Clinical predictors of Alzheimer's disease progression

被引:4
作者
Hishikawa, Nozomi [1 ]
Fukui, Yusuke [1 ]
Takemoto, Mami [1 ]
Sato, Kota [1 ]
Shang, Jingwei [1 ]
Yamashita, Toru [1 ]
Ohta, Yasuyuki [1 ]
Abe, Koji [1 ]
机构
[1] Okayama Univ, Grad Sch Med Dent & Pharmaceut Sci, Dept Neurol, Okayama, Japan
关键词
activities of daily living; apathy; cognitive function; fluctuation; response to medication; DOCOSAHEXAENOIC ACID; COGNITIVE DECLINE; DEMENTIA; RISK; PLASMA; ONSET;
D O I
10.1111/ggi.13286
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
AimRates of disease progression differ among patients with Alzheimer's disease (AD), but prognostic predictions remain a challenge. We carried out a clinic-based retrospective study to investigate the clinical factors for AD progression. MethodsThe 748AD patients, who attended our hospital for >1year and were given the Mini-Mental State Examination (MMSE) at least three times, were divided into three groups according to the annual change rate of MMSE score (G): Aggravater group (G<-2), Stabler group (-2G2) and Improver group (2<G). We compared the three groups on cognitive, affective and activities of daily living functions, response to medication, clinical fluctuations, serum levels of metabolic factors, and neuroimaging data. ResultsWe found no significant differences in age, sex, educational attainment or body mass index across the groups. The Aggravater group showed better baseline MMSE (P<0.01) and Abe's behavioral and psychological symptoms of dementia (P<0.01) scores than the Improver group, but its MMSE improvement after drug treatment was the worst among the three groups (P<0.01 vs Stabler/Improver). Fluctuations in MMSE (P<0.01), apathy scale (P<0.05) and activities of daily living (P<0.01) scores were smaller in the Improver group than in the Aggravater or Stabler groups. Serum docosahexaenoic acid levels tended to be lower (trend P<0.05) and voxel-based specific regional analysis system for Alzheimer's disease Z-scores tended to be higher (trend P<0.05) in the Improver group than in the Stabler or Aggravater groups. ConclusionsInitial responses to medication, fluctuations in cognitive, affective and activities of daily living functions, serum docosahexaenoic acid levels, and medial temporal atrophy are clinical factors related to AD prognosis. Geriatr Gerontol Int 2018; 18: 929-936.
引用
收藏
页码:929 / 936
页数:8
相关论文
共 28 条
[1]   A new simple score (ABS) for assessing behavioral and psychological symptoms of dementia [J].
Abe, K. ;
Yamashita, T. ;
Hishikawa, N. ;
Ohta, Y. ;
Deguchi, K. ;
Sato, K. ;
Matsuzono, K. ;
Nakano, Y. ;
Ikeda, Y. ;
Wakutani, Y. ;
Takao, Y. .
JOURNAL OF THE NEUROLOGICAL SCIENCES, 2015, 350 (1-2) :14-17
[2]   The pleiotropic effects of omega-3 docosahexaenoic acid on the hallmarks of Alzheimer's disease [J].
Belkouch, Mounir ;
Hachem, Mayssa ;
Elgot, Abdeljalil ;
Lo Van, Amanda ;
Picq, Madeleine ;
Guichardant, Michel ;
Lagarde, Michel ;
Bernoud-Hubac, Nathalie .
JOURNAL OF NUTRITIONAL BIOCHEMISTRY, 2016, 38 :1-11
[3]   Docosahexaenoic acid (DHA): a modulator of microglia activity and dendritic spine morphology [J].
Chang, Philip K-Y ;
Khatchadourian, Armen ;
McKinney, Rebecca Anne ;
Maysinger, Dusica .
JOURNAL OF NEUROINFLAMMATION, 2015, 12
[4]   Fatty acid analysis of blood plasma of patients with Alzheimer's disease, other types of dementia, and cognitive impairment [J].
Conquer, JA ;
Tierney, MC ;
Zecevic, J ;
Bettger, WJ ;
Fisher, RH .
LIPIDS, 2000, 35 (12) :1305-1312
[5]   APOE ε4 allele predicts faster cognitive decline in mild Alzheimer disease [J].
Cosentino, S. ;
Scarmeas, N. ;
Helzner, E. ;
Glymour, M. M. ;
Brandt, J. ;
Albert, M. ;
Blacker, D. ;
Stern, Y. .
NEUROLOGY, 2008, 70 (19) :1842-1849
[6]   Effect of cognitive fluctuation on neuropsychological performance in aging and dementia [J].
Escandon, Adriana ;
Al-Hammadi, Noor ;
Galvin, James E. .
NEUROLOGY, 2010, 74 (03) :210-217
[7]   Response of patients with Alzheimer disease to rivastigmine treatment is predicted by the rate of disease progression [J].
Farlow, MR ;
Hake, A ;
Messina, J ;
Hartman, R ;
Veach, J ;
Anand, R .
ARCHIVES OF NEUROLOGY, 2001, 58 (03) :417-422
[8]   ω-3 fatty acid treatment in 174 patients with mild to moderate Alzheimer disease:: OmegAD study -: A randomized double-blind trial [J].
Freund-Levi, Yvonne ;
Eriksdotter-Jonhagen, Maria ;
Cederholm, Tommy ;
Basun, Hans ;
Faxen-Irving, Gerd ;
Garlind, Anita ;
Vedin, Inger ;
Vessby, Bengt ;
Wahlund, Lars-Olof ;
Palmblad, Jan .
ARCHIVES OF NEUROLOGY, 2006, 63 (10) :1402-+
[9]  
Galasko DR, 2000, STAT MED, V19, P1421, DOI 10.1002/(SICI)1097-0258(20000615/30)19:11/12<1421::AID-SIM434>3.3.CO
[10]  
2-G