form of cancer (chemotherapy or immunomodulatory treatments).
Sign in and we'll check these against your records.Full criteria on ClinicalTrials.gov ↗
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Study locations (4)
3 openPine Rest Christian Mental Health
Grand Rapids, Michigan, United States
- Nagy Youssef, MD, PHD · Contact616-281-6363Nagy.Youssef@pinerest.org
- Janelle Kassien · Contactjanelle.kassien@pinerest.org
RecruitingWestern Michigan University Homer Stryker M.D. School of Medicine
Kalamazoo, Michigan, United States
- Eric Achytes, MD, MS · Contact269-337-4350Eric.Achtyes@WMed.edu
- Heather Mayle · Contactheather.mayle@wmed.edu
RecruitingWeill Cornell Medicine
New York, New York, United States
- Lauren M. Osborne, MD · Contact212-746-3154lmo2003@med.cornell.edu
- Nathaly Tavarez · Contactnat4012@med.cornell.edu
RecruitingVan Andel Institute
Grand Rapids, Michigan, United States
Active, not recruiting
Study team
Sponsor
Van Andel Research Institute
Study ID 24021
Principal investigator
Lena Cecilia Brundin, MD, PhD
Van Andel Research Institute
Principal investigator
Nagy Youssef, MD, PhD
Pine Rest Christian Mental Health
Principal investigator
Eric Achytes, MD, MS
Western Michigan University Homer Stryker M.D. School of Medicine
Principal investigator
Lauren M. Osborne, MD
Weill Medical College of Cornell University
Frequently asked questions
The sponsor hasn't published answers to common questions for this trial.