TY - JOUR
T1 - Regional metabolic rate of glucose (CMRglu) evaluation and clinical assessment in idiopathic normal-pressure hydrocephalus (iNPH) patients before and after ventricular shunt placement. A prospective analysis
AU - Calcagni, Maria Lucia
AU - Taralli, Silvia
AU - Mangiola, Annunziato
AU - Indovina, Luca
AU - Lavalle, Maria Dea
AU - De Bonis, Pasquale
AU - Anile, Carmelo
AU - Giordano, Alessandro
PY - 2013
Y1 - 2013
N2 - Purpose: We prospectively evaluated the regional cerebral metabolic rate of
glucose (CMRglu) before and after ventricular shunt placement in idiopathic
normal-pressure hydrocephalus (iNPH) patients, to investigate whether some
brain regions are more involved than others; we also correlated the individual
variations of CMRglu with the clinical scale score assessment after shunting.
Methods: Twenty iNPH patients (12 men; mean age, 73 T 9 years) underwent
clinical scale score assessment and 18F-FDG PET-CT before and 1 week after
shunting.
Results: Before shunting, CMRglu values were similar in right and left brain
regions, as well as after shunting. After shunting, 17 of 20 iNPH patients were
clinically improved; all scale scores decreased, and CMRglu significantly increased
in all regions (P G 10j7). In 3 of 20 iNPH patients, the symptoms
persisted, the scale scores did not change, and CMRglu increased only in
3 regions: left frontal, left putamen, and right thalamus. Before shunting, no
difference in global CMRglu between clinically improved (n = 17) and not
improved (n = 3) iNPH patients was found. After shunting, a significant
(P = 0.01) correlation between individual variations of CMRglu and clinical
assessment was found.
Conclusions: These findings confirm that iNPH is a disease involving all
cerebral regions almost in the same way, and shunt procedure has a similar
effect on regional cerebral metabolism almost in the same way. Individual
variations of CMRglu are more important than absolute values and correlate
with clinical status after shunting. Clinical improvement depends not only on
the capability to restore the cerebrospinal fluid dynamic, but also on the ability
of cerebral parenchyma to recover the metabolic function.
AB - Purpose: We prospectively evaluated the regional cerebral metabolic rate of
glucose (CMRglu) before and after ventricular shunt placement in idiopathic
normal-pressure hydrocephalus (iNPH) patients, to investigate whether some
brain regions are more involved than others; we also correlated the individual
variations of CMRglu with the clinical scale score assessment after shunting.
Methods: Twenty iNPH patients (12 men; mean age, 73 T 9 years) underwent
clinical scale score assessment and 18F-FDG PET-CT before and 1 week after
shunting.
Results: Before shunting, CMRglu values were similar in right and left brain
regions, as well as after shunting. After shunting, 17 of 20 iNPH patients were
clinically improved; all scale scores decreased, and CMRglu significantly increased
in all regions (P G 10j7). In 3 of 20 iNPH patients, the symptoms
persisted, the scale scores did not change, and CMRglu increased only in
3 regions: left frontal, left putamen, and right thalamus. Before shunting, no
difference in global CMRglu between clinically improved (n = 17) and not
improved (n = 3) iNPH patients was found. After shunting, a significant
(P = 0.01) correlation between individual variations of CMRglu and clinical
assessment was found.
Conclusions: These findings confirm that iNPH is a disease involving all
cerebral regions almost in the same way, and shunt procedure has a similar
effect on regional cerebral metabolism almost in the same way. Individual
variations of CMRglu are more important than absolute values and correlate
with clinical status after shunting. Clinical improvement depends not only on
the capability to restore the cerebrospinal fluid dynamic, but also on the ability
of cerebral parenchyma to recover the metabolic function.
KW - IDROCEPHALUS
KW - IDROCEPHALUS
UR - http://hdl.handle.net/10807/42026
M3 - Article
SN - 0363-9762
SP - N/A-N/A
JO - Clinical Nuclear Medicine
JF - Clinical Nuclear Medicine
ER -