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      KCI등재후보

      알츠하이머병 및 피질하허혈성혈관치매 환자들의 국소 뇌 부피 정량 비교 = Comparison of Regional Brain Volume of Alzheimer’s Disease and Subcortical Ischemic Vascular Dementia

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      https://www.riss.kr/link?id=A103915571

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      다국어 초록 (Multilingual Abstract)

      Background: The findings like the brain atrophy and ventricular dilatation can be also shown on magnetic resonance imaging (MRI) of the patients with subcortical ischemic vascular dementia (SIVD) as well as Alzheimer’s disease (AD), and some patient...

      Background: The findings like the brain atrophy and ventricular dilatation can be also shown on
      magnetic resonance imaging (MRI) of the patients with subcortical ischemic vascular dementia
      (SIVD) as well as Alzheimer’s disease (AD), and some patients with SIVD have the pathology of
      AD. There have been also objected to that SIVD is not the true vascular dementia (VaD), but the
      mixed type with AD. We compared the regional volumes of the gray and white matters between
      AD and SIVD with the hypothesis that the brain atrophy of the patients with SIVD shown on MRI
      is a relative result from the atrophy of the white matter, not from the atrophy of the gray matter.
      Methods: Twelve AD patients and 13 SIVD patients were included in this study. Eleven controls
      without the cognitive impairment were also included. The volumes of the bilateral frontal, temporal,
      parietal areas, and the bilateral hippocampus and entorhinal cortex were obtained. After the correction
      with the ratio to the intracranial volume, the regional volumes were compared among AD,
      SIVD and the controls by analysis of variances with multiple comparisons. Results: Whole brain
      volume of the patients with AD was the smallest (p=0.042). The ventricular volumes of the patients
      with AD and SIVD were smaller than that of the controls (p=0.001). For the volumes of frontal, temporal
      and parietal regions were not different. The volumes of the bilateral hippocampus (p=0.009)
      and entorhinal cortex (p=0.002 in the right side and p=0.001 in the left side) were the lowest in
      the AD patients. The left entorhinal cortex of AD patients was smaller also compared to that of SIVD.
      Conclusions: The brain atrophy and the ventricular dilatation can be observed in SIVD as well as
      in AD. However, these findings of SIVD are not from the cortical atrophy such as the hippocampus
      and entorhinal cortex, which is responsible for AD, and might be from the lesions of the white
      matters.

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      다국어 초록 (Multilingual Abstract)

      Background: The findings like the brain atrophy and ventricular dilatation can be also shown on magnetic resonance imaging (MRI) of the patients with subcortical ischemic vascular dementia (SIVD) as well as Alzheimer’s disease (AD), and some patie...

      Background: The findings like the brain atrophy and ventricular dilatation can be also shown on
      magnetic resonance imaging (MRI) of the patients with subcortical ischemic vascular dementia
      (SIVD) as well as Alzheimer’s disease (AD), and some patients with SIVD have the pathology of
      AD. There have been also objected to that SIVD is not the true vascular dementia (VaD), but the
      mixed type with AD. We compared the regional volumes of the gray and white matters between
      AD and SIVD with the hypothesis that the brain atrophy of the patients with SIVD shown on MRI
      is a relative result from the atrophy of the white matter, not from the atrophy of the gray matter.
      Methods: Twelve AD patients and 13 SIVD patients were included in this study. Eleven controls
      without the cognitive impairment were also included. The volumes of the bilateral frontal, temporal,
      parietal areas, and the bilateral hippocampus and entorhinal cortex were obtained. After the correction
      with the ratio to the intracranial volume, the regional volumes were compared among AD,
      SIVD and the controls by analysis of variances with multiple comparisons. Results: Whole brain
      volume of the patients with AD was the smallest (p=0.042). The ventricular volumes of the patients
      with AD and SIVD were smaller than that of the controls (p=0.001). For the volumes of frontal, temporal
      and parietal regions were not different. The volumes of the bilateral hippocampus (p=0.009)
      and entorhinal cortex (p=0.002 in the right side and p=0.001 in the left side) were the lowest in
      the AD patients. The left entorhinal cortex of AD patients was smaller also compared to that of SIVD.
      Conclusions: The brain atrophy and the ventricular dilatation can be observed in SIVD as well as
      in AD. However, these findings of SIVD are not from the cortical atrophy such as the hippocampus
      and entorhinal cortex, which is responsible for AD, and might be from the lesions of the white
      matters.

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      참고문헌 (Reference)

      1 태우석, "청소년기 근간대성간질 환자의 전두엽과 해마 부피의 변화" 대한신경과학회 21 (21): 54-61, 2003

      2 Roman GC, "Vascular dementia: diagnostic criteria for research studies. Report of the NINDS-AIREN International Workshop" 43 : 250-260, 1993

      3 Xu Y, "Usefulness of MRI measures of entorhinal cortex versus hippocampus in AD" 54 : 1760-1767, 2000

      4 Wade JP, "The clinical diagnosis of Alzheimer’s disease" 44 : 24-29, 1987

      5 Roman GC, "Subcortical ischemic vascular dementia" 1 : 426-436, 2002

      6 Braak H, "Staging of Alzheimer’s disease-related neurofibrillary changes" 16 : 271-278, 1995

      7 Erkinjuntii T, "Reserch criteria for subcortical vascular dementia in clinical trials" 59 : 23-30, 2000

      8 Seab JP, "Quantitative NMR measurements of hippocampal atrophy in Alzheimer’s disease" 8 : 200-208, 1988

      9 Kesslak JP, "Quantification of magnetic resonance scans for hippocampal and parahippocampal atrophy in Alzheimer’s disease" 41 : 51-54, 1991

      10 Huther G, "Microanatomic and vascular aspects of the temporomesial region" 43 : 1118-1136, 1998

      1 태우석, "청소년기 근간대성간질 환자의 전두엽과 해마 부피의 변화" 대한신경과학회 21 (21): 54-61, 2003

      2 Roman GC, "Vascular dementia: diagnostic criteria for research studies. Report of the NINDS-AIREN International Workshop" 43 : 250-260, 1993

      3 Xu Y, "Usefulness of MRI measures of entorhinal cortex versus hippocampus in AD" 54 : 1760-1767, 2000

      4 Wade JP, "The clinical diagnosis of Alzheimer’s disease" 44 : 24-29, 1987

      5 Roman GC, "Subcortical ischemic vascular dementia" 1 : 426-436, 2002

      6 Braak H, "Staging of Alzheimer’s disease-related neurofibrillary changes" 16 : 271-278, 1995

      7 Erkinjuntii T, "Reserch criteria for subcortical vascular dementia in clinical trials" 59 : 23-30, 2000

      8 Seab JP, "Quantitative NMR measurements of hippocampal atrophy in Alzheimer’s disease" 8 : 200-208, 1988

      9 Kesslak JP, "Quantification of magnetic resonance scans for hippocampal and parahippocampal atrophy in Alzheimer’s disease" 41 : 51-54, 1991

      10 Huther G, "Microanatomic and vascular aspects of the temporomesial region" 43 : 1118-1136, 1998

      11 Bobeck-Billewicz B, "Magnetic resonance volumetric study of the temporal lobe structures in ischemic vascular dementia" 39 : 15-18, 2001

      12 Barber R, "MRI volumetric study of dementia with Lewy bodies: a comparison with AD and vascular dementia" 54 : 1304-1309, 2000

      13 Bobinski M, "MRI of entorhinal cortex in mild Alzheimer’s disease" 353 : 38-40, 1999

      14 Du AT, "MRI of entorhinal cortex and hippocampus in mild cognitive impairment and Alzheimer’s disease" 71 : 441-447, 2001

      15 Jack CR, "MR-based hippocampal volumetry in the diagnosis of Alzheimer’s disease" 42 : 183-188, 1992

      16 Erkinjuntti T, "Limitations of clinical criteria for the diagnosis of vascular dementia in clinical trials. Is a focus on subcortical vascular dementia a solution?" 903 : 262-272, 2000

      17 Pennanen C, "Hippocampus and entorhinal cortex in mild cognitive impairment and early AD" 25 : 303-310, 2004

      18 Laakso MP, "Hippocampal volumes in Alzheimer’s disease, Parkinson’s disease with and without dementia, and in vascular dementia: an MRI study" 46 : 678-681, 1996

      19 Frisoni GB, "Hippocampal and entorhinal cortex atrophy in frontotemporal dementia and Alzheimer’s disease" 52 : 91-100, 1999

      20 Fein G, "Hippocampal and cortical atrophy predict dementia in subcortical ischemic vascular disease" 55 : 1626-1635, 2000

      21 Du AT, "Effects of subcortical ischemic vascular dementia and AD on entorhinal cortex and hippocampus" 58 : 1635-1641, 2002

      22 Libon DJ, "Declarative and procedural learning, quantitative measures of the hippocampus, and subcortical white alterations in Alzheimer’s disease and ischaemic vascular dementia" 20 : 30-41, 1998

      23 Juottonen K, "Comparative MR analysis of the entorhinal cortex and hippocampus in diagnosing Alzheimer disease" 20 : 139-144, 1999

      24 McKhann G, "Clinical diagnosis of Alzheimer’s disease: report of the NINCDSADRDA Work Group under the auspices of Department of Health and Human Services Task Force on Alzheimer’s Disease" 34 : 939-944, 1984

      25 Lehericy S, "Amygdalohippocampal MR volume measurements in the early stages of Alzheimer disease" 15 : 929-937, 1994

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      학술지 이력

      학술지 이력
      연월일 이력구분 이력상세 등재구분
      2024 평가예정 재인증평가 신청대상 (재인증)
      2021-01-01 평가 등재학술지 선정 (계속평가) KCI등재
      2020-12-01 평가 등재후보로 하락 (재인증) KCI등재후보
      2017-01-01 평가 등재학술지 유지 (계속평가) KCI등재
      2013-01-01 평가 등재 1차 FAIL (등재유지) KCI등재
      2010-01-01 평가 등재학술지 선정 (등재후보2차) KCI등재
      2009-01-01 평가 등재후보 1차 PASS (등재후보1차) KCI등재후보
      2007-01-01 평가 등재후보학술지 선정 (신규평가) KCI등재후보
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      학술지 인용정보

      학술지 인용정보
      기준연도 WOS-KCI 통합IF(2년) KCIF(2년) KCIF(3년)
      2016 0.24 0.24 0.29
      KCIF(4년) KCIF(5년) 중심성지수(3년) 즉시성지수
      0.3 0.24 0.707 0.03
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