TY - JOUR
T1 - Regional cerebral blood flow abnormalities in late-life depression
T2 - Relation to refractoriness and chronification
AU - Awata, Shuichi
AU - Ito, Hiroshi
AU - Konno, Michiko
AU - Ono, Shuichi
AU - Kawashima, Ryuta
AU - Fukuda, Hiroshi
AU - Sato, Mitsumoto
PY - 1998/2
Y1 - 1998/2
N2 - We examined patterns of regional cerebral blood flow (rCBF) abnormalities in 18 patients with major depressive disorder in late life using single photon emission computed tomography (SPECT) and (99m)Tc- hexamethylpropylenamine oxime ((99m)Tc-HMPAO). Compared with 13 age-matched controls, relative rCBF was significantly decreased bilaterally in the anterior cingulate gyrus, the prefrontal cortex, the temporal cortex, the parietal cortex, the hippocampus and the caudate nucleus. However, it was not correlated with the severity of depression or global cognitive dysfunction. In 10 patients with a prolonged depressive episode or prolonged residual symptoms (the refractory subgroup), robust and extensive decreases in rCBF were found compared with controls and the rCBF decreased significantly in the anterior cingulate gyrus and the prefrontal cortex compared with that in the non-refractory subgroup. In the non-refractory subgroup, rCBF decreased significantly in the caudate nucleus and tended to decrease in the anterior cingulate gyrus compared with controls. These findings indicate that dysfunction of the limbic system, the cerebral association cortex and the caudate nucleus may be implicated in late-life depression and that robust and extensive hypoperfusion, especially in the anterior cingulate and the prefrontal regions, may relate to refractoriness or chronification of depression.
AB - We examined patterns of regional cerebral blood flow (rCBF) abnormalities in 18 patients with major depressive disorder in late life using single photon emission computed tomography (SPECT) and (99m)Tc- hexamethylpropylenamine oxime ((99m)Tc-HMPAO). Compared with 13 age-matched controls, relative rCBF was significantly decreased bilaterally in the anterior cingulate gyrus, the prefrontal cortex, the temporal cortex, the parietal cortex, the hippocampus and the caudate nucleus. However, it was not correlated with the severity of depression or global cognitive dysfunction. In 10 patients with a prolonged depressive episode or prolonged residual symptoms (the refractory subgroup), robust and extensive decreases in rCBF were found compared with controls and the rCBF decreased significantly in the anterior cingulate gyrus and the prefrontal cortex compared with that in the non-refractory subgroup. In the non-refractory subgroup, rCBF decreased significantly in the caudate nucleus and tended to decrease in the anterior cingulate gyrus compared with controls. These findings indicate that dysfunction of the limbic system, the cerebral association cortex and the caudate nucleus may be implicated in late-life depression and that robust and extensive hypoperfusion, especially in the anterior cingulate and the prefrontal regions, may relate to refractoriness or chronification of depression.
KW - Anterior cingulate
KW - Chronification
KW - Late-life depression
KW - Prefrontal cortex
KW - Refractoriness
KW - Regional cerebral blood flow
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U2 - 10.1111/j.1440-1819.1998.tb00980.x
DO - 10.1111/j.1440-1819.1998.tb00980.x
M3 - Article
C2 - 9682941
AN - SCOPUS:0031977729
SN - 1323-1316
VL - 52
SP - 97
EP - 105
JO - Psychiatry and Clinical Neurosciences
JF - Psychiatry and Clinical Neurosciences
IS - 1
ER -