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K. Aydin, B. Tatli, M. Ozkan, K. Ciftci, Z. Unal, S. Sani, M. Ozmen, M. Caliskan, N. Aydinli, and S. Guven
Quantification of neurometabolites in subacute sclerosing panencephalitis by 1H-MRS
Neurology 2006; 67: 911-913
[Abstract][Full text][PDF]
The study of Aydin et al [1] adds to current data on the pathogenesis of subacute sclerosing panencephalitis (SSPE) and supports
the role of neuronal loss in the progression of neurological dysfunction.
The authors also observed increasing myoinositol (mI) until stage 3 of the
disease, which they related to astrogliosis. However, patients progressing
to stage 4 had lower concentrations of mI.
Because a reduction in
astrogliosis is unexpected in late stages of SSPE, I think this metabolite
might have been affected by inosiplex treatment as previously reported by Kato et al. [2] All patients in the study were under inosiplex treatment, but
compliance frequently diminishes when patients progress to more advanced
stages of the disease despite treatment. The role of medication should be
considered in interpreting MRS results.
References
1.Aydin K, Tatli B, Ozkan M, et al. Quantification of neurometabolites in
subacute sclerosing panencephalitis by 1H-MRS.Neurology 2006;67:911-913.
2.Kato Z, Asano T, Kondo N. Inosiplex Affects the Spectra of Proton
Magnetic Resonance Spectroscopy in Subacute Sclerosing Panencephalitis.
Journal of Child Neurology 2006;21:177-178.
Disclosure: The author reports no conflicts of interest.
Reply from the Authors
7 November 2006
Kubilay Aydin, Istanbul University, Istanbul Medical School, Department of Neuroradiology Adnan Saygun Cad. M. Salihrustu bey sok. Ulus Konaklari, No: 8/12, Ulus, Istanbul , Turkey
We appreciate Dr. Anlar’s comments about our recent article regarding MR
spectroscopy findings in patient with subacute sclerosing panencephalitis
(SSPE). We investigated the correlations between neurometabolite
concentrations and duration of disease and clinical status of patients
with SSPE. [1] In our study, the mean mI concentration of in the patients
with stage 4 disease was lower than that of stage 3 patients.
Dr. Anlar
speculates that the regression of mI increase in stage 4 patient might
have been caused by the effect of inosiplex. [2]. However, there was no change
in the treatment protocols or in inosiplex dosage which would support
such a hypothesis. Also, an increase in N-acetyl aspartate (NAA)
concentration accompanying the decrease in mI concentration would be
expected if the decrease in mI concentration in stage 4 patients was due
to theropeutic effect of inosiplex alone.
In our study, the NAA
concentrations continued to decrease in stage 3 patients who
progressed into stage 4. A case of SSPE
in which a regression of mI increase was observed when the patient
progressed into stage 4 disease has been reported. [3] There is no data to support Dr.
Anlar’s speculation. We hypothesize that tissue necrosis developing in
cerebral tissue of stage 4 patients may decrease mI concentration by a
diluting effect.
Our study was not a longitidunal
study focused on investigating the effect of inosiplex on proton
MR spectroscopy findings of SSPE patients. There is no current, adequate treatment for SSPE and inosiplex is one of the few drugs
which has been shown to be partially effective in the treatment of SSPE.
Due to ethical issues, we could not investigate potential
effects of inosiplex on neurometabolite concentrations. However, the
significant correlations of neurometabolite concentrations with clinical
status of patients which have been observed in our study makes MR
spectroscopy a potential clinical tool to follow up SSPE patients.
Reference
3. Michael N, Erfurth A, Ludemann P, Schuierer G, Moller HE. Serial
proton spectroscopy in a case of adult onset subacute sclerosing
panencephalitis. Psychiatry Res 2005; 139: 269-273.
Disclosure: The authors report no conflicts of interest.