Medial temporal lobe volumes in late-life depression: effects of age and vascular risk factors.

Substantial work associates late-life depression with hippocampal pathology. However, there is less information about differences in hippocampal subfields and other connected temporal lobe regions and how these regions may be influenced by vascular factors. Individuals aged 60 years or older with an...

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Publicado en:Brain Imaging & Behavior Vol. 14; no. 1; pp. 19 - 30
Autores principales: Taylor, Warren D., Deng, Yi, Boyd, Brian D., Donahue, Manus J., Albert, Kimberly, McHugo, Maureen, Gandelman, Jason A, Landman, Bennett A.
Formato: Journal Article
Publicado: Springer Nature Feb2020
Acceso en línea:Ver este registro en EBSCOhost
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        atl: Medial temporal lobe volumes in late-life depression: effects of age and vascular risk factors.
      aug:
        au:
          Taylor, Warren D.
          Deng, Yi
          Boyd, Brian D.
          Donahue, Manus J.
          Albert, Kimberly
          McHugo, Maureen
          Gandelman, Jason A
          Landman, Bennett A.
        affil: The Department of Psychiatry and Behavioral Sciences, Vanderbilt University Medical Center, 1601 23rd Avenue South, 37212, Nashville, TN, USA
      sug:
        subj:
          Depression Physiopathology
          Temporal Lobe Physiopathology
          Cerebrovascular Circulation Physiology
          Depression Metabolism
          Hippocampus Pathology
          Atrophy Pathology
          Magnetic Resonance Imaging Methods
          Aged, 80 and Over
          Middle Age
          Cerebral Cortex Pathology
          Aged
          Male
          Risk Factors
          Temporal Lobe Metabolism
          Age Factors
          Prospective Studies
          Female
          Scales
          Aged, 80 & over
          Middle Aged: 45-64 years
          Aged: 65+ years
          Male
          Female
      ab: Substantial work associates late-life depression with hippocampal pathology. However, there is less information about differences in hippocampal subfields and other connected temporal lobe regions and how these regions may be influenced by vascular factors. Individuals aged 60 years or older with and without a DSM-IV diagnosis of Major Depressive Disorder completed clinical assessments and 3 T cranial MRI using a protocol allowing for automated measurement of medial temporal lobe subfield volumes. A subset also completed pseudo-continuous arterial spin labeling, allowing for the measurement of hippocampal cerebral blood flow. In 59 depressed and 21 never-depressed elders (mean age = 66.4 years, SD = 5.8y, range 60-86y), the depressed group did not exhibit statistically significant volumetric differences for the total hippocampus or hippocampal subfields but did exhibit significantly smaller volumes of the perirhinal cortex, specifically in the BA36 region. Additionally, age had a greater effect in the depressed group on volumes of the cornu ammonis, entorhinal cortex, and BA36 region. Finally, both clinical and radiological markers of vascular risk were associated with smaller BA36 volumes, while reduced hippocampal blood flow was associated with smaller hippocampal and cornu ammonis volumes. In conclusion, while we did not observe group differences in hippocampal regions, we observed group differences and an effect of vascular pathology on the BA36 region, part of the perirhinal cortex. This is a critical region exhibiting atrophy in prodromal Alzheimer's disease. Moreover, the observed greater effect of age in the depressed groups is concordant with past longitudinal studies reporting greater hippocampal atrophy in late-life depression.
      pubtype: Academic Journal
      doctype: Journal Article
      ougenre: Article
    language: English
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