Literature DB >> 9520004

Proton spectroscopy in myotonic dystrophy: correlations with CTG repeats.

L Chang1, T Ernst, D Osborn, W Seltzer, M Leonido-Yee, R E Poland.   

Abstract

OBJECTIVES: To seek cerebral metabolite abnormalities in patients with myotonic dystrophy and to determine whether the degree of cerebral abnormalities (measured by proton magnetic resonance spectroscopy) correlates with severity of the genetic defect (measured by trinucleotide repeats).
DESIGN: Fourteen patients with myotonic dystrophy were compared with 24 healthy control subjects.
SETTING: A university-affiliated medical center.
RESULTS: Compared with healthy subjects, patients with myotonic dystrophy had elevated levels of myoinositol (+19% in the occipital region and +12.9% in the temporoparietal region), total creatine (+7.6% and +6.8%), and choline-containing compounds (+21% and +7.7%). Furthermore, the creatine and myoinositol peak areas correlated with the number of trinucleotide cytosine-thymine-guanine(n) (CTG)n repeats from leukocytes, especially in the temporoparietal brain region (r=0.76; P=.004).
CONCLUSIONS: Neurochemical alterations observed with proton magnetic resonance spectroscopy are proportional to the cytosine-thymine-guanine repeat size. Increases in myoinositol and creatine concentrations may be caused by increased glial content, while elevated levels of choline-containing compounds are most likely caused by increased glial content and cell membrane abnormalities. Proton magnetic resonance spectroscopy is a powerful noninvasive tool to study brain biochemistry, which may reflect the extent of neuropathological involvement in patients with myotonic dystrophy.

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Year:  1998        PMID: 9520004     DOI: 10.1001/archneur.55.3.305

Source DB:  PubMed          Journal:  Arch Neurol        ISSN: 0003-9942


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