Extragenetic factors and clinical penetrance of DYT1 dystonia: an exploratory study

被引:25
|
作者
Martino, D. [1 ,2 ]
Gajos, A. [3 ]
Gallo, V. [4 ,5 ]
Cif, L. [6 ,7 ,8 ,9 ,10 ]
Coubes, P. [6 ,7 ,8 ,9 ,10 ]
Tinazzi, M. [11 ]
Schneider, S. A. [12 ,13 ]
Fiorio, M. [11 ]
Zorzi, G. [14 ]
Nardocci, N. [14 ]
Ben-Shlomo, Y. [15 ]
Edwards, M. J. [12 ]
Bhatia, K. P. [12 ]
机构
[1] Queen Mary Univ London, Barts & London Sch Med & Dent, Neurosci & Trauma Ctr, London, England
[2] South London NHS Trust, Queen Elizabeth Hosp, London, England
[3] Med Univ Lodz, Dept Extrapyramidal Dis, Lodz, Poland
[4] Univ London Imperial Coll Sci Technol & Med, Sch Publ Hlth, Dept Epidemiol & Biostat, London, England
[5] London Sch Hyg & Trop Med, London WC1, England
[6] Hop Gui de Chauliac, CHRU Montpellier, Dept Neurochirurg, F-34000 Montpellier, France
[7] URMA, Montpellier, France
[8] INSERM, U661, F-34000 Montpellier, France
[9] Univ Montpellier I, F-34000 Montpellier, France
[10] CNRS, Inst Genom Fonct, UMR5203, F-34000 Montpellier, France
[11] Univ Verona, Dipartimento Sci Neurol Neuropsicol Morfol & Moto, I-37100 Verona, Italy
[12] UCL Inst Neurol, Sobell Dept Motor Neurosci & Movement Disorders, London WC1N 3BG, England
[13] Med Univ Lubeck, Dept Neurol, Schilling Sect Clin & Mol Neurogenet, D-23568 Lubeck, Germany
[14] Fdn IRCCS Ist Neurol C Besta, Dept Child Neurol, Milan, Italy
[15] Univ Bristol, Sch Social & Community Med, Bristol, Avon, England
关键词
Dystonia; Epidemiology; Neuroepidemiology; Clinical neurology; Movement disorders; DELAYED-ONSET DYSTONIA; PARKINSONS-DISEASE; INFECTION; ASPHYXIA;
D O I
10.1007/s00415-012-6765-2
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Factors modifying the clinical penetrance of DYT1 dystonia are incompletely defined. Particularly, the contribution of extragenetic factors has been subject to only limited investigation and remains largely unexplored. A possible effect of childhood infections has been proposed, and the effect of other factors, such as perinatal adversity and trauma, has not been systematically investigated. We performed an exploratory analysis of the exposure to perinatal adversity, childhood infections, general anaesthesia and trauma comparing 39 manifesting carriers of the a dagger GAG mutation, 23 non-manifesting carriers and 48 non-carriers from a multi-centre European series of 28 families with DYT1 dystonia, by means of a self-completed questionnaire and clinical interview. Detailed information on perinatal adversities (pre-term birth, complications at natural delivery, urgent caesarean section), previous childhood infections, and prior general anaesthesia or physical trauma was recorded. A positive association between a history of complications of vaginal delivery and manifestation of dystonia was detected, which was not confounded by age, gender, or education level (odds ratio 8.47, 95 % confidence interval 1.45-49.4, p = 0.02). We could not observe any significant association between presence of dystonia and the other investigated variables. Comparing non-manifesting carriers to non-carriers, the presence of the a dagger GAG mutation per se was not associated with any of the environmental exposures explored. Perinatal adversities might modulate the clinical penetrance of DYT1 dystonia; their interaction with known genetic factors modifying penetrance of this condition should be investigated in new, larger collaborative studies.
引用
收藏
页码:1081 / 1086
页数:6
相关论文
共 50 条
  • [31] Clinical characteristics of carriers of a GAG deletion in the DYT1 gene amongst Polish patients with primary dystonia
    Szczaluba, K.
    Jurek, M.
    Milewski, M.
    Friedman, A.
    Kadziolka, B.
    Szolna, A.
    Bal, J.
    Mazurczak, T.
    EUROPEAN JOURNAL OF NEUROLOGY, 2007, 14 (06) : 659 - 662
  • [32] Impaired motor learning in mice expressing TorsinA with the DYT1 dystonia mutation
    Sharma, N
    Baxter, MG
    Petravicz, J
    Bragg, DC
    Schienda, A
    Standaert, DG
    Breakefield, XO
    JOURNAL OF NEUROSCIENCE, 2005, 25 (22) : 5351 - 5355
  • [33] The abnormal firing of Purkinje cells in the knockin mouse model of DYT1 dystonia
    Liu, Yuning
    Xing, Hong
    Wilkes, Bradley J.
    Yokoi, Fumiaki
    Chen, Huanxin
    Vaillancourt, David E.
    Li, Yuqing
    BRAIN RESEARCH BULLETIN, 2020, 165 : 14 - 22
  • [34] Unusual phenotypes in DYT1 dystonia: A report of five cases and a review of the literature
    Edwards, M
    Wood, N
    Bhatia, K
    MOVEMENT DISORDERS, 2003, 18 (06) : 706 - 711
  • [35] Microfluidic platform to evaluate migration of cells from patients with DYT1 dystonia
    Nery, Flavia C.
    da Hora, Cintia C.
    Atai, Nadia A.
    Kim, Edward Y.
    Hettich, Jasmin
    Mempel, Thorsten R.
    Breakefield, Xandra O.
    Irimia, Daniel
    JOURNAL OF NEUROSCIENCE METHODS, 2014, 232 : 181 - 188
  • [36] Diminishing evidence for torsinA-positive neuronal inclusions in DYT1 dystonia
    Pratt, Drew
    Mente, Karin
    Rahimpour, Shervin
    Edwards, Nancy A.
    Tinaz, Sule
    Berman, Brian D.
    Hallett, Mark
    Ray-Chaudhury, Abhik
    ACTA NEUROPATHOLOGICA COMMUNICATIONS, 2016, 4
  • [37] Pallidal Stimulation in Children: Comparison Between Cerebral Palsy and DYT1 Dystonia
    Marks, Warren
    Bailey, Laurie
    Reed, MaryAnn
    Pomykal, Angela
    Mercer, Mary
    Macomber, David
    Acosta, Fernando, Jr.
    Honeycutt, John
    JOURNAL OF CHILD NEUROLOGY, 2013, 28 (07) : 840 - 848
  • [38] Diminishing evidence for torsinA-positive neuronal inclusions in DYT1 dystonia
    Drew Pratt
    Karin Mente
    Shervin Rahimpour
    Nancy A. Edwards
    Sule Tinaz
    Brian D. Berman
    Mark Hallett
    Abhik Ray-Chaudhury
    Acta Neuropathologica Communications, 4
  • [39] Electromyographic evidence in support of a knock-in mouse model of DYT1 Dystonia
    DeAndrade, Mark P.
    Trongnetrpunya, Amy
    Yokoi, Fumiaki
    Cheetham, Chad C.
    Peng, Ning
    Wyss, J. Michael
    Ding, Mingzhou
    Li, Yuqing
    MOVEMENT DISORDERS, 2016, 31 (11) : 1633 - 1639
  • [40] Deep Brain Stimulation in DYT1 Dystonia: A 10-Year Experience
    Panov, Fedor
    Gologorsky, Yakov
    Connors, Grayson
    Tagliati, Michele
    Miravite, Joan
    Alterman, Ron L.
    NEUROSURGERY, 2013, 73 (01) : 86 - 93