Nature and frequency of respiratory involvement in chronic progressive external ophthalmoplegia

被引:11
作者
Smits, Bart W. [1 ]
Heijdra, Yvonne F. [2 ]
Cuppen, Femke W. A. [2 ]
van Engelen, Baziel G. M. [1 ]
机构
[1] Radboud Univ Nijmegen, Med Ctr, Dept Neurol, Neuromuscular Ctr Nijmegen, NL-6500 HB Nijmegen, Netherlands
[2] Radboud Univ Nijmegen, Med Ctr, Dept Pulm Dis, NL-6500 HB Nijmegen, Netherlands
关键词
Chronic progressive external ophthalmoplegia; Kearns-Sayre syndrome; Respiratory muscles; Pneumonia; Polymerase gamma; KEARNS-SAYRE-SYNDROME; MUSCLE FUNCTION; DISEASES; LUNG;
D O I
10.1007/s00415-011-6060-7
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Chronic progressive external ophthalmoplegia (CPEO) is a relatively common mitochondrial disorder. Weakness of the extra-ocular, limb girdle and laryngeal muscles are established clinical features. Respiratory muscle involvement however has never been studied systematically, even though respiratory complications are one of the main causes of death. We therefore determined the prevalence and nature of respiratory muscle involvement in 23 patients with genetically confirmed CPEO. The main finding was decreased respiratory muscle strength, both expiratory (76.8% of predicted, p = 0.002) and inspiratory (79.5% of predicted, p = 0.004). Although the inspiratory vital capacity (92.5% of predicted, p = 0.021) and the forced expiratory volume in 1 s (89.3% of predicted, p = 0.002) were below predicted values, both were still within the normal range in the majority of patients. Expiratory weakness was associated with a decreased vital capacity (rho = 0.502, p = 0.015) and decreased peak expiratory flow (rho = 0.422, p = 0.045). Moreover, expiratory muscle strength was lower in patients with limb girdle weakness (62.6 +/- A 26.1% of predicted vs. 98.9 +/- A 22.5% in patients with normal limb girdle strength, p = 0.003), but was not associated with other clinical features, subjective respiratory complaints, disease severity or disease duration. Since respiratory involvement in CPEO is associated with severe morbidity and mortality, the present data justify periodic assessment of respiratory functions in all CPEO patients.
引用
收藏
页码:2020 / 2025
页数:6
相关论文
共 24 条
  • [1] Prevalence and progression of mitochondrial diseases:: A study of 50 patients
    Arpa, J
    Cruz-Martínez, A
    Campos, Y
    Gutiérrez-Molina, M
    García-Rio, F
    Pérez-Conde, C
    Martín, MA
    Rubio, JC
    Del Hoyo, P
    Arpa-Fernández, A
    Arenas, J
    [J]. MUSCLE & NERVE, 2003, 28 (06) : 690 - 695
  • [2] Chronic progressive ophthalmoplegia with large-scale mtDNA rearrangement:: can we predict progression?
    Aure, Karine
    de Baulny, Helene Ogier
    Laforet, Pascal
    Jardel, Claude
    Eymard, Bruno
    Lombes, Anne
    [J]. BRAIN, 2007, 130 : 1516 - 1524
  • [3] RECURRENT RESPIRATORY INSUFFICIENCY AND DEPRESSED VENTILATORY DRIVE COMPLICATING MITOCHONDRIAL MYOPATHIES
    BAROHN, RJ
    CLANTON, T
    SAHENK, Z
    MENDELL, JR
    [J]. NEUROLOGY, 1990, 40 (01) : 103 - 106
  • [4] Chronic Progressive External Ophthalmoplegia - Symptom or Syndrome?
    Bau, V.
    Deschauer, M.
    Zierz, S.
    [J]. KLINISCHE MONATSBLATTER FUR AUGENHEILKUNDE, 2009, 226 (10) : 822 - 828
  • [5] Bindoff L, 1997, MITOCHONDRIAL MYOPAT, P85
  • [6] RESPIRATORY MUSCLE AND PULMONARY-FUNCTION IN POLYMYOSITIS AND OTHER PROXIMAL MYOPATHIES
    BRAUN, NMT
    ARORA, NS
    ROCHESTER, DF
    [J]. THORAX, 1983, 38 (08) : 616 - 623
  • [7] DEPRESSED VENTILATORY RESPONSE IN OCULOCRANIOSOMATIC NEUROMUSCULAR DISEASE
    CARROLL, JE
    ZWILLICH, C
    WEIL, JV
    BROOKE, MH
    [J]. NEUROLOGY, 1976, 26 (02) : 140 - 146
  • [8] DESNUELLE C, 1988, Neurology, V38, P102
  • [9] Sensory ataxic neuropathy as the presenting feature of a novel mitochondrial disease
    Fadic, R
    Russell, JA
    Vedanarayanan, VV
    Lehar, M
    Kuncl, RW
    Johns, DR
    [J]. NEUROLOGY, 1997, 49 (01) : 239 - 245
  • [10] HEIJDRA YF, 1993, EUR RESPIR J, V6, P541