A Preliminary Videofluoroscopic Investigation of Swallowing Physiology and Function in Individuals with Oculopharyngeal Muscular Dystrophy (OPMD)

被引:0
|
作者
Ashley A. Waito
Catriona M. Steele
Melanie Peladeau-Pigeon
Angela Genge
Zohar Argov
机构
[1] Toronto Rehabilitation Institute - University Health Network,Swallowing Rehabilitation Research Laboratory
[2] University of Toronto,Rehabilitation Sciences Institute
[3] McGill University,Montreal Neurological Institute and Hospital
[4] BioBlast Pharma Ltd.,undefined
来源
Dysphagia | 2018年 / 33卷
关键词
Deglutition disorders; Oculopharyngeal muscular dystrophy; Videofluoroscopy; Aspiration; Post-swallow residue; Swallow kinematics; Swallow timing;
D O I
暂无
中图分类号
学科分类号
摘要
Dysphagia is one of the primary symptoms experienced by individuals with Oculopharyngeal Muscular Dystrophy (OPMD). However, we lack understanding of the discrete changes in swallowing physiology that are seen in OPMD, and the resulting relationship to impairments of swallowing safety and efficiency. This study sought to describe the pathophysiology of dysphagia in a small sample of patients with OPMD using a videofluoroscopy examination (VFSS) involving 3 × 5 mL boluses of thin liquid barium (22% w/v). The aim of this study is to extend what is known about the pathophysiology of dysphagia in OPMD, by quantifying changes in swallow timing, kinematics, safety, and efficiency, measured from VFSS. This study is a secondary analysis of baseline VFSS collected from 11 adults (4 male), aged 48–62 (mean 57) enrolled in an industry-sponsored phase 2 therapeutic drug trial. Blinded raters scored the VFSS recordings for safety [Penetration-Aspiration Scale (PAS)], efficiency [Normalized Residue Ratio Scale (NRRS)], timing [Pharyngeal Transit Time (PTT), Swallow Reaction Time (SRT), Laryngeal Vestibule Closure Reaction Time (LVCrt), Upper Esophageal Sphincter Opening Duration (UESD)], and kinematics (hyoid movement, pharyngeal constriction, UES opening width). Impairment thresholds from existing literature were defined to characterize swallowing physiology and function. Further, Fisher’s Exact tests and Pearson’s correlations were used to conduct a preliminary exploration of associations between swallowing physiology (e.g., kinematics, timing) and function (i.e., safety, efficiency). Compared to published norms, we identified significant differences in the degree of maximum pharyngeal constriction, hyoid movement distance and speed, as well as degree and timeliness of airway closure. Unsafe swallowing (PAS ≥ 3) was seen in only 3/11 patients. By contrast, clinically significant residue (i.e., NRRS scores ≥ 0.09 vallecular; ≥ 0.2 pyriform) was seen in 7/11 patients. Fisher’s Exact tests revealed associations between prolonged SRT, PTT, and unsafe swallowing. Weak associations were also identified between post-swallow residue and poor pharyngeal constriction during the swallow. Detailed analysis of swallowing physiology in this series of adults with OPMD aligns with impaired muscular function (e.g., reduced pharyngeal constriction, incomplete laryngeal vestibule closure) associated with the disease, and primary functional challenges with swallow efficiency. Further work is needed to explore a greater range of food and liquid textures, and to identify additional physiological mechanisms underlying swallowing impairment in OPMD.
引用
收藏
页码:789 / 802
页数:13
相关论文
共 50 条
  • [1] A Preliminary Videofluoroscopic Investigation of Swallowing Physiology and Function in Individuals with Oculopharyngeal Muscular Dystrophy (OPMD)
    Waito, Ashley A.
    Steele, Catriona M.
    Peladeau-Pigeon, Melanie
    Genge, Angela
    Argov, Zohar
    DYSPHAGIA, 2018, 33 (06) : 789 - 802
  • [2] Oculopharyngeal muscular dystrophy (OPMD)
    Neetens, A
    Martin, JJ
    Brais, B
    Wein, B
    Dreuw, B
    Tijssen, CC
    Ceuterick, C
    NEURO-OPHTHALMOLOGY, 1997, 17 (04) : 189 - 200
  • [3] Capturing disease progression in oculopharyngeal muscular dystrophy (OPMD)
    Kroon, R.
    Kalf, J.
    de Swart, B.
    Horlings, C.
    van Engelen, B.
    NEUROMUSCULAR DISORDERS, 2019, 29 : S139 - S139
  • [4] Characteristics and natural history of oculopharyngeal muscular dystrophy (OPMD): The study protocol of 'OPMD Forte'
    Kroon, H.
    Kalf, J.
    de Swart, B.
    Horlings, C.
    van Engelen, B.
    NEUROMUSCULAR DISORDERS, 2016, 26 : S139 - S140
  • [5] Haplotype analysis of oculopharyngeal muscular dystrophy (OPMD) locus in Yakutia
    Marusin, A. V.
    Kurtanov, H. A.
    Maksimova, N. R.
    Swarovsakaja, M. G.
    Stepanov, V. A.
    RUSSIAN JOURNAL OF GENETICS, 2016, 52 (03) : 331 - 338
  • [6] Clinical characteristics of patients with oculopharyngeal muscular dystrophy (OPMD) in Israel
    Greenbaum, Lior
    Ben-David, Merav
    Zvulunov, Alex
    Dori, Amir
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2024, 32 : 1102 - 1103
  • [7] Clinical characteristics of patients with oculopharyngeal muscular dystrophy (OPMD) in Israel
    Greenbaum, Lior
    Ben-David, Merav
    Zvulunov, Alex
    Dori, Amir
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2024, 32 : 1102 - 1103
  • [8] Swallowing in myotonic muscular dystrophy: A videofluoroscopic study
    Leonard, RJ
    Kendall, KA
    Johnson, R
    McKenzie, S
    ARCHIVES OF PHYSICAL MEDICINE AND REHABILITATION, 2001, 82 (07): : 979 - 985
  • [9] Oculopharyngeal Muscular Dystrophy (OPMD): A Good Candidate for Myoblast Transplantation
    Butler-Browne, Gillian
    Perie, Sophie
    Mamchaoui, Kamel
    Bouazza, Belaid
    Larghero, Jerome
    Mouly, Vincent
    St Guily, Jean Lacau
    HUMAN GENE THERAPY, 2009, 20 (06) : 660 - 660
  • [10] Haplotype analysis of oculopharyngeal muscular dystrophy (OPMD) locus in Yakutia
    A. V. Marusin
    H. A. Kurtanov
    N. R. Maksimova
    M. G. Swarovsakaja
    V. A. Stepanov
    Russian Journal of Genetics, 2016, 52 : 331 - 338