Future therapies of Tourette syndrome

被引:11
作者
Chappell, PB
Scahill, LD
Leckman, JF
机构
[1] YALE UNIV,SCH MED,DEPT NURSING,NEW HAVEN,CT
[2] YALE UNIV,SCH MED,DEPT PEDIAT,NEW HAVEN,CT 06510
[3] YALE UNIV,SCH MED,YALE CHILD STUDY CTR,NEW HAVEN,CT
关键词
D O I
10.1016/S0733-8619(05)70324-8
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Currently available pharmacologic therapies for Tourette syndrome often are characterized by limited effectiveness and unacceptable side effect profiles. In recent years, however, a series of new approaches have emerged which may lead to novel, more effective, and better tolerated treatments of tics and associated behavioral problems. Especially promising is the wide range of new atypical antipsychotic medications with unique and diverse receptor affinity profiles that are entering clinical practice. Over the next few years, intensive research efforts will be required to characterize the effect of the new atypical antipsychotics in patients with Tourette syndrome and related disorders, and to determine which sets of symptoms and which subgroups of patients best respond to particular agents. In the near future, corticotropin releasing factor antagonists and agents which act on excitatory amino acid neurotransmitter systems also will become available and may provide treatment interventions, which theoretically could alter the long term course and outcome of Tourette syndrome. In addition, nonpharmacologic interventions, such as immunologic and behavior therapies, are receiving increasing attention and may provide an alternative or supplement to medication for selected subgroups of Tourette syndrome patients.
引用
收藏
页码:429 / &
页数:24
相关论文
共 102 条
[1]   Perioperative use of botulinum toxin for movement disorder-induced cervical spine disease [J].
Adler, CH ;
Zimmerman, RS ;
Lyons, MK ;
Simeone, F ;
Brin, MF .
MOVEMENT DISORDERS, 1996, 11 (01) :79-81
[2]   CASE-STUDY - A NEW INFECTION-TRIGGERED, AUTOIMMUNE SUBTYPE OF PEDIATRIC OCD AND TOURETTES-SYNDROME [J].
ALLEN, AJ ;
LEONARD, HL ;
SWEDO, SE .
JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY, 1995, 34 (03) :307-311
[3]  
ANDERSON GM, 1992, ADV NEUROL, V58, P123
[4]  
[Anonymous], 1993, Applied and Preventive Psychology, DOI [DOI 10.1016/S0962-1849(05)80093-9, 10.1016/S0962-1849(05)80093-9]
[5]   ALPHA-2 ADRENERGIC AGONISTS DECREASE DISTRACTIBILITY IN AGED MONKEYS PERFORMING THE DELAYED-RESPONSE TASK [J].
ARNSTEN, AFT ;
CONTANT, TA .
PSYCHOPHARMACOLOGY, 1992, 108 (1-2) :159-169
[6]  
Arnsten AFT, 1996, ARCH GEN PSYCHIAT, V53, P448
[7]  
Arnt J., 1993, Society for Neuroscience Abstracts, V19, P383
[8]   HABIT-REVERSAL - METHOD OF ELIMINATING NERVOUS HABITS AND TICS [J].
AZRIN, NH ;
NUNN, RG .
BEHAVIOUR RESEARCH AND THERAPY, 1973, 11 (04) :619-628
[9]   GUANFACINE AS AN ALPHA-2-AGONIST INDUCER OF GROWTH-HORMONE SECRETION - A COMPARISON WITH CLONIDINE [J].
BALLDIN, J ;
BERGGREN, U ;
ERIKSSON, E ;
LINDSTEDT, G ;
SUNDKLER, A .
PSYCHONEUROENDOCRINOLOGY, 1993, 18 (01) :45-55
[10]   Olanzapine versus placebo and haloperidol - Acute phase results of the North American double-blind olanzapine trial [J].
Beasley, CM ;
Tollefson, G ;
Tran, P ;
Satterlee, W ;
Sanger, T ;
Hamilton, S ;
Fabre, L ;
Small, J ;
Ereshefsky, L ;
True, J ;
Nemeroff, C ;
Risch, SC ;
Perry, PJ ;
Potkin, SG ;
Borison, RL ;
James, S ;
Meltzer, HY ;
Iqbal, N ;
Fann, WE ;
Gewirtz, GR ;
Landbloom, R ;
RoyByrne, PP ;
Tuason, VB ;
Carman, JS ;
Stokes, PE ;
Williams, R ;
Ancill, RJ ;
MacEwan, GW ;
Gujavarty, KS ;
Jones, B ;
Lohr, JB .
NEUROPSYCHOPHARMACOLOGY, 1996, 14 (02) :111-123