Plasma amyloid-β levels, cerebral atrophy and risk of dementia: a population-based study

被引:45
作者
Hilal, Saima [1 ,2 ]
Wolters, Frank J. [2 ]
Verbeek, Marcel M. [3 ]
Vanderstichele, Hugo [4 ]
Ikram, M. Kamran [2 ,5 ]
Stoops, Erik [4 ]
Ikram, M. Arfan [1 ,2 ]
Vernooij, Meike W. [1 ,2 ]
机构
[1] Erasmus Univ, Med Ctr, Dept Radiol & Nucl Med, Off 2505,Wytemaweg 80, NL-3015 CN Rotterdam, Netherlands
[2] Erasmus Univ, Med Ctr, Dept Epidemiol, Rotterdam, Netherlands
[3] Radboud Univ Nijmegen, Med Ctr, Dept Neurol & Lab Med, Donders Inst Brain Cognit & Behav,Radboud Alzheim, Nijmegen, Netherlands
[4] ADx NeuroSci, Ghent, Belgium
[5] Erasmus Univ, Dept Neurol, Med Ctr, Rotterdam, Netherlands
关键词
Plasma amyloid-beta levels; Magnetic resonance imaging; Atrophy; Dementia; Population-based; ALZHEIMERS-DISEASE; CEREBROSPINAL-FLUID; HYPOTHETICAL MODEL; DYNAMIC BIOMARKERS; COGNITIVE DECLINE; ELDERLY SUBJECTS; GAMMA-SECRETASE; ROTTERDAM SCAN; ASSOCIATION; PROTEIN;
D O I
10.1186/s13195-018-0395-6
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: Plasma amyloid-beta (A beta) levels are increasingly studied as a potential accessible marker of cognitive impairment and dementia. However, it remains underexplored whether plasma A beta levels including the novel A beta peptide 1-38 (A beta(1-38)) relate to preclinical markers of neurodegeneration and risk of dementia. We investigated the association of plasma A beta(1-38), A beta(1-40), and A beta(1-42) levels with imaging markers of neurodegeneration and risk of dementia in a prospective population-based study. Methods: We analyzed plasma A beta levels in 458 individuals from the Rotterdam Study. Brain volumes, including gray matter, white matter, and hippocampus, were computed on the basis of 1.5-T magnetic resonance imaging (MRI). Dementia and its subtypes were defined on the basis of internationally accepted criteria. Results: A total of 458 individuals (mean age, 67.8 +/- 7.7 yr; 232 [50.7%] women) with baseline MRI scans and incident dementia were included. The mean +/- SD values of A beta(1-38), A beta(1-40), and A beta(1-42) (in pg/ml) were 19.4 +/- 4.3, 186.1 +/- 35.9, and 56.3 +/- 6.2, respectively, at baseline. Lower plasma A beta(1-42) levels were associated with smaller hippocampal volume (mean difference in hippocampal volume per SD decrease in A beta(1-42) levels, -0.13; 95% CI, -0.23 to -0.04; p = 0.007). After a mean follow-up of 14.8 years (SD, 4.9; range, 4.1-23.5 yr), 79 persons developed dementia, 64 of whom were diagnosed with Alzheimer's disease (AD). Lower levels of A beta(1-38) and A beta(1-42) were associated with increased risk of dementia, specifically AD (HR for AD per SD decrease in A beta(1-38) levels, 1.39; 95% CI, 1.00-2.16; HR for AD per SD decrease in A beta(1-42) levels, 1.35; 95% CI, 1.05-1.75) after adjustment for age, sex, education, cardiovascular risk factors, apolipoprotein E epsilon 4 allele carrier status, and other A beta isoforms. Conclusions: Our results show that lower plasma A beta levels were associated with risk of dementia and incident AD. Moreover, lower plasma A beta(1-42) levels were related to smaller hippocampal volume. These results suggest that plasma A beta(1-38) and A beta(1-42) maybe useful biomarkers for identification of individuals at risk of dementia.
引用
收藏
页数:8
相关论文
共 38 条
[1]   Amyloid biomarkers in Alzheimer's disease [J].
Blennow, Kai ;
Mattsson, Niklas ;
Scholl, Michael ;
Hansson, Oskar ;
Zetterberg, Henrik .
TRENDS IN PHARMACOLOGICAL SCIENCES, 2015, 36 (05) :297-309
[2]   Cerebrospinal fluid and plasma biomarkers in Alzheimer disease [J].
Blennow, Kaj ;
Hampel, Harald ;
Weiner, Michael ;
Zetterberg, Henrik .
NATURE REVIEWS NEUROLOGY, 2010, 6 (03) :131-144
[3]   Plasma amyloid-β and risk of Alzheimer's disease in the Framingham Heart Study [J].
Chouraki, Vincent ;
Beiser, Alexa ;
Younkin, Linda ;
Preis, Sarah Rosner ;
Weinstein, Galit ;
Hansson, Oskar ;
Skoog, Ingmar ;
Lambert, Jean-Charles ;
Au, Rhoda ;
Launer, Lenore ;
Wolf, Philip A. ;
Younkin, Steven ;
Seshadri, Sudha .
ALZHEIMERS & DEMENTIA, 2015, 11 (03) :249-257
[4]   Plasma β-Amyloid and Cognitive Decline [J].
Cosentino, Stephanie A. ;
Stern, Yaakov ;
Sokolov, Elisaveta ;
Scarmeas, Nikolaos ;
Manly, Jennifer J. ;
Tang, Ming Xin ;
Schupf, Nicole ;
Mayeux, Richard P. .
ARCHIVES OF NEUROLOGY, 2010, 67 (12) :1485-1490
[5]   Independent generation of Aβ42 and Aβ38 peptide species by γ-secretase [J].
Czirr, Eva ;
Cottrell, Barbara A. ;
Leuchtenberger, Stefanie ;
Kukar, Thomas ;
Ladd, Thomas B. ;
Esselmann, Hermann ;
Paul, Sabine ;
Schubenel, Robert ;
Torpey, Justin W. ;
Pietrzik, Claus U. ;
Golde, Todd E. ;
Wiltfang, Jens ;
Baumann, Karlheinz ;
Koo, Edward H. ;
Weggen, Sascha .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2008, 283 (25) :17049-17054
[6]   The potential for prevention of dementia across two decades: the prospective, population-based Rotterdam Study [J].
de Bruijn, Renee F. A. G. ;
Bos, Michiel J. ;
Portegies, Marileen L. P. ;
Hofman, Albert ;
Franco, Oscar H. ;
Koudstaal, Peter J. ;
Ikram, M. Arfan .
BMC MEDICINE, 2015, 13
[7]   Use of hippocamal and amygdalar volumes on magnetic resonance imaging to predict dementia in cognitively intact elderly people [J].
den Heijer, T ;
Geerlings, MI ;
Hoebeek, FE ;
Hofman, A ;
Koudstaal, PJ ;
Breteler, MMB .
ARCHIVES OF GENERAL PSYCHIATRY, 2006, 63 (01) :57-62
[8]   Cognitively Preserved Subjects with Transitional Cerebrospinal Fluid β-Amyloid 1-42 Values Have Thicker Cortex in Alzheimer's Disease Vulnerable Areas [J].
Fortea, Juan ;
Sala-Llonch, Roser ;
Bartres-Faz, David ;
Llado, Albert ;
Sole-Padulles, Cristina ;
Bosch, Beatriz ;
Antonell, Anna ;
Olives, Jaume ;
Sanchez-Valle, Raquel ;
Molinuevo, Jose L. ;
Rami, Lorena .
BIOLOGICAL PSYCHIATRY, 2011, 70 (02) :183-190
[9]  
GhersiEgea JF, 1996, J NEUROCHEM, V67, P880
[10]   Association of low plasma Aβ42/Aβ40 ratios with increased imminent risk for mild cognitive impairment and Alzheimer disease [J].
Graff-Radford, Neill R. ;
Crook, Julia E. ;
Lucas, John ;
Boeve, Bradley F. ;
Knopman, David S. ;
Ivnik, Robert J. ;
Smith, Glenn E. ;
Younkin, Linda H. ;
Petersen, Ronald C. ;
Younkin, Steven G. .
ARCHIVES OF NEUROLOGY, 2007, 64 (03) :354-362