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
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