Brain MRI hippocampal of clinical status in a mild volume and prediction cognitive impairment trial

被引:114
作者
Grundman, M
Sencakova, D
Jack, CR
Petersen, RC
Kim, HT
Schultz, A
Weiner, MF
DeCarli, C
DeKosky, ST
van Dyck, C
Thomas, RG
Thomas, RG
Thal, LJ
机构
[1] Univ Calif San Diego, Dept Neurosci, La Jolla, CA 92093 USA
[2] Mayo Clin & Mayo Fdn, Dept Diagnost Radiol, Rochester, MN 55905 USA
[3] Mayo Clin & Mayo Fdn, Dept Neurol, Rochester, MN 55905 USA
[4] Univ Texas, SW Med Ctr, Dept Psychiat, Dallas, TX USA
[5] Univ Calif Davis, Dept Neurol, Davis, CA 95616 USA
[6] Univ Pittsburgh, Dept Neurol, Pittsburgh, PA 15260 USA
[7] Yale Univ, Sch Med, Dept Psychiat, New Haven, CT USA
关键词
mild cognitive impairment; clinical trial; MRI; hippocampal volume; Alzheimer's disease;
D O I
10.1007/s12031-002-0006-6
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Mild Cognitive Impairment (MCI) is considered a transitional stage in the pathogenesis of Alzheimer's disease; however, not all MCI patients progress to clinically defined AD or decline at identical rates. Hippocampal atrophy, as measured by Magnetic Resonance Imaging (MRI), may be a marker for hippocampal pathology in patients with MCI and predict a more rapid deterioration to clinical AD. In this study, we used MRI data from an ongoing MCI clinical trial to determine whether MRI hippocampal volume at baseline was associated with cognitive and functional performance in MCI subjects and whether it predicted those individuals who were more likely to develop AD. We performed correlational analyses between the MRI hippocampal volumes at study entry and the subjects' concurrent performance on neuropsychological measures and clinical ratings. Larger hippocampal volume was associated with better performance on tests of memory, general cognition, and overall clinical ratings. Further analyses suggested that a smaller baseline hippocampal volume may be associated with a higher risk of developing clinical AD. As the trial is still ongoing, these results require confirmation once the trial is completed. In summary, these data suggest that MRI hippocampal volume may be a useful correlate of disease severity in MCI subjects and a prognostic indicator of subsequent AD.
引用
收藏
页码:23 / 27
页数:5
相关论文
共 10 条
[1]   MINI-MENTAL STATE - PRACTICAL METHOD FOR GRADING COGNITIVE STATE OF PATIENTS FOR CLINICIAN [J].
FOLSTEIN, MF ;
FOLSTEIN, SE ;
MCHUGH, PR .
JOURNAL OF PSYCHIATRIC RESEARCH, 1975, 12 (03) :189-198
[2]  
Grundman M., 1996, Neurology, V46, pA403
[3]   Medial temporal atrophy on MRI in normal aging and very mild Alzheimer's disease [J].
Jack, CR ;
Petersen, RC ;
Xu, YC ;
Waring, SC ;
OBrien, PC ;
Tangalos, EG ;
Smith, GE ;
Ivnik, RJ ;
Kokmen, E .
NEUROLOGY, 1997, 49 (03) :786-794
[4]   Rates of hippocampal atrophy correlate with change in clinical status in aging and AD [J].
Jack, CR ;
Petersen, RC ;
Xu, Y ;
O'Brien, PC ;
Smith, GE ;
Ivnik, RJ ;
Boeve, BF ;
Tangalos, EG ;
Kokmen, E .
NEUROLOGY, 2000, 55 (04) :484-489
[5]   Prediction of AD with MRI-based hippocampal volume in mild cognitive impairment [J].
Jack, CR ;
Petersen, RC ;
Xu, YC ;
O'Brien, PC ;
Smith, GE ;
Ivnik, RJ ;
Boeve, BF ;
Waring, SC ;
Tangalos, EG ;
Kokmen, E .
NEUROLOGY, 1999, 52 (07) :1397-1403
[6]   MR IMAGING-BASED VOLUME MEASUREMENTS OF THE HIPPOCAMPAL-FORMATION AND ANTERIOR TEMPORAL-LOBE - VALIDATION STUDIES [J].
JACK, CR ;
BENTLEY, MD ;
TWOMEY, CK ;
ZINSMEISTER, AR .
RADIOLOGY, 1990, 176 (01) :205-209
[7]  
Morris J C, 1997, Int Psychogeriatr, V9 Suppl 1, P173, DOI 10.1017/S1041610297004870
[8]   APOLIPOPROTEIN-E STATUS AS A PREDICTOR OF THE DEVELOPMENT OF ALZHEIMERS-DISEASE IN MEMORY-IMPAIRED INDIVIDUALS [J].
PETERSEN, RC ;
SMITH, GE ;
IVNIK, RJ ;
TANGALOS, EG ;
SCHAID, DJ ;
THIBODEAU, SN ;
KOKMEN, E ;
WARING, SC ;
KURLAND, LT .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1995, 273 (16) :1274-1278
[9]   Mild cognitive impairment - Clinical characterization and outcome [J].
Petersen, RC ;
Smith, GE ;
Waring, SC ;
Ivnik, RJ ;
Tangalos, EG ;
Kokmen, E .
ARCHIVES OF NEUROLOGY, 1999, 56 (03) :303-308
[10]  
ROSEN WG, 1984, AM J PSYCHIAT, V141, P1356