Journal of the Neurological Sciences
Volume 201, Issue 1 , Pages 19-25, 15 September 2002

Longitudinal analysis of abnormal domains comprising mild cognitive impairment (MCI) during aging

  • John S Meyer

      Affiliations

    • Corresponding Author InformationCorresponding author. Cerebrovascular Research Laboratory, Veterans Administration Medical Center, Building 110, Room 225, 2002 Holcombe Boulevard, 151A, Houston, TX 77030, USA. Tel.: +1-713-795-5807; fax: +1-713-794-7583
    • Department of Neurology, Baylor College of Medicine, Houston, TX, USA
    • Cerebrovascular Research Laboratory, Veterans Administration Medical Center, Houston, TX, USA
  • ,
  • Gelin Xu

      Affiliations

    • Department of Neurology, Baylor College of Medicine, Houston, TX, USA
    • Cerebrovascular Research Laboratory, Veterans Administration Medical Center, Houston, TX, USA
  • ,
  • John Thornby

      Affiliations

    • Department of Family and Community Medicine, Baylor College of Medicine, Houston, TX, USA
    • Biostatistical Laboratory, Veterans Administration Medical Center, Houston, TX, USA
  • ,
  • Munir Chowdhury

      Affiliations

    • Department of Neurology, Baylor College of Medicine, Houston, TX, USA
    • Cerebrovascular Research Laboratory, Veterans Administration Medical Center, Houston, TX, USA
  • ,
  • Minh Quach

      Affiliations

    • Department of Neurology, Baylor College of Medicine, Houston, TX, USA
    • Cerebrovascular Research Laboratory, Veterans Administration Medical Center, Houston, TX, USA

Received 20 February 2002; received in revised form 20 May 2002; accepted 21 May 2002.

Abstract 

Research directed towards early diagnosis and therapy of dementia demands rapid identification of prodromal mild cognitive impairment (MCI). A longitudinal study was designed to clarify whether different domains of cognitive impairment, tested by Mini-Mental State Examination (MMSE), help predict dementia. After 3.74±2.94 years of follow-up among 291 cognitively normative volunteers, 73 developed MCI. During the next 3.88±3.01 years of MCI follow-up, 47.9% of MCI developed dementia of Alzheimer's type (DAT), 20.5% of MCI developed vascular dementia (VaD) and 31.5% maintained persistent MCI at the time of data analysis. Total MMSE and subtest scores analyzed at MCI onset showed significant differences for serial seven subtest scores between DAT and persistent MCI (P<0.05). Rates of change in subtests of orientation and memory and total MMSE scores predicted DAT (P<0.01). Decreasing orientation and total MMSE scores predicted VaD conversion rates of MCI to DAT at 2 years were 20.06% among single-domain MCI versus 41.7% for multi-domain MCI (P<0.05). Subjects with MCI often have impaired cognitive domains other than memory and show rapid deterioration, which predicts DAT. VaD sometimes mimics DAT with subtle cognitive impairment appearing before onset of dementia.

Keywords:  Alzheimer disease, Memory loss, Cognitive disorders, Dementia, vascular, Diagnosis, Psychometrics, Risk factors, Mild cognitive impairment, Cognitive screening

Abbreviations:  AACD, age-associated cognitive decline, AAMI, age-associated memory impairment, AAN, American Academy of Neurology, ADRDA, Alzheimer Disease and Related Disorders Association, AIRENS, Association Internationale pour la Recherche et l'Enseignement en Neurosciences, CCSE, Cognitive Capacity Screening Examination, CIND, cognitive impairment no dementia, CT, computed tomography, DAT, dementia of Alzheimer's type, EEG, electroencephalogram, EKG, electrocardiogram, HDRS, Hamilton Depression Rating Scale, MCI, mild cognitive impairment, MMSE, Mini-Mental State Examination, MRI, magnetic resonance imaging, NINCDS, National Institute of Neurological and Communicative Disorders and Stroke, NTR, neurotrophin receptor, VaD, vascular dementia, VCI, vascular cognitive impairment, WHO, World Health Organization

To access this article, please choose from the options below

Login to an existing account or Register a new account.

  • Purchase this article for 31.50 USD (You must login/register to purchase this article)

    Online access for 24 hours. The PDF version can be downloaded as your permanent record.

  • Subscribe to this title

    Get unlimited online access to this article and all other articles in this title 24/7 for one year.

  • Claim access now

    For current subscribers with Society Membership or Account Number.

  • Visit SciVerse ScienceDirect to see if you have access via your institution.
 

PII: S0022-510X(02)00159-4

Journal of the Neurological Sciences
Volume 201, Issue 1 , Pages 19-25, 15 September 2002