Dysarthria and dysphagia in patients with mitochondrial diseases

被引:1
|
作者
Kuin, R. E. M. [1 ]
Groothuis, J. T. [2 ,4 ]
Buit, P. [3 ,4 ]
Janssen, M. C. H. [3 ,4 ]
Knuijt, S. [2 ,4 ,5 ]
机构
[1] Radboud Univ Nijmegen, MA Speech Language Pathol, Nijmegen, Netherlands
[2] Radboud Univ Nijmegen, Med Ctr, Dept Rehabil, Donders Inst Brain Cognit & Behav, Nijmegen, Netherlands
[3] Radboud Univ Nijmegen, Med Ctr, Dept Internal Med, Nijmegen, Netherlands
[4] Radboudumc, Radboud Ctr Mitochondrial Med RCMM, Nijmegen, Netherlands
[5] Radboud Univ Nijmegen, Med Ctr, Dept Rehabil, 907 POB 9101, NL-6500 HB Nijmegen, Netherlands
关键词
Mitochondrial diseases; Dysarthria; Dysphagia; Speech and language therapy; Adults; SCALE; RELIABILITY; PREVALENCE;
D O I
10.1016/j.ymgme.2024.108510
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Information about dysarthria and dysphagia in mitochondrial diseases (MD) is scarce. However, this knowledge is needed to identify speech and swallowing problems early, to monitor the disease course, and to develop and offer optimal treatment and support. This study therefore aims to examine the prevalence and severity of dysarthria and dysphagia in patients with MD and its relation to clinical phenotype and disease severity. Secondary aim is to determine clinically relevant outcome measures for natural history studies and clinical trials. Methods: This retrospective cross-sectional medical record study includes adults (age >= 18 years) diagnosed with genetically confirmed MD who participated in a multidisciplinary admission within the Radboud center for mitochondrial medicine between January 2015 and April 2023. Dysarthria and dysphagia were examined by administering the Radboud dysarthria assessment, swallowing speed, dysphagia limit, test of mastication and swallowing solids (TOMASS), and 6 -min mastication test (6MMT). The disease severity was assessed using the Newcastle mitochondrial disease scale for adults (NMDAS). Results: The study included 224 patients with MD with a median age of 42 years of whom 37.5% were male. The pooled prevalence of dysarthria was 33.8% and of dysphagia 35%. Patients with MD showed a negative deviation from the norm on swallowing speed, TOMASS (total time) and the 6MMT. Furthermore, a significant moderate relation was found between the presence of dysarthria and the clinical phenotypes. There was a statistically significant difference in total time on the TOMASS between the clinical phenotypes. Finally, disease severity showed a significant moderate relation with the severity of dysarthria and a significant weak relation with the severity of dysphagia. Conclusion: Dysarthria and dysphagia occur in about one-third of patients with MD. It is important for treating physicians to pay attention to this subject because of the influence of both disorders on social participation and wellbeing. Referral to a speech and language therapist should therefore be considered, especially in patients with a more severe clinical phenotype. The swallowing speed, TOMASS and 6MMT are the most clinically relevant tests to administer.
引用
收藏
页数:8
相关论文
共 50 条
  • [41] PHARMACOLOGICAL ASPECTS AND NEUROLOGICAL SPEECH THERAPY: TARGET OF DYSPHONY, DYSARTHRIA AND DYSPHAGIA
    Megna, M.
    Cortese, R.
    Dellomonaco, A.
    Bellomo, R. G.
    Salonnna, I.
    Cristella, G.
    Ranieri, M.
    INTERNATIONAL JOURNAL OF IMMUNOPATHOLOGY AND PHARMACOLOGY, 2012, 25 : 29 - 33
  • [42] Ventrally exophytic pontine mass in a patient with dysarthria, dysphagia and diplopia: Answer
    Ovenden, Christopher
    O'Donohoe, Thomas
    Santoreneos, Stephen
    JOURNAL OF CLINICAL NEUROSCIENCE, 2021, 86 : 310 - 311
  • [43] PALATO-PHARYNGO-LARYNGEAL MYOCLONUS - AN UNUSUAL CAUSE OF DYSPHAGIA AND DYSARTHRIA
    DRYSDALE, AJ
    ANSELL, J
    ADELEY, J
    JOURNAL OF LARYNGOLOGY AND OTOLOGY, 1993, 107 (08): : 746 - 747
  • [44] Relapsing remitting multiples sclerosis (RR-MS) IN Chile. Evolution of dysphagia and dysarthria in 84 patients
    Araya, S. Casandra
    Flores, C. Jazmin
    Lara, G. Fabiola
    Quezada, J. Gaston
    Nogales, G. Jorge
    Aracena, C. Rodrigo
    Agurto, M. Paula
    Eloiza, C. Claudio
    Acevedo, G. Lorena
    Cepeda, Z. Sergio
    Diaz, Z. Vannia
    Martinez, E. Sefora
    Labbe, R. Silvia
    MULTIPLE SCLEROSIS JOURNAL, 2012, 18 (12) : 1862 - 1862
  • [45] A significant association between dysphagia and malnutrition in patients with acute diseases
    Saito, T.
    Hayashi, K.
    Nakazawa, H.
    Yagihashi, F.
    Oikawa, L.
    Ota, T.
    JOURNAL OF THE NEUROLOGICAL SCIENCES, 2017, 381 : 1072 - 1072
  • [46] Dysarthria in Patients with Schizophrenia
    Fusick, Adam J.
    Wagner, Sienna S.
    Kamath, Vandan D.
    Stewart, Jonathan T.
    PSYCHIATRIC ANNALS, 2020, 50 (01) : 33 - 37
  • [47] Protein Nitration in Patients with Mitochondrial Diseases
    Livramento, Jomenica B.
    Rodrigues, Gabriela S.
    Faber, Jean
    de Souza Filho, Luis A.
    Moura, Felipo V.
    Barros, Camila D. S.
    Pinto, Wladimir B. V. R.
    Schmidt, Beny
    Oliveira, Acary S. B.
    Kiyomoto, Beatriz H.
    Tengan, Celia H.
    ANTIOXIDANTS, 2025, 14 (02)
  • [48] The brain is hypothermic in patients with mitochondrial diseases
    Rango, Mario
    Arighi, Andrea
    Bonifati, Cristiana
    Del Bo, Roberto
    Comi, Giacomo
    Bresolin, Nereo
    JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 2014, 34 (05): : 915 - 920
  • [49] Social provisions in patients with mitochondrial diseases
    Haque, Sameen
    Crawley, Karen
    Schofield, Deborah
    Shrestha, Rupendra
    Davis, Ryan
    Sue, Carolyn M.
    BMJ NEUROLOGY OPEN, 2024, 6 (02)
  • [50] Detection of mitochondrial defects in patients with mitochondrial diseases: A case study
    Lemieux, Helene
    Rosca, Mariana G.
    Vazquez, Edwin J.
    Kehres, David
    Gnaiger, Erich
    Hoppel, Charles L.
    MITOCHONDRION, 2010, 10 (02) : 237 - 238