Human dorsal root ganglion in vivo morphometry and perfusion in Fabry painful neuropathy

被引:43
作者
Godel, Tim [1 ]
Baeumer, Philipp [1 ,2 ]
Pham, Mirko [1 ,3 ]
Koehm, Anja [4 ]
Muschol, Nicole [4 ]
Kronlage, Moritz [1 ]
Kollmer, Jennifer [1 ]
Heiland, Sabine [1 ]
Bendszus, Martin [1 ]
Mautner, Victor-Felix [5 ]
机构
[1] Heidelberg Univ Hosp, Neurol Univ Clin, Dept Neuroradiol, Heidelberg, Germany
[2] German Canc Res Inst, Dept Radiol, Heidelberg, Germany
[3] Wurzburg Univ Hosp, Dept Neuroradiol, Wurzburg, Germany
[4] Univ Med Ctr Hamburg Eppendorf, Dept Pediat, Hamburg, Germany
[5] Univ Med Ctr Hamburg Eppendorf, Dept Neurol, Hamburg, Germany
关键词
SENSORY NEURONS; DISEASE; INVOLVEMENT; SYSTEM; PREVALENCE; MECHANISM; FEMALES;
D O I
10.1212/WNL.0000000000004396
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective: To evaluate functional and morphometric magnetic resonance neurography of the dorsal root ganglion and peripheral nerve segments in patients with Fabry painful neuropathy. Methods: In this prospective study, the lumbosacral dorsal root ganglia and proximal peripheral nerve segments of the lower extremity were examined in 11 male patients with Fabry disease by a standardized 3T magnetic resonance neurography protocol. Volumes of L3 to S2 dorsal root ganglia, perfusion parameters of L5-S1 dorsal root ganglia and the spinal nerve L5, and the cross-sectional area of the proximal sciatic nerve were compared to healthy controls. Results: Dorsal root ganglia of patients with Fabry disease were symmetrically enlarged by 78% (L3), 94% (L4), 122% (L5), 115% (S1), and 119% (S2) (p < 0.001). In addition, permeability of the blood-tissue interface was decreased by 53% (p < 0.001). This finding was most pronounced in the peripheral zone of the dorsal root ganglion containing the cell bodies of the primary sensory neurons (p < 0.001). Spinal nerve permeability showed no difference between patients with Fabry disease and controls (p = 0.7). The sciatic nerve of patients with Fabry disease at the thigh level showed an increase in cross-sectional area by 48% (p < 0.001). Conclusions: Patients with Fabry disease have severely enlarged dorsal root ganglia with dysfunctional perfusion. This may be due to glycolipid accumulation in the dorsal root ganglia mediating direct neurotoxic effects and decreased neuronal blood supply. These alterations were less pronounced in peripheral nerve segments. Thus, the dorsal root ganglion might play a key pathophysiologic role in the development of neuropathy and pain in Fabry disease.
引用
收藏
页码:1274 / 1282
页数:9
相关论文
共 43 条
[1]   Elevated globotriaosylsphingosine is a hallmark of Fabry disease [J].
Aerts, Johannes M. ;
Groener, Johanna E. ;
Kuiper, Sijmen ;
Donker-Koopman, Wilma E. ;
Strijland, Anneke ;
Ottenhoff, Roelof ;
van Roomen, Cindy ;
Mirzaian, Mina ;
Wijburg, Frits A. ;
Linthorst, Gabor E. ;
Vedder, Anouk C. ;
Rombach, Saskia M. ;
Cox-Brinkman, Josanne ;
Somerharju, Pentti ;
Boot, Rolf G. ;
Hollak, Carla E. ;
Brady, Roscoe O. ;
Poorthuis, Ben J. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2008, 105 (08) :2812-2817
[2]   Enhanced endothelium-dependent vasodilation in Fabry disease [J].
Altarescu, G ;
Moore, DF ;
Pursley, R ;
Campia, U ;
Goldstein, S ;
Bryant, M ;
Panza, JA ;
Schiffmann, R .
STROKE, 2001, 32 (07) :1559-1562
[3]   FENESTRATED BLOOD CAPILLARIES IN RAT CRANIO-SPINAL SENSORY GANGLIA [J].
ANZIL, AP ;
BLINZINGER, K ;
HERRLINGER, H .
CELL AND TISSUE RESEARCH, 1976, 167 (04) :563-567
[4]   Molecular mechanisms of calcium-dependent neurodegeneration in excitotoxicity [J].
Arundine, M ;
Tymianski, M .
CELL CALCIUM, 2003, 34 (4-5) :325-337
[5]   The Fabry disease-associated lipid Lyso-Gb3 enhances voltage-gated calcium currents in sensory neurons and causes pain [J].
Choi, L. ;
Vernon, J. ;
Kopach, O. ;
Mitlett, M. S. ;
Mills, K. ;
Clayton, P. T. ;
Meert, T. ;
Wood, J. N. .
NEUROSCIENCE LETTERS, 2015, 594 :163-168
[6]   Fabry disease peripheral blood immune cells release inflammatory cytokines: Role of globotriaosylceramide [J].
De Francesco, Pablo N. ;
Mucci, Juan M. ;
Ceci, Romina ;
Fossati, Carlos A. ;
Rozenfeld, Paula A. .
MOLECULAR GENETICS AND METABOLISM, 2013, 109 (01) :93-99
[7]  
DeGraba T, 2000, ANN NEUROL, V47, P229, DOI 10.1002/1531-8249(200002)47:2<229::AID-ANA13>3.0.CO
[8]  
2-T
[9]  
Desnick RJ, 2001, CONTRIB NEPHROL, V136, P174
[10]  
Devor M, 1999, PAIN, pS27, DOI 10.1016/S0304-3959(99)00135-9