Characteristics of Patients With Late-Onset Pompe Disease in France

被引:5
|
作者
Lefeuvre, Claire [1 ,2 ]
De Antonio, Marie [3 ]
Bouhour, Francoise [4 ]
Tard, Celine [2 ,5 ]
Salort-Campana, Emmanuelle [6 ,7 ]
Lagrange, Emmeline [8 ]
Behin, Anthony [2 ,9 ]
Sole, Guilhem [10 ]
Noury, Jean-Baptiste [11 ]
Sacconi, Sabrina [12 ]
Magot, Armelle [13 ]
Nadaj-Pakleza, Aleksandra [2 ,14 ]
Lacour, Arnaud [15 ]
Beltran, Stephane [16 ]
Spinazzi, Marco [17 ]
Cintas, Pascal [18 ]
Renard, Dimitri [19 ]
Michaud, Maud [2 ,20 ]
Bedat-Millet, Anne-Laure [21 ]
Prigent, Helene [2 ,22 ,23 ]
Taouagh, Nadjib [1 ,2 ]
Arrassi, Azzeddine [2 ,9 ]
Hamroun, Dalil [24 ]
Attarian, Shahram [6 ,7 ]
Laforet, Pascal [1 ,2 ,23 ]
Pompe Study Grp
机构
[1] Raymond Poincare Univ Hosp, AP HP, Neurol Dept, Garches, France
[2] FHU PHENIX, Nord Est Ile De France Neuromuscular Reference Ctr, Garches, France
[3] Clermont Ferrand Univ Hosp, Biostat Unit DRCI, Clermont Ferrand, France
[4] Hosp Civils Lyon, Serv Electroneuromyog & Pathol Neuromusculaires, Lyon, France
[5] Univ Lille, Lille Univ Hosp Ctr, Inserm, U1172,Lille Neurosci & Cognit, Lille, France
[6] Hop Timone Adultes, AP HM, Ctr Reference Malad Neuromusculaires, Marseille, France
[7] FILNEMUS, PACA Reunion Rhone Alpes Reference Ctr Neuromuscul, Marseille, France
[8] Grenoble Univ Hosp, Dept Neurol, Grenoble, France
[9] GH Pitie Salpetriere, AP HP, Inst Myol, Serv Neuromyol, Paris, France
[10] Univ Bordeaux, Bordeaux Univ Hosp Pellegrin, Neuromuscular Reference Ctr, Bordeaux, France
[11] CHRU Cavale Blanche, Neuromuscular Ctr, Neurol Dept, Brest, France
[12] Univ Cote Azur, CHU Nice, Peripheral Nervous Syst & Muscle Dept, Nice, France
[13] CHU Hotel Dieu, Ctr Reference Malad Neuromusculaires AOC, Nantes, France
[14] Univ Hosp, Dept Neurol, Strasbourg, France
[15] CHU St Etienne, Hop Nord, Ctr Reference Malad Neuromusculaires Rares Rhone A, St Etienne, France
[16] Francois Rabelais Univ, ALS Ctr, Tours, Centre Val De L, France
[17] Univ Hosp, Neuromuscular Reference Ctr, Dept Neurol, Angers, France
[18] CHU Toulouse, Hop Purpan, Dept Neurol, Toulouse, France
[19] Univ Montpellier, CHU Nimes, Dept Neurol, Nimes, France
[20] Nancy Univ Hosp, Dept Neurol, Nancy, France
[21] Rouen Univ Hosp, Neuromuscular Reference Ctr, Rouen, France
[22] GH Paris Ile France Ouest, AP HP, Serv Physiol & Explorat Fonct, Site Raymond Poincare, Garches, France
[23] Univ Versailles St Quentin Yvelines, Paris Saclay, INSERM, U1179, Yvelines, France
[24] CHU Montpellier, Hop Arnaud De Villeneuve, Montpellier, France
关键词
ACID MALTASE DEFICIENCY; THERAPY;
D O I
10.1212/WNL.0000000000207547
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background and ObjectivesThe French Pompe disease registry was created in 2004 for study of the natural course of the disease in patients. It rapidly became a major tool for assessing the long-term efficacy of enzyme replacement therapy (ERT) after the market release of alglucosidase-alfa.MethodsApproximately 10 years after publication of the baseline characteristics of the 126 initial patients of the French Late-Onset Pompe Disease registry, we provide here an update of the clinical and biological features of patients included in this registry.ResultsWe describe 210 patients followed at 31 hospital-based French neuromuscular or metabolic centers. The median age at inclusion was 48.67 & PLUSMN; 14.91 years. The first symptom was progressive lower limb muscle weakness, either isolated (50%) or associated with respiratory symptoms (18%), at a median age of 38 & PLUSMN; 14.9 years. At inclusion, 64% of the patients were able to walk independently and 14% needed a wheelchair. Positive associations were found between motor function measure, manual motor test, and 6-minute walk test (6MWT) results, and these parameters were inversely associated with the time taken to sit up from a lying position at inclusion. Seventy-two patients had been followed for at least 10 years in the registry. Thirty-three patients remained untreated a median of 12 years after symptom onset. The standard ERT dose was administered for 177 patients.DiscussionThis update confirms previous findings for the adult population included in the French Pompe disease registry, but with a lower clinical severity at inclusion, suggesting that this rare disease is now diagnosed earlier; thanks to greater awareness among physicians. The 6MWT remains an important method for assessing motor performance and walking ability. The French Pompe disease registry provides an exhaustive, nationwide overview of Pompe disease and can be used to assess individual and global responses to future treatments.
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收藏
页码:E966 / E977
页数:12
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