Better global and cognitive functioning in choreatic versus hypokinetic-rigid Huntington's disease

被引:29
作者
Hart, Ellen P. [1 ]
Marinus, Johan [1 ]
Burgunder, Jean-Marc [2 ]
Bentivoglio, Anna Rita [3 ]
Craufurd, David [4 ,5 ]
Reilmann, Ralf [6 ]
Saft, Carsten [7 ]
Roos, Raymund A. C. [1 ]
机构
[1] Leiden Univ, Med Ctr, Dept Neurol, NL-2300 RC Leiden, Netherlands
[2] Univ Bern, Dept Neurol, Bern, Switzerland
[3] Univ Cattolica Sacro Cuore, Dept Neurol, Rome, Italy
[4] Univ Manchester, Manchester Acad Hlth Sci Ctr, Manchester, Lancs, England
[5] Cent Manchester Univ Hosp NHS Fdn Trust, Manchester, Lancs, England
[6] Univ Munster, Dept Neurol, Munster, Germany
[7] Ruhr Univ Bochum, Dept Neurol, Bochum, Germany
关键词
Huntington's disease; hyperkinetic; hypokinetic; cognition; chorea; PARKINSONS-DISEASE; MOTOR; BRADYKINESIA; DISABILITY; VENEZUELA; FEATURES; DECLINE;
D O I
10.1002/mds.25422
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background Understanding the relation between predominantly choreatic and hypokinetic-rigid motor subtypes and cognitive and general functioning may contribute to knowledge about different motor phenotypes in Huntington's disease. Methods In the European Huntington's Disease Network Registry study, 1882 subjects were classified as being predominantly choreatic (n=528) or hypokinetic-rigid (n=432), according to their scores on items of the total motor score a priori labeled as choreatic or hypokinetic-rigid; the other 922 patients were of a mixed type. The relationship between motor type and cognitive (verbal fluency, symbol digit modalities, Stroop color, word and interference tests) and functional (total functional capacity) capacity was investigated using multiple linear regression. Results Motor subtype contributed significantly to the total functional capacity score (partial r(2): 7.8%; P<.001) and to the 5 cognitive scores (partial r(2) ranged from 2.0% to 8.4%; all P<.001). Conclusions Patients with a predominantly choreatic motor phenotype performing better in all areas than patients with a hypokinetic-rigid motor phenotype. (c) 2013 Movement Disorder Society
引用
收藏
页码:1142 / 1145
页数:4
相关论文
共 21 条
[1]   CLINICAL CORRELATES OF DEMENTIA AND DISABILITY IN HUNTINGTONS-DISEASE [J].
BRANDT, J ;
STRAUSS, ME ;
LARUS, J ;
JENSEN, B ;
FOLSTEIN, SE ;
FOLSTEIN, MF .
JOURNAL OF CLINICAL NEUROPSYCHOLOGY, 1984, 6 (04) :401-412
[2]   Tetrabenazine: the first approved drug for the treatment of chorea in US patients with Huntington disease [J].
Frank, Samuel .
NEUROPSYCHIATRIC DISEASE AND TREATMENT, 2010, 6 :657-665
[3]   RELATIONSHIP BETWEEN MOTOR AND COGNITIVE DISORDERS IN HUNTINGTONS-DISEASE [J].
GIROTTI, F ;
MARANO, R ;
SOLIVERI, P ;
GEMINIANI, G ;
SCIGLIANO, G .
JOURNAL OF NEUROLOGY, 1988, 235 (08) :454-457
[4]   VARIABLE EXPRESSION OF PARKINSONS-DISEASE - A BASE-LINE ANALYSIS OF THE DATATOP COHORT [J].
JANKOVIC, J ;
MCDERMOTT, M ;
CARTER, J ;
GAUTHIER, S ;
GOETZ, C ;
GOLBE, L ;
HUBER, S ;
KOLLER, W ;
OLANOW, C ;
SHOULSON, I ;
STERN, M ;
TANNER, C ;
WEINER, W .
NEUROLOGY, 1990, 40 (10) :1529-1534
[5]   Unified Huntington's disease rating scale: Reliability and consistency [J].
Kieburtz, K ;
Penney, JB ;
Como, P ;
Ranen, N ;
Shoulson, I ;
Feigin, A ;
Abwender, D ;
Greenamyre, JT ;
Higgins, D ;
Marshall, FJ ;
Goldstein, J ;
Steinberg, K ;
Shih, C ;
Richard, I ;
Hickey, C ;
Zimmerman, C ;
Orme, C ;
Claude, K ;
Oakes, D ;
Sax, DS ;
Kim, A ;
Hersch, S ;
Jones, R ;
Auchus, A ;
Olsen, D ;
BisseyBlack, C ;
Rubin, A ;
Schwartz, R ;
Dubinsky, R ;
Mallonee, W ;
Gray, C ;
Godfrey, N ;
Suter, G ;
Shannon, KM ;
Stebbins, GT ;
Jaglin, JA ;
Marder, K ;
Taylor, S ;
Louis, E ;
Moskowitz, C ;
Thorne, D ;
Zubin, N ;
Wexler, N ;
Swenson, MR ;
Paulsen, J ;
Swerdlow, N ;
Albin, R ;
Wernette, C ;
Walker, F ;
Hunt, V .
MOVEMENT DISORDERS, 1996, 11 (02) :136-142
[6]   The relationship between impairment of voluntary movements and cognitive impairment in Huntington's disease [J].
Klempir, Jiri ;
Klempirova, Olga ;
Stochl, Jan ;
Spackova, Natasa ;
Roth, Jan .
JOURNAL OF NEUROLOGY, 2009, 256 (10) :1629-1633
[7]   A NOVEL GENE CONTAINING A TRINUCLEOTIDE REPEAT THAT IS EXPANDED AND UNSTABLE ON HUNTINGTONS-DISEASE CHROMOSOMES [J].
MACDONALD, ME ;
AMBROSE, CM ;
DUYAO, MP ;
MYERS, RH ;
LIN, C ;
SRINIDHI, L ;
BARNES, G ;
TAYLOR, SA ;
JAMES, M ;
GROOT, N ;
MACFARLANE, H ;
JENKINS, B ;
ANDERSON, MA ;
WEXLER, NS ;
GUSELLA, JF ;
BATES, GP ;
BAXENDALE, S ;
HUMMERICH, H ;
KIRBY, S ;
NORTH, M ;
YOUNGMAN, S ;
MOTT, R ;
ZEHETNER, G ;
SEDLACEK, Z ;
POUSTKA, A ;
FRISCHAUF, AM ;
LEHRACH, H ;
BUCKLER, AJ ;
CHURCH, D ;
DOUCETTESTAMM, L ;
ODONOVAN, MC ;
RIBARAMIREZ, L ;
SHAH, M ;
STANTON, VP ;
STROBEL, SA ;
DRATHS, KM ;
WALES, JL ;
DERVAN, P ;
HOUSMAN, DE ;
ALTHERR, M ;
SHIANG, R ;
THOMPSON, L ;
FIELDER, T ;
WASMUTH, JJ ;
TAGLE, D ;
VALDES, J ;
ELMER, L ;
ALLARD, M ;
CASTILLA, L ;
SWAROOP, M .
CELL, 1993, 72 (06) :971-983
[8]   Huntington's disease - Clinical correlates of disability and progression [J].
Mahant, N ;
McCusker, EA ;
Byth, K ;
Graham, S .
NEUROLOGY, 2003, 61 (08) :1085-1092
[9]   Juvenile onset Huntington's disease - Clinical and research perspectives [J].
Nance, MA ;
Myers, RH .
MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS, 2001, 7 (03) :153-157
[10]   HUNTINGTONS-DISEASE IN VENEZUELA - 7 YEARS OF FOLLOW-UP ON SYMPTOMATIC AND ASYMPTOMATIC INDIVIDUALS [J].
PENNEY, JB ;
YOUNG, AB ;
SHOULSON, I ;
STAROSTARUBENSTEIN, S ;
SNODGRASS, SR ;
SANCHEZRAMOS, J ;
RAMOSARROVO, M ;
GOMEZ, F ;
PENCHASZADEH, G ;
ALVIR, J ;
ESTEVES, J ;
DEQUIROZ, I ;
MARSOL, N ;
MORENO, H ;
CONNEALLY, PM ;
BONILLA, E ;
WEXLER, NS .
MOVEMENT DISORDERS, 1990, 5 (02) :93-99