大うつのRBDと嗅覚障害 | フレイルも認知症も減らない日本

フレイルも認知症も減らない日本

Nobody is in possession of the ultimate truth.

ウイルスと戦争の世紀で人生を終えることになるとは・・・まさに第三次世界大戦前夜の状況ですからね しかも本日は日本の金融市場はトリプル安

RBDを切り口にした
アプローチは見事。

機能的疾患から
器質的疾患への変容は
以前も取り上げましたが、
機能的疾患の代表である
大うつが、
RBDを併発して来ると、
器質的疾患である
αシヌクレイノパチーの
初期段階の可能性ありと。

嗅覚機能障害も
この仮説を
支持すると思います。



Reduced 
striatal 
dopamine 
transmission
in 
REM sleep 
behavior disorder 
comorbid with 
depression.

Authors

Wing YK1, 
Lam SP2, 
Zhang J2, 
Leung E2, 
Ho CL2, 
Chen S2, 
Cheung MK2, 
Li SX2, 
Chan JW2, 
Mok V2, 
Tsoh J2, 
Chan A2, 
Ho CK2.

Author information

1From the Department 
of Psychiatry
and 
the Department 
of Medicine 
and Therapeutics, 
Faculty of Medicine, 
The Chinese University 
of Hong Kong, 
Shatin, Hong Kong SAR; 
and Nuclear Medicine & PET, 
Hong Kong 
Sanatorium & Hospital. 

2From the Department 
of Psychiatry
and 
the Department 
of Medicine 
and Therapeutics, 
Faculty of Medicine, 
The Chinese University 
of Hong Kong, 
Shatin, Hong Kong SAR; 
and Nuclear Medicine & PET, 
Hong Kong 
Sanatorium & Hospital.

Journal

Neurology. 2015 Jan 7. 
pii: 10.1212/
WNL.0000000000001215. 


Abstract

OBJECTIVE: 

To investigate 
dopamine transmission 
in patients with 
comorbid REM sleep 
behavior disorder 
(RBD) and 
major 
depressive disorder
 (MDD).

METHODS: 

This is a case-control study 
including 
11 medicated patients
with comorbid RBD and MDD
 (mean age 47.5 ± 8.2), 
8 medicated patients 
with MDD only 
(mean age 47.9 ± 8.4), 
and 
10 healthy participants
 (mean age 46.5 ± 10.6 years). 

They underwent 
clinical assessment, 
video-polysomnography, 
olfactory tests, 
and neuroimaging studies
 ((18)F-DOPA, (11)C-raclopride, 
and 
(18)F-FDG PET neuroimaging).

RESULTS: 

Compared with 
the 2 control groups, 
patients 
with comorbid RBD and MDD 
had significantly 
lower (18)F-DOPA uptake 
at 60 minutes 
in the putamen and caudate 
after controlling for age 
and sex effect (p < 0.05). 

There were 
no significant differences 
for the (11)C-raclopride 
and (18)F-FDG-PET. 

The (18)F-DOPA uptake 
in putamens 
had significant 
inverse correlation with 
severity of RBD symptoms
 (p < 0.01) 
and 
REM-related 
tonic muscle activity
 (p < 0.01). 

The comorbid 
RBD and MDD group 
had more impairment 
in olfactory function.

CONCLUSION:

Patients 
with comorbid RBD and MDD 
had presynaptic 
dopamine dysfunction 
and 
impaired olfactory function. 

There is a distinct possibility 
that the development 
of RBD symptoms 
among patients with MDD 
may represent 
an early phase 
of α-synucleinopathy 
neurodegeneration 
instead of a 
merely 
antidepressant
-induced condition.