Translational Psychiatry (Jun 2024)

A multi-site 99mTc-HMPAO SPECT study of cerebral blood flow in a community sample of patients with major depression

  • Bradley S. Peterson,
  • Jennifer Li,
  • Manuel Trujillo,
  • Siddhant Sawardekar,
  • David Balyozian,
  • Siddharth Bansal,
  • Bernice F. Sun,
  • Courtney Marcelino,
  • Anoop Nanda,
  • Tracy Xu,
  • Daniel Amen,
  • Ravi Bansal

DOI
https://doi.org/10.1038/s41398-024-02961-5
Journal volume & issue
Vol. 14, no. 1
pp. 1 – 10

Abstract

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Abstract Prior regional Cerebral Blood Flow (rCBF) studies in Major Depressive Disorder (MDD) have been limited by small, highly selective, non-representative samples that have yielded variable and poorly replicated findings. The aim of this study was to compare rCBF measures in a large, more representative community sample of adults with MDD and healthy control participants. This is a cross-sectional, retrospective multi-site cohort study in which clinical data from 338 patients 18–65 years of age with a primary diagnosis of MDD were retrieved from a central database for 8 privately owned, private-pay outpatient psychiatric centers across the United States. Two 99mTc-HMPAO SPECT brain scans, one at rest and one during performance of a continuous performance task, were acquired as a routine component of their initial clinical evaluation. In total, 103 healthy controls, 18–65 years old and recruited from the community were also assessed and scanned. Depressed patients had significantly higher rCBF in frontal, anterior cingulate, and association cortices, and in basal ganglia, thalamus, and cerebellum, after accounting for significantly higher overall CBF. Depression severity associated positively with rCBF in the basal ganglia, hippocampus, cerebellum, and posterior white matter. Elevated rCBF was especially prominent in women and older patients. Elevated rCBF likely represents pathogenic hypermetabolism in MDD, with its magnitude in direct proportion to depression severity. It is brain-wide, with disproportionate increases in cortical and subcortical attentional networks. Hypermetabolism may be a reasonable target for novel therapeutics in MDD.