Preserved cognition in patients with early Alzheimer disease and amnestic mild cognitive impairment during treatment with rosiglitazone - A preliminary study

被引:514
作者
Watson, GS
Cholerton, BA
Reger, MA
Baker, LD
Plymate, SR
Asthana, S
Fishel, MA
Kulstad, JJ
Green, PS
Cook, DG
Kahn, SE
Keeling, ML
Craft, S
机构
[1] VAPSHCS, GRECC, Seattle, WA 98108 USA
[2] VAPSHCS, Res & Dev Serv, Seattle, WA 98108 USA
[3] Univ Washington, Sch Med, Dept Psychiat & Behav Sci, Seattle, WA 98195 USA
[4] Univ Washington, Sch Med, Dept Med, Seattle, WA 98195 USA
[5] Univ Washington, Sch Med, Dept Neurol, Seattle, WA 98195 USA
[6] Univ Washington, Sch Med, Dept Psychol, Seattle, WA 98195 USA
[7] Univ Washington, Sch Med, Dept Pharmacol, Seattle, WA 98195 USA
[8] Univ Wisconsin, Sch Med, Dept Med, Madison, WI USA
[9] Univ Wisconsin, GRECC, William S Middleton Mem Vet Hosp, Madison, WI USA
关键词
D O I
10.1176/appi.ajgp.13.11.950
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
Objective: Insulin resistance ( impaired insulin action) has been associated with Alzheimer disease ( AD) and memory impairment, independent of AD. Peroxisome proliferator-activated receptor-gamma ( PPAR-gamma) agonists improve insulin sensitivity and regulate in-vitro processing of the amyloid precursor protein (APP). Authors evaluated the effects of the PPAR-gamma agonist rosiglitazone on cognition and plasma levels of the APP derivative beta-amyloid (A beta) in humans. Methods: In a placebo-controlled, double-blind, parallel-group pilot study, 30 subjects with mild AD or amnestic mild cognitive impairment were randomized to a 6-month course of rosiglitazone ( 4 mg daily; N = 20) or placebo ( N = 10). Primary endpoints were cognitive performance and plasma Ab levels. Results: Relative to the placebo group, subjects receiving rosiglitazone exhibited better delayed recall ( at Months 4 and 6) and selective attention ( Month 6). At Month 6, plasma A beta levels were unchanged from baseline for subjects receiving rosiglitazone but declined for subjects receiving placebo, consistent with recent reports that plasma A beta 42 decreases with progression of AD. Conclusions: Findings provide preliminary support that rosiglitazone may offer a novel strategy for the treatment of cognitive decline associated with AD. Future confirmation in a larger study is needed to fully
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页码:950 / 958
页数:9
相关论文
共 25 条
[1]   Preclinical prediction of AD using neuropsychological tests [J].
Albert, MS ;
Moss, MB ;
Tanzi, R ;
Jones, K .
JOURNAL OF THE INTERNATIONAL NEUROPSYCHOLOGICAL SOCIETY, 2001, 7 (05) :631-639
[2]   Serum insulin-like growth factor I regulates brain amyloid-levels [J].
Carro, E ;
Trejo, JL ;
Gomez-Isla, T ;
LeRoith, D ;
Torres-Aleman, I .
NATURE MEDICINE, 2002, 8 (12) :1390-1397
[3]  
Cohen J., 1988, STAT POWER ANAL BEHA
[4]   Inflammatory mechanisms in Alzheimer's disease:: Inhibition of β-amyloid-stimulated proinflammatory responses and neurotoxicity by PPARγ agonists [J].
Combs, CK ;
Johnson, DE ;
Karlo, JC ;
Cannady, SB ;
Landreth, GE .
JOURNAL OF NEUROSCIENCE, 2000, 20 (02) :558-567
[5]  
CRAFT S, 1993, BEHAV NEUROSCI, V107, P926
[6]   Insulin dose-response effects on memory and plasma amyloid precursor protein in Alzheimer's disease: interactions with apolipoprotein E genotype [J].
Craft, S ;
Asthana, S ;
Cook, DG ;
Baker, LD ;
Cherrier, M ;
Purganan, K ;
Wait, C ;
Petrova, A ;
Latendresse, S ;
Watson, GS ;
Newcomer, JW ;
Schellenberg, GD ;
Krohn, AJ .
PSYCHONEUROENDOCRINOLOGY, 2003, 28 (06) :809-822
[7]   Insulin and neurodegenerative disease: shared and specific mechanisms [J].
Craft, S ;
Watson, GS .
LANCET NEUROLOGY, 2004, 3 (03) :169-178
[8]   Stimulation of β-amyloid precursor protein trafficking by insulin reduces intraneuronal β-amyloid and requires mitogen-activated protein kinase signaling [J].
Gasparini, L ;
Gouras, GK ;
Wang, R ;
Gross, RS ;
Beal, MF ;
Greengard, P ;
Xu, HX .
JOURNAL OF NEUROSCIENCE, 2001, 21 (08) :2561-2570
[9]   Potential roles of insulin and IGF-1 in Alzheimer's disease [J].
Gasparini, L ;
Xu, HX .
TRENDS IN NEUROSCIENCES, 2003, 26 (08) :404-406
[10]   Markers of inflammation and cellular adhesion molecules in relation to insulin resistance in nondiabetic elderly: The Rotterdam study [J].
Hak, AE ;
Pols, HAP ;
Stehouwer, CDA ;
Meijer, J ;
Kiliaan, AJ ;
Hofman, A ;
Breteler, MMB ;
Witteman, JCM .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2001, 86 (09) :4398-4405