Correlative MR imaging and 31P-MR spectroscopy study in sarcoglycan deficient limb girdle muscular dystrophy

被引:41
作者
Lodi, R [1 ]
Muntoni, F
Taylor, J
Kumar, S
Sewry, CA
Blamire, A
Styles, P
Taylor, DJ
机构
[1] Oxford Radcliffe Hosp, MRC Biochem & Clin, Magnet Resonance Unit, Oxford OX3 9DU, England
[2] Hammersmith Hosp, Neuromuscular Unit, Dept Paediat & Neonatal Med, London, England
关键词
muscular dystrophy; sarcoglycan; in vivo phosphorous magnetic resonance spectroscopy; magnetic resonance imaging;
D O I
10.1016/S0960-8966(97)00108-9
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
We combined magnetic resonance (MR) imaging and phosphorus magnetic resonance spectroscopy (P-31-MRS) to study skeletal muscle in seven patients with limb girdle muscular dystrophy (LGMD) with a variable deficiency of the alpha-, beta-, and gamma-sarcoglycan but normal dystrophin expression on muscle biopsy. T1- and T2-weighted spin-echo axial leg images showed the highest degree of fat replacement in soleus, tibialis anterior and peroneal muscles while gastrocnemius and tibialis posterior were less affected. In LGMD patients as a group, calf muscle phosphorylated compound content did not differ from controls, but the cytosolic pH was increased (P = 0.02). The degree of calf muscle fat replacement correlated inversely with cytosolic pH (r = 0.74) and directly with PCr/ATP (r = 0.74). Muscle oxidative metabolism was normal in LGMD patients. Our findings show that primary deficits of sarcoglycan complex lead to specific morphological and metabolic patterns of skeletal muscle involvement. (C) 1997 Elsevier Science B.V.
引用
收藏
页码:505 / 511
页数:7
相关论文
共 33 条
[1]
METABOLIC RECOVERY AFTER EXERCISE AND THE ASSESSMENT OF MITOCHONDRIAL-FUNCTION INVIVO IN HUMAN SKELETAL-MUSCLE BY MEANS OF P-31 NMR [J].
ARNOLD, DL ;
MATTHEWS, PM ;
RADDA, GK .
MAGNETIC RESONANCE IN MEDICINE, 1984, 1 (03) :307-315
[2]
INVESTIGATION OF HUMAN MITOCHONDRIAL MYOPATHIES BY PHOSPHORUS MAGNETIC-RESONANCE SPECTROSCOPY [J].
ARNOLD, DL ;
TAYLOR, DJ ;
RADDA, GK .
ANNALS OF NEUROLOGY, 1985, 18 (02) :189-196
[3]
HUMAN LEG NEUROMUSCULAR DISEASES - P-31 MR SPECTROSCOPY [J].
BARANY, M ;
SIEGEL, IM ;
VENKATASUBRAMANIAN, PN ;
MOK, E ;
WILBUR, AC .
RADIOLOGY, 1989, 172 (02) :503-508
[4]
P-31-NMR SPECTROSCOPY OF SKELETAL-MUSCLE IN BECKER DYSTROPHY AND DMD BMD CARRIERS - ALTERED RATE OF PHOSPHATE-TRANSPORT [J].
BARBIROLI, B ;
FUNICELLO, R ;
IOTTI, S ;
MONTAGNA, P ;
FERLINI, A ;
ZANIOL, P .
JOURNAL OF THE NEUROLOGICAL SCIENCES, 1992, 109 (02) :188-195
[5]
SKELETAL-MUSCLE BIOENERGETICS IN THE CHRONIC FATIGUE SYNDROME [J].
BARNES, PRJ ;
TAYLOR, DJ ;
KEMP, GJ ;
RADDA, GK .
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 1993, 56 (06) :679-683
[6]
BETA-SARCOGLYCAN (A3B) MUTATIONS CAUSE AUTOSOMAL RECESSIVE MUSCULAR-DYSTROPHY WITH LOSS OF THE SARCOGLYCAN COMPLEX [J].
BONNEMANN, CG ;
MODI, R ;
NOGUCHI, S ;
MIZUNO, Y ;
YOSHIDA, M ;
GUSSONI, E ;
MCNALLY, EM ;
DUGGAN, DJ ;
ANGELINI, C ;
HOFFMAN, EP ;
OZAWA, E ;
KUNKEL, LM .
NATURE GENETICS, 1995, 11 (03) :266-273
[8]
3 MUSCULAR-DYSTROPHIES - LOSS OF CYTOSKELETON EXTRACELLULAR-MATRIX LINKAGE [J].
CAMPBELL, KP .
CELL, 1995, 80 (05) :675-679
[9]
DUBOWITZ V, 1989, MUSCLE BIOPSY PRACTI
[10]
DUNN J, 1991, BIOCHIM BIOPHYS ACTA, P115