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Augmented T-cell mitochondrial reactive oxygen species in adults with major depressive disorder.
Grotle, Ann-Katrin; Darling, Ashley M; Saunders, Erika F; Fadel, Paul J; Trott, Daniel W; Greaney, Jody L.
  • Grotle AK; Department of Kinesiology, University of Texas at Arlington, Arlington, Texas.
  • Darling AM; Department of Kinesiology, University of Texas at Arlington, Arlington, Texas.
  • Saunders EF; Department of Psychiatry and Behavioral Health, Penn State College of Medicine, and Penn State Health Milton S. Hershey Medical Center, Hershey, Pennsylvania.
  • Fadel PJ; Department of Kinesiology, University of Texas at Arlington, Arlington, Texas.
  • Trott DW; Department of Kinesiology, University of Texas at Arlington, Arlington, Texas.
  • Greaney JL; Department of Kinesiology, University of Texas at Arlington, Arlington, Texas.
Am J Physiol Heart Circ Physiol ; 322(4): H568-H574, 2022 04 01.
Article in English | MEDLINE | ID: covidwho-1706188
ABSTRACT
The prevalence of major depressive disorder (MDD) is highest in young adulthood, an effect that has been magnified by the COVID-19 pandemic. Importantly, individuals with MDD are at a greater risk of developing cardiovascular disease (CVD). Accumulating evidence supports immune system dysregulation as a major contributor to the elevated CVD risk in older adults with MDD; however, whether this is present in young adults with MDD without comorbid disease remains unclear. Interestingly, recent data suggest augmented T-cell mitochondrial reactive oxygen species (T-cell mitoROS) as a potent driver of immune dysregulation in animal models of psychiatric disease. With this background in mind, we tested the hypothesis that young adults with MDD would have augmented T-cell mitoROS and circulating proinflammatory cytokines compared with healthy young adults without MDD (HA). Whole blood was drawn from 14 young adults with MDD (age 23 ± 2 yr) and 11 HA (age 22 ± 1 yr). T-cell mitoROS (MitoSOX red; total CD3+, T-helper CD4+, T cytotoxic CD8+) and serum cytokines were assessed by flow cytometry. Total T-cell mitoROS was significantly greater in adults with MDD compared with HA [median 14,089 arbitrary units (AU); median 1,362 AU, P = 0.01]. Likewise, both T-helper and T-cytotoxic cell mitoROS were significantly greater in adults with MDD compared with HA (both P < 0.05). There were no differences in circulating cytokines between groups (all cytokines P > 0.05). Collectively, these findings suggest that elevated T-cell mitoROS may represent an early marker of immune system dysregulation in young, otherwise healthy, adults with MDD.NEW & NOTEWORTHY To our knowledge, we provide the first evidence of augmented T-cell mitochondrial reactive oxygen species (T-cell mitoROS) in young, otherwise healthy adults with MDD. Although the elevated T-cell mitoROS did not correspond to a proinflammatory profile, these findings suggest that elevated T-cell mitoROS may be an early marker of immune system dysregulation in young adults with MDD.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: T-Lymphocytes / Reactive Oxygen Species / Depressive Disorder, Major / Mitochondria Type of study: Experimental Studies / Observational study / Prognostic study / Qualitative research / Randomized controlled trials Limits: Adult / Female / Humans / Male / Young adult Language: English Journal: Am J Physiol Heart Circ Physiol Journal subject: Cardiology / Physiology Year: 2022 Document Type: Article

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Full text: Available Collection: International databases Database: MEDLINE Main subject: T-Lymphocytes / Reactive Oxygen Species / Depressive Disorder, Major / Mitochondria Type of study: Experimental Studies / Observational study / Prognostic study / Qualitative research / Randomized controlled trials Limits: Adult / Female / Humans / Male / Young adult Language: English Journal: Am J Physiol Heart Circ Physiol Journal subject: Cardiology / Physiology Year: 2022 Document Type: Article