Cognitive frailty and falls in Chinese elderly people: a population-based longitudinal study.

Abstract:

BACKGROUND AND PURPOSE:Falling is considered an important public health problem among older people. A recent cross-sectional study suggested that cognitive frailty (CF) is associated with falls. We aimed to explore whether CF is a risk factor for falls in a population-based longitudinal study. METHODS:Using data from the Rugao Longevity and Aging Study, physical frailty was assessed according to the modified Fried's phenotype, and the 20% of participants with the lowest scores on the Revised Hasegawa Dementia Scale were defined as having cognitive impairment (CoI). Cognitive frailty (CF) was defined as the coexistence of physical frailty and CoI, but excluded severe CoI (revised Hasegawa Dementia Scale score ≤ 10). The outcome of number of falls in the previous 12 months was measured using a questionnaire. RESULTS:At baseline, the prevalence of CF was 2.6% and the prevalence of two or more falls was 6.7%. Cross-sectional analysis found that two or more falls was associated with physical frailty without CoI (odds ratio [OR] 6.79, 95% confidence interval [CI] 3.17-14.56), pre-frailty with CoI (OR 4.54, 95% CI 2.44-8.44) and CF (OR 3.51, 95% CI 1.18-10.44). Slow gait with CoI was associated with two or more falls (OR 2.21, 95% CI 1.08-4.53). At 3-year follow-up, the prevalence of two or more falls was 10.6%. Logistic regression analysis showed that, compared with the robust and non-CoI elderly groups, the CF elderly group had a higher risk of two or more falls (OR 3.41, 95% CI 1.11-10.50). CONCLUSIONS:Cognitive frailty was associated with two or more falls at baseline and might be a risk factor for two or more falls after 3 years. Early screening of CF might be beneficial in the prevention of falls.

journal_name

Eur J Neurol

authors

Ma Y,Li X,Pan Y,Zhao R,Wang X,Jiang X,Li S

doi

10.1111/ene.14572

subject

Has Abstract

pub_date

2021-02-01 00:00:00

pages

381-388

issue

2

eissn

1351-5101

issn

1468-1331

journal_volume

28

pub_type

杂志文章
  • Practice recommendations for neurovascular ultrasound investigations of acute stroke patients in the setting of the COVID-19 pandemic: an expert consensus from the European Society of Neurosonology and Cerebral Hemodynamics.

    abstract:BACKGROUND AND PURPOSE:Patients with acute ischemic stroke are at high-risk for contracting COVID-19 infection. Additionally, healthcare professionals including neurovascular ultrasound providers are also at risk of being infected by SARS-CoV-2 virus. Yet, preparedness to continue to guarantee hyperacute treatment is v...

    journal_title:European journal of neurology

    pub_type: 杂志文章,实务指引

    doi:10.1111/ene.14334

    authors: Baracchini C,Pieroni A,Kneihsl M,Azevedo E,Diomedi M,Pascazio L,Wojczal J,Lucas C,Bartels E,Bornstein NM,Csiba L,Valdueza J,Tsivgoulis G,Malojcic B

    更新日期:2020-09-01 00:00:00

  • Long-term efficacy and safety of erenumab in migraine prevention: Results from a 5-year, open-label treatment phase of a randomized clinical trial.

    abstract:BACKGROUND AND PURPOSE:Although erenumab has demonstrated significant reduction in migraine frequency and improved quality of life in studies lasting 3 to 12 months, little is known about long-term therapy. METHODS:This study was an open-label, 5-year treatment phase following a 12-week, double-blind, placebo-controll...

    journal_title:European journal of neurology

    pub_type: 杂志文章

    doi:10.1111/ene.14715

    authors: Ashina M,Goadsby PJ,Reuter U,Silberstein S,Dodick DW,Xue F,Zhang F,Paiva da Silva Lima G,Cheng S,Mikol DD

    更新日期:2021-01-05 00:00:00

  • Transient ischemic attack without self-awareness of symptoms witnessed by bystanders: analysis of the PROMISE-TIA registry.

    abstract:BACKGROUND AND PURPOSE:A transient ischemic attack (TIA) can occur without self-awareness of symptoms. We aimed to investigate characteristics of patients with a tissue-based diagnosis of TIA but having no self-awareness of their symptoms and whose symptoms were witnessed by bystanders. METHODS:We used data from the m...

    journal_title:European journal of neurology

    pub_type: 杂志文章

    doi:10.1111/ene.14550

    authors: Tanaka K,Uehara T,Ohara T,Sato S,Hayakawa M,Kimura K,Okada Y,Hasegawa Y,Tanahashi N,Suzuki A,Nakagawara J,Arii K,Nagahiro S,Ogasawara K,Uchiyama S,Matsumoto M,Iihara K,Toyoda K,Minematsu K,PROMISE-TIA study Investig

    更新日期:2021-02-01 00:00:00

  • Seven novel mutations and four exon deletions in a collection of Norwegian patients with SPG4 hereditary spastic paraplegia.

    abstract::To establish the phenotypic variation and frequency of SPAST mutations or deletions in Norwegian patients with hereditary spastic paraplegia (HSP), we examined 59 unrelated patients with HSP and screened for DNA point mutations and microdeletions in SPG4. Forty-one had a familial history, 35 had a clear dominant inher...

    journal_title:European journal of neurology

    pub_type: 杂志文章

    doi:10.1111/j.1468-1331.2007.01861.x

    authors: Erichsen AK,Inderhaug E,Mattingsdal M,Eiklid K,Tallaksen CM

    更新日期:2007-07-01 00:00:00

  • Charcot-Marie-Tooth type X: unusual phenotype of a novel CX32 mutation.

    abstract:BACKGROUND:X-linked Charcot-Marie-Tooth disease (CMTX), caused by mutations in the gene encoding connexin32, is the second most common form of inherited demyelinating neuropathy, next to CMT 1A, and accounts for 10-20% of all hereditary demyelinating neuropathies. AIMS OF THE STUDY:To describe clinical and electrophys...

    journal_title:European journal of neurology

    pub_type: 杂志文章

    doi:10.1111/j.1468-1331.2008.02263.x

    authors: Mazzeo A,Di Leo R,Toscano A,Muglia M,Patitucci A,Messina C,Vita G

    更新日期:2008-10-01 00:00:00

  • A common leucine-rich repeat kinase 2 gene mutation in familial and sporadic Parkinson's disease in Russia.

    abstract::A PARK8 form of Parkinson's disease (PD) is caused by a novel gene, leucine-rich repeat kinase 2 (LRRK2), and a single mutation G2019S was found in a proportion of LRRK2-associated cases of diverse ethnic origins. We performed the LRRK2 G2019S mutation analysis in 304 Russian patients with PD, including 291 sporadic a...

    journal_title:European journal of neurology

    pub_type: 杂志文章

    doi:10.1111/j.1468-1331.2007.01685.x

    authors: Illarioshkin SN,Shadrina MI,Slominsky PA,Bespalova EV,Zagorovskaya TB,Bagyeva GKh,Markova ED,Limborska SA,Ivanova-Smolenskaya IA

    更新日期:2007-04-01 00:00:00

  • Mini-Mental State Examination: a normative study in Italian elderly population.

    abstract::The Mini-Mental State Examination (MMSE), a brief test to assess cognitive status, is heavily influenced by age and education. It was administered to 1019 elderly subjects (aged 65-89 years) living in three different Italian cities. A statistical non-linear regression model was built up in order to obtain adjustment c...

    journal_title:European journal of neurology

    pub_type: 杂志文章

    doi:10.1111/j.1468-1331.1996.tb00423.x

    authors: Magni E,Binetti G,Bianchetti A,Rozzini R,Trabucchi M

    更新日期:1996-05-01 00:00:00

  • Stroke following internal carotid artery occlusion - a contra-indication for intravenous thrombolysis?

    abstract::Between March 1996 and December 1997, 15 consecutive patients with carotid artery occlusion diagnosed with duplex sonography were treated with intravenous recombinant tissue plasminogen activator (rt-PA), following a protocol similar to that of the National Institute of Neurological Disorders and Stroke (NINDS) study....

    journal_title:European journal of neurology

    pub_type: 杂志文章

    doi:10.1046/j.1468-1331.1999.610051.x

    authors: Rudolf J,Neveling M,Grond M,Schmulling S,Stenzel C,Heiss WD

    更新日期:1999-01-01 00:00:00

  • Guidelines for treatment of autoimmune neuromuscular transmission disorders.

    abstract:BACKGROUND:Important progress has been made in our understanding of the autoimmune neuromuscular transmission (NMT) disorders; myasthenia gravis (MG), Lambert-Eaton myasthenic syndrome (LEMS) and neuromyotonia (Isaacs' syndrome). METHODS:To prepare consensus guidelines for the treatment of the autoimmune NMT disorders...

    journal_title:European journal of neurology

    pub_type: 杂志文章,实务指引

    doi:10.1111/j.1468-1331.2010.03019.x

    authors: Skeie GO,Apostolski S,Evoli A,Gilhus NE,Illa I,Harms L,Hilton-Jones D,Melms A,Verschuuren J,Horge HW,European Federation of Neurological Societies.

    更新日期:2010-07-01 00:00:00

  • Evolving atherosclerosis at carotid and intracranial arteries in Japanese patients with ischemic heart disease: a 5-year longitudinal study with MR angiography.

    abstract::Progression of atherosclerosis at extracranial carotid and intracranial arteries in patients with ischemic heart disease (IHD) is not well defined. We carried out a 5-year longitudinal study with magnetic resonance angiography (MRA) of patients with IHD to assess the incidence of progression of atherosclerosis at extr...

    journal_title:European journal of neurology

    pub_type: 杂志文章

    doi:10.1046/j.1468-1331.2003.00620.x

    authors: Uehara T,Tabuchi M,Mori E,Yamadori A

    更新日期:2003-09-01 00:00:00

  • Advanced multiparametric magnetic resonance imaging of multinodular and vacuolating neuronal tumor.

    abstract:BACKGROUND AND PURPOSE:Multinodular and vacuolating neuronal tumor (MVNT) of the cerebrum is a rare brain lesion with suggestive imaging features. The aim of our study was to report the largest series of MVNTs so far and to evaluate the utility of advanced multiparametric magnetic resonance (MR) techniques. METHODS:Th...

    journal_title:European journal of neurology

    pub_type: 杂志文章

    doi:10.1111/ene.14264

    authors: Lecler A,Broquet V,Bailleux J,Carsin B,Adle-Biassette H,Baloglu S,Forestier G,Bonneville F,Calvier E,Chauvet D,Comby PO,Cottier JP,Cotton F,Deschamps R,Diard-Detoeuf C,Ducray F,Drissi C,Elmaleh M,Farras J,Aguilar Ga

    更新日期:2020-08-01 00:00:00

  • Clinical and molecular analysis of 11 Sicilian SCA2 families: influence of gender on age at onset.

    abstract::Autosomal dominant cerebellar ataxias (ADCAs) are a complex group of slowly progressive neurodegenerative disorders characterized by gait and stance ataxia, dysarthria and other symptoms of nervous system involvement. ADCA type I is the commonest form and is genetically heterogeneous; several loci have been identified...

    journal_title:European journal of neurology

    pub_type: 杂志文章

    doi:10.1046/j.1468-1331.1999.630301.x

    authors: Giuffrida S,Lanza S,Restivo DA,Saponara R,Valvo SC,Le Pira F,Trovato Salinaro A,Spinella F,Nicoletti A,Condorelli DF

    更新日期:1999-05-01 00:00:00

  • T-cell interleukin-6 receptor binding in interferon-beta-1b-treated multiple sclerosis patients.

    abstract::Multiple sclerosis (MS) is a T-cell-mediated autoimmune demyelinating disease of the central nervous system, associated with an altered cytokine network. We previously assayed peripheral blood T-lymphocyte binding for two prototypic cytokines, tumour necrosis factor-alpha (TNF-alpha) and interleukin-6 (IL-6), and foun...

    journal_title:European journal of neurology

    pub_type: 杂志文章

    doi:10.1046/j.1468-1331.2000.00139.x

    authors: Bongioanni P,Lombardo F,Moscato G,Mosti S,Meucci G

    更新日期:2000-11-01 00:00:00

  • Subacute rhombencephalitis optica responsive to intravenous immunoglobulins.

    abstract::A 53-year-old man presented with optic neuritis, followed within 10 weeks by a subacute progression of weakness, ataxia, and multiple cranial nerve palsies. Cranial magnetic resonance imaging demonstrated multiple T2-hyperintense lesions extending from the ponto-medullary junction to the thalamus and internal capsule....

    journal_title:European journal of neurology

    pub_type: 杂志文章

    doi:10.1046/j.1468-1331.2003.00543.x

    authors: Zivković SA,Heyman R,Pless M

    更新日期:2003-01-01 00:00:00

  • Migraine, allodynia, and implications for treatment.

    abstract::Allodynia--perception of pain from non-noxious stimuli--is a common clinical feature in various pain syndromes. The significance for migraine has increasingly been recognized and the pathophysiology has been investigated in detail. Allodynia is a marker for sensitization of central trigeminal neurons. Intensity and pe...

    journal_title:European journal of neurology

    pub_type: 杂志文章,评审

    doi:10.1111/j.1468-1331.2008.02343.x

    authors: Schürks M,Diener HC

    更新日期:2008-12-01 00:00:00

  • Prescribing patterns of antiepileptic drugs in Italy: a nationwide population-based study in the years 2000-2005.

    abstract::To evaluate prevalence of use and prescribing patterns of antiepileptic drugs (AEDs) in Italian general practice. Primary care data were obtained from the Health Search Database, a longitudinal observational database implemented by the Italian College of General Practitioners (GPs). We selected 465 061 subjects regist...

    journal_title:European journal of neurology

    pub_type: 杂志文章

    doi:10.1111/j.1468-1331.2007.01970.x

    authors: Savica R,Beghi E,Mazzaglia G,Innocenti F,Brignoli O,Cricelli C,Caputi AP,Musolino R,Spina E,Trifirò G

    更新日期:2007-12-01 00:00:00

  • Subthreshold depression and subjective cognitive complaints in Parkinson's disease.

    abstract:BACKGROUND AND PURPOSE:Subthreshold depression (SubD) is characterized by clinically relevant depressive symptoms not meeting criteria for major depression. The possible association of SubD with subjective cognitive complaints and/or objective cognitive impairments was investigated in a sample of consecutive, non-demen...

    journal_title:European journal of neurology

    pub_type: 杂志文章

    doi:10.1111/ene.12219

    authors: Santangelo G,Vitale C,Trojano L,Angrisano MG,Picillo M,Errico D,Agosti V,Grossi D,Barone P

    更新日期:2014-03-01 00:00:00

  • Prodrome in relapsing-remitting and primary progressive multiple sclerosis.

    abstract:BACKGROUND AND PURPOSE:The multiple sclerosis prodrome remains poorly understood. We aimed to examine the prodrome in people with relapsing remitting multiple sclerosis at onset (RMS) and primary progressive multiple sclerosis (PPMS). METHODS:We conducted a matched cohort study using clinical and linked health adminis...

    journal_title:European journal of neurology

    pub_type: 杂志文章

    doi:10.1111/ene.13925

    authors: Wijnands JMA,Zhu F,Kingwell E,Zhao Y,Evans C,Fisk JD,Marrie RA,Tremlett H

    更新日期:2019-07-01 00:00:00

  • Neurology residency training in Europe--the current situation.

    abstract:INTRODUCTION:Little is known about neurological training curricula in Europe. A joint approach by the European Federation of Neurological Societies (EFNS), the Union of European Medical Specialists/European Board of Neurology and the European Association of Young Neurologist and Trainees was established to explore the ...

    journal_title:European journal of neurology

    pub_type: 杂志文章

    doi:10.1111/j.1468-1331.2010.03219.x

    authors: Struhal W,Sellner J,Lisnic V,Vécsei L,Müller E,Grisold W

    更新日期:2011-04-01 00:00:00

  • Comparative evaluation of 2D time-of-flight and 3D elliptic centric contrast-enhanced MR venography in patients with presumptive cerebral venous and sinus thrombosis.

    abstract::We retrospectively evaluated an elliptic centric ordered 3D (ec 3D) magnetic resonance venography (MRV) technique in comparison to 2D time-of-flight (2D TOF) MRV in patients with presumptive cerebral venous sinus thrombosis (CVST). Twenty-five patients (mean age 40.6 +/- 16.5 years) with presumptive CVST underwent cer...

    journal_title:European journal of neurology

    pub_type: 杂志文章

    doi:10.1111/j.1468-1331.2006.01574.x

    authors: Klingebiel R,Bauknecht HC,Bohner G,Kirsch R,Berger J,Masuhr F

    更新日期:2007-02-01 00:00:00

  • Decreased serum selenium concentrations in patients with Parkinson's disease.

    abstract::Selenium is an essential component of the antioxidant enzyme glutathione peroxidase. The activity of this enzyme is reduced in the substantia nigra of patients with Parkinson's disease (PD), but the results of studies on erythrocytes are controversial. We compared the serum levels of selenium and the 24 h urinary sele...

    journal_title:European journal of neurology

    pub_type: 杂志文章

    doi:10.1111/j.1468-1331.1995.tb00102.x

    authors: Jiménez-Jiménez FJ,Molina JA,Arrieta FJ,Aguilar MV,Cabrera-Valdivia F,Vázquez A,Jorge-Santamaría A,Seijas V,Fernández-Calle P,Martínez-Para MC

    更新日期:1995-04-01 00:00:00

  • EFNS guidelines on the molecular diagnosis of neurogenetic disorders: general issues, Huntington's disease, Parkinson's disease and dystonias.

    abstract:BACKGROUND AND PURPOSE:These EFNS guidelines on the molecular diagnosis of neurogenetic disorders are designed to provide practical help for the general neurologist to make appropriate use of molecular genetics in diagnosing neurogenetic disorders. Since the publication of the first two EFNS-guideline papers on the mol...

    journal_title:European journal of neurology

    pub_type: 杂志文章

    doi:10.1111/j.1468-1331.2009.02646.x

    authors: Harbo HF,Finsterer J,Baets J,Van Broeckhoven C,Di Donato S,Fontaine B,De Jonghe P,Lossos A,Lynch T,Mariotti C,Schöls L,Spinazzola A,Szolnoki Z,Tabrizi SJ,Tallaksen C,Zeviani M,Burgunder JM,Gasser T,EFNS.

    更新日期:2009-07-01 00:00:00

  • Electrophysiological assessment of visual function in patients with non-arteritic ischaemic optic neuropathy.

    abstract:BACKGROUND AND PURPOSE:Our study aims to evaluate retinal function and neural conduction in post-retinal visual pathways of patients with non-arteritic ischaemic optic neuropathy (NION). METHODS:Twenty patients (mean age: 63.7 +/- 5.96 year) with NION and 20 age-similar control subjects were enrolled. Simultaneous rec...

    journal_title:European journal of neurology

    pub_type: 杂志文章

    doi:10.1111/j.1468-1331.2008.02200.x

    authors: Parisi V,Gallinaro G,Ziccardi L,Coppola G

    更新日期:2008-08-01 00:00:00

  • Histamine-N-methyl transferase polymorphism and risk for multiple sclerosis.

    abstract:BACKGROUND:Histamine N-methyltransferase (HNMT) is the main metabolizing enzyme of histamine (a mediator of inflammation implicated in the pathogenesis of multiple sclerosis-MS) in the CNS. We have investigated the possible association between a single nucleotide polymorphism of the HNMT (chromosome 2q22.1), that cause...

    journal_title:European journal of neurology

    pub_type: 杂志文章

    doi:10.1111/j.1468-1331.2009.02720.x

    authors: García-Martín E,Martínez C,Benito-León J,Calleja P,Díaz-Sánchez M,Pisa D,Alonso-Navarro H,Ayuso-Peralta L,Torrecilla D,Agúndez JA,Jiménez-Jiménez FJ

    更新日期:2010-02-01 00:00:00

  • The neuropsychiatric phenotype in CACNA1A mutations: a retrospective single center study and review of the literature.

    abstract:BACKGROUND AND PURPOSE:CACNA1A encodes the α1 subunit of the neuronal calcium channel P/Q. CACNA1A mutations underlie three allelic disorders: familial hemiplegic migraine type 1 (FHM1), episodic ataxia type 2 (EA2) and spinocerebellar ataxia type 6 (SCA6). A clear-cut genotype-phenotype correlation is often lacking si...

    journal_title:European journal of neurology

    pub_type: 杂志文章

    doi:10.1111/ene.13765

    authors: Indelicato E,Nachbauer W,Karner E,Eigentler A,Wagner M,Unterberger I,Poewe W,Delazer M,Boesch S

    更新日期:2019-01-01 00:00:00

  • Risk factors for chronic inflammatory demyelinating polyradiculoneuropathy (CIDP): antecedent events, lifestyle and dietary habits. Data from the Italian CIDP Database.

    abstract:BACKGROUND AND PURPOSE:The role of lifestyle and dietary habits and antecedent events has not been clearly identified in chronic inflammatory demyelinating polyradiculoneuropathy (CIDP). METHODS:Information was collected about modifiable environmental factors and antecedent infections and vaccinations in patients with...

    journal_title:European journal of neurology

    pub_type: 杂志文章

    doi:10.1111/ene.14044

    authors: Doneddu PE,Bianchi E,Cocito D,Manganelli F,Fazio R,Filosto M,Mazzeo A,Cosentino G,Cortese A,Jann S,Clerici AM,Antonini G,Siciliano G,Luigetti M,Marfia GA,Briani C,Lauria G,Rosso T,Cavaletti G,Carpo M,Benedetti L,

    更新日期:2020-01-01 00:00:00

  • Association between carotid stenosis or lacunar infarction and incident dementia in patients with vascular risk factors.

    abstract:BACKGROUND AND PURPOSE:The association between vascular risk factors and dementia is of interest. Several studies have shown that cerebral small vessel disease (SVD) is associated with dementia. However, the association between cerebral large vessel disease (LVD) and dementia has not been thoroughly examined. METHODS:...

    journal_title:European journal of neurology

    pub_type: 杂志文章

    doi:10.1111/ene.12553

    authors: Kitagawa K,Miwa K,Yagita Y,Okazaki S,Sakaguchi M,Mochizuki H

    更新日期:2015-01-01 00:00:00

  • Evolution of striatal degeneration in McLeod syndrome.

    abstract:BACKGROUND AND PURPOSE:McLeod neuroacanthocytosis syndrome (MLS) is an X-linked multisystem disorder with CNS manifestations resembling Huntington disease. Neuroimaging studies revealed striatal atrophy with predominance of the caudate nucleus. Our previous cross-sectional MRI study showed an association of volume loss...

    journal_title:European journal of neurology

    pub_type: 杂志文章

    doi:10.1111/j.1468-1331.2009.02872.x

    authors: Valko PO,Hänggi J,Meyer M,Jung HH

    更新日期:2010-04-01 00:00:00

  • White matter microstructural changes in pure Alzheimer's disease and subcortical vascular dementia.

    abstract:BACKGROUND AND PURPOSE:Recent studies have demonstrated that Alzheimer's disease (AD) and subcortical vascular dementia (SVaD) have white matter (WM) microstructural changes. However, previous studies on AD and SVaD rarely eliminated the confounding effects of patients with mixed Alzheimer's and cerebrovascular disease...

    journal_title:European journal of neurology

    pub_type: 杂志文章

    doi:10.1111/ene.12645

    authors: Kim YJ,Kwon HK,Lee JM,Kim YJ,Kim HJ,Jung NY,Kim ST,Lee KH,Na DL,Seo SW

    更新日期:2015-04-01 00:00:00

  • A putative polymorphic Val44Ala variation in the synphilin-1 gene is undetectable in Japanese sporadic Parkinson's disease patients.

    abstract::Recently, a novel protein-interaction partner of alpha-synuclein, designated synphilin-1, is identified as a constituent of Lewy bodies (LB) in Parkinson's disease (PD) brains. To investigate an involvement of genetic variations of synphilin-1 in development of sporadic PD, a possible single nucleotide polymorphism (S...

    journal_title:European journal of neurology

    pub_type: 临床试验,杂志文章

    doi:10.1046/j.1468-1331.2002.00333.x

    authors: Satoh JI,Kuroda Y

    更新日期:2002-01-01 00:00:00