Neurological abnormalities predict disability: the LADIS (Leukoaraiosis And DISability) study
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  • 作者:Anna Poggesi (1)
    Alida Gouw (2)
    Wiesje van der Flier (2)
    Giovanni Pracucci (1)
    Hugues Chabriat (3)
    Timo Erkinjuntti (4)
    Franz Fazekas (5)
    José M. Ferro (6)
    Christian Blahak (7)
    Peter Langhorne (8)
    John O’Brien (9)
    Reinhold Schmidt (5)
    Marieke C. Visser (2)
    Lars-Olof Wahlund (10)
    Gunhild Waldemar (11)
    Anders Wallin (12)
    Philip Scheltens (2)
    Domenico Inzitari (1)
    Leonardo Pantoni (13)
  • 关键词:White matter changes ; Disability ; Cerebrovascular diseases ; Neurological examination ; MRI
  • 刊名:Journal of Neurology
  • 出版年:2014
  • 出版时间:June 2014
  • 年:2014
  • 卷:261
  • 期:6
  • 页码:1160-1169
  • 全文大小:
  • 参考文献:1. Inzitari M, Pozzi C, Ferrucci L et al (2008) Subtle neurological abnormalities as risk factors for cognitive and functional decline, cerebrovascular events, and mortality in older community-dwelling adults. Arch Intern Med 168(12):1270-276 CrossRef
    2. Román GC, Erkinjuntti T, Wallin A, Pantoni L, Chui HE (2002) Subcortical ischaemic vascular dementia. Lancet Neurol 1(7):426-36 CrossRef
    3. Pantoni L, Garcia JH (1995) The significance of cerebral white matter abnormalities 100?years after Binswanger’s report. Rev Stroke 26(7):1293-301 CrossRef
    4. Pantoni L (2010) Cerebral small vessel disease: from pathogenesis and clinical characteristics to therapeutic challenges. Lancet Neurol 9(7):689-01 CrossRef
    5. Bernick C, Kuller L, Dulberg C et al (2001) Silent MRI infarcts and the risk of future stroke: the cardiovascular health study. Neurology 57(7):1222-229 CrossRef
    6. Vermeer SE, Hollander M, van Dijk EJ, Hofman A, Koudstaal PJ, Breteler MMB (2003) Silent brain infarcts and white-matter lesions increase stroke risk in the general population: the Rotterdam scan study. Stroke 34(5):1126-129 CrossRef
    7. Vermeer SE, Prins ND, den Heijer T, Hofman A, Koudstaal PJ, Breteler MM (2003) Silent brain infarcts and the risk of dementia and cognitive decline. N Engl J Med 348(13):1215-222 CrossRef
    8. Breteler MMB, Van Swieten JC, Bots ML et al (1994) Cerebral white matter lesions, vascular risk factors, and cognitive function in a population-based study: the Rotterdam study. Neurology 44(7):1246-252 CrossRef
    9. Prins ND, van Dijk EJ, den Heijer T et al (2004) Cerebral white matter lesions and the risk of dementia. Arch Neurol 61(10):1531-534 CrossRef
    10. Prins ND, van Dijk EJ, den Heijer T et al (2005) Cerebral small-vessel disease and decline in information processing speed, executive function and memory. Brain 128(Pt9):2034-041 CrossRef
    11. Baezner H, Blahak C, Poggesi A, LADIS Study Group et al (2008) Association of gait and balance disorders with age-related white matter changes: the LADIS study. Neurology 70(12):935-42 CrossRef
    12. Rosano C, Kuller LH, Chung H, Arnold AM, Longstreth WT Jr, Newman AB (2005) Subclinical brain magnetic resonance imaging abnormalities predict physical functional decline in high-functioning older adults. J Am Geriatr Soc 53(4):649-54 CrossRef
    13. Iseki K, Hanakawa T, Hashikawa K et al (2010) Gait disturbance associated with white matter changes: a gait analysis and blood flow study. Neuroimage 49(2):1659-666 CrossRef
    14. de Groot JC, de Leeuw F-E, Oudkerk M et al (2000) Cerebral white matter lesions and depressive symptoms in elderly adults. Arch Gen Psychiatry 57(11):1071-076 CrossRef
    15. Jorm AF, Anstey KJ, Christensen H et al (2005) MRI hyperintensities and depressive symptoms in a community sample of individuals 60-4?years old. Am J Psychiatry 162(4):699-05 CrossRef
    16. Teodorczuk A, O’Brien JT, Firbank MJ et al (2007) LADIS Group. White matter changes and late-life depressive symptoms: longitudinal study. Br J Psychiatry 191:212-17 CrossRef
    17. Sakakibara R, Hattori T, Uchiyama T, Yamanishi T (1999) Urinary function in elderly people with and without leukoaraiosis: relation to cognitive and gait function. J Neurol Neurosurg Psychiatry 67(5):658-60 CrossRef
    18. Poggesi A, Pracucci G, Chabriat H, Leukoaraiosis And DISability Study Group et al (2008) Urinary complaints in nondisabled elderly people with age-related white matter changes: the Leukoaraiosis And DISability (LADIS) Study. J Am Geriatr Soc 56(9):1638-643 CrossRef
    19. Inzitari D, Simoni M, Pracucci G, LADIS Study Group et al (2007) Risk of rapid global functional decline in elderly patients with severe cerebral age-related white matter changes: the LADIS study. Arch Intern Med 167(1):81-8 CrossRef
    20. Inzitari D, Pracucci G, Poggesi A, LADIS Study Group et al (2009) Changes in white matter as determinant of global functional decline in older independent outpatients: three year follow-up of LADIS (leukoaraiosis and disability) study cohort. BMJ 339:b2477. doi:10.1136/bmj.b2477 CrossRef
    21. Poggesi A, Gouw A, van der Flier W et al (2013) Cerebral white matter changes are associated with abnormalities on neurological examination in non-disabled elderly: the LADIS study. J Neurol 260(4):1014-021 CrossRef
    22. Pantoni L, Basile AM, Pracucci G et al (2005) Impact of age-related cerebral white matter changes on the transition to disability—the LADIS study: rationale, design and methodology. Neuroepidemiology 24(1-):51-2 CrossRef
    23. Fazekas F, Chawluk JB, Alavi A, Hurtig HI, Zimmerman RA (1987) MR Signal Abnormalities at 1.5 T in alzheimer’s dementia and normal aging. AJR Am J Roentgenol 149(2):351-56 CrossRef
    24. Ryberg C, Rostrup E, Sj?strand K et al (2008) White matter changes contribute to corpus callosum atrophy in the elderly: the LADIS study. AJNR Am J Neuroradiol 29(8):1498-504 CrossRef
    25. Lawton MP, Brody EM (1969) Assessment of older people: self-maintaining and instrumental activities of daily living. Gerontologist 9(3):179-86 CrossRef
    26. American Psychiatric Association (1994) Diagnostic and statistical manual of mental disorders, fourth edition (DSM-IV). American Psychiatric Association, Washington (DC)
    27. Hatano S (1976) Experience from a multicentre stroke register: a preliminary report. Bull WHO 54(5):541-53
    28. Prakash C, Stern G (1973) Neurological signs in the elderly. Age Ageing 2(1):24-7 CrossRef
    29. Schut LJ (1998) Motor system changes in the aging brain: what is normal and what is not. Geriatrics 53(Suppl 1):S16–S19
    30. Yamanouchi H, Nagura H (1997) Neurological signs and frontal white matter lesions in vascular parkinsonism. A clinicopathologic study. Stroke 28(5):965-69 CrossRef
    31. Benamer HT, Grosset DG (2009) Vascular parkinsonism: a clinical review. Eur Neurol 61(1):11-5 CrossRef
    32. Staekenborg SS, van der Flier WM, van Straaten EC, Lane R, Barkhof F, Scheltens P (2008) Neurological signs in relation to type of cerebrovascular disease in vascular dementia. Stroke 39(2):317-22 CrossRef
    33. Boustani M, Justiss MD (2008) Subtle neurological abnormalities and functional cognition in older adults. Arch Intern Med 168(12):1252-253 CrossRef
  • 作者单位:Anna Poggesi (1)
    Alida Gouw (2)
    Wiesje van der Flier (2)
    Giovanni Pracucci (1)
    Hugues Chabriat (3)
    Timo Erkinjuntti (4)
    Franz Fazekas (5)
    José M. Ferro (6)
    Christian Blahak (7)
    Peter Langhorne (8)
    John O’Brien (9)
    Reinhold Schmidt (5)
    Marieke C. Visser (2)
    Lars-Olof Wahlund (10)
    Gunhild Waldemar (11)
    Anders Wallin (12)
    Philip Scheltens (2)
    Domenico Inzitari (1)
    Leonardo Pantoni (13)

    1. Neuroscience Section, NEUROFARBA Department, University of Florence, Florence, Italy
    2. Department of Radiology and Neurology, VU Medical Centre, Amsterdam, The Netherlands
    3. Department of Neurology, Hopital Lariboisiere, Paris, France
    4. Memory Research Unit, Department of Clinical Neurosciences, Helsinki University, Helsinki, Finland
    5. Department of Neurology, Medical University, Graz, Austria
    6. Servi?o de Neurologia, Centro de Estudos Egas Moniz, Hospital de Santa Maria Lisboa, Lisbon, Portugal
    7. Department of Neurology, Universitaets Medizin Mannheim, University of Heidelberg, Mannheim, Germany
    8. Academic Department for Geriatric Medicine, Glasgow Royal Infirmary, Glasgow, UK
    9. Institute for Ageing and Health, University of Newcastle, Newcastle upon Tyne, UK
    10. Department of Clinical Neuroscience and Family Medicine, Karolinska Institute, Huddinge University Hospital, Huddinge, Sweden
    11. Department of Neurology, Memory Disorders Research Unit, Copenhagen University Hospital, Copenhagen, Denmark
    12. Institute of Clinical Neuroscience, Goteborg University, G?teborg, Sweden
    13. Stroke Unit and Neurology, Azienda Ospedaliero Universitaria Careggi, Largo Brambilla 3, 50134, Florence, Italy
  • ISSN:1432-1459
文摘
To investigate the role of neurological abnormalities and magnetic resonance imaging (MRI) lesions in predicting global functional decline in a cohort of initially independent-living elderly subjects. The Leukoaraiosis And DISability (LADIS) Study, involving 11 European centres, was primarily aimed at evaluating age-related white matter changes (ARWMC) as an independent predictor of the transition to disability (according to Instrumental Activities of Daily Living scale) or death in independent elderly subjects that were followed up for 3?years. At baseline, a standardized neurological examination was performed. MRI assessment included age-related white matter changes (ARWMC) grading (mild, moderate, severe according to the Fazekas-scale), count of lacunar and non-lacunar infarcts, and global atrophy rating. Of the 633 (out of the 639 enrolled) patients with follow-up information (mean age 74.1?±?5.0?years, 45?% males), 327 (51.7?%) presented at the initial visit with ? neurological abnormality and 242 (38?%) reached the main study outcome. Cox regression analyses, adjusting for MRI features and other determinants of functional decline, showed that the baseline presence of any neurological abnormality independently predicted transition to disability or death [HR (95?% CI) 1.53 (1.01-.34)]. The hazard increased with increasing number of abnormalities. Among MRI lesions, only ARWMC of severe grade independently predicted disability or death [HR (95?% CI) 2.18 (1.37-.48)]. In our cohort, presence and number of neurological examination abnormalities predicted global functional decline independent of MRI lesions typical of the aging brain and other determinants of disability in the elderly. Systematically checking for neurological examination abnormalities in older patients may be cost-effective in identifying those at risk of functional decline.

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