Excess of nonceruloplasmin serum copper in AD correlates with MMSE, CSF β-amyloid, and h-tau

被引:164
作者
Squitti, R. [1 ]
Barbati, G.
Rossi, L.
Ventriglia, M.
Dal Forno, G.
Cesaretti, S.
Moffa, F.
Caridi, I.
Cassetta, E.
Pasqualetti, P.
Calabrese, L.
Lupoi, D.
Rossini, P. M.
机构
[1] AFaR Hosp Fatebenefratelli, AFaR Dept Neurosci, I-00186 Rome, Italy
[2] AFaR Hosp Fatebenefratelli, AFaR Dept Radiol, I-00186 Rome, Italy
[3] Univ Roma Tor Vergata, Dept Biol, I-00173 Rome, Italy
[4] Med Coll Wisconsin, Dept Neurol, Milwaukee, WI 53226 USA
[5] Univ Roma La Sapienza, Dept Biochem Sci, I-00185 Rome, Italy
[6] IRCCS, Ctr S Giovanni Dio FBF, Brescia, Italy
[7] Univ Rome, Dept Neurol, Rome, Italy
关键词
D O I
10.1212/01.wnl.0000223343.82809.cf
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective: To assess whether serum copper in Alzheimer disease (AD) correlates with cognitive scores, beta-amyloid, and other CSF markers of neurodegeneration. Methods: The authors studied copper, ceruloplasmin, total peroxide, and antioxidants levels (TRAP) in serum; beta- amyloid in plasma; and copper, beta- amyloid, h-tau, and P-tau in the CSF of 28 patients with AD and 25 healthy controls, in relation to clinical status. Results: Serum copper (p < 0.0001), peroxides (p = 0.002), a copper fraction unexplained by ceruloplasmin (p < 0.0001), and CSF h-tau (p = 0.001) were increased in AD, whereas serum TRAP (p = 0.03) and CSF beta- amyloid were decreased (p < 0.0001). Plasma beta- amyloid increased with age in healthy controls (r = 0.6; p = 0.05). CSF markers of AD correlated with serum copper variables. CSF copper was partially dependent on the serum copper fraction unexplained by ceruloplasmin (t = 2.2, p = 0.04). CSF beta- amyloid seemed to be related to serum copper (r = -0.46; p = 0.002). Mini-Mental Status Examination scores correlated positively with beta- amyloid (r = 0.46, p = 0.002) and inversely with copper unexplained by ceruloplasmin (r = -0.45, p = 0.003). Conclusions: The authors' results confirm the existence of changes in copper component distribution, particularly the copper fraction unexplained by ceruloplasmin and support the hypothesis of a beta-amyloid and copper connection in Alzheimer disease.
引用
收藏
页码:76 / 82
页数:7
相关论文
共 65 条
[1]
ABE A, 1989, CLIN CHEM, V35, P552
[2]
The radical cation of N,N-diethyl-para-paraphenylendiamine:: A possible indicator of oxidative stress in biological samples. [J].
Alberti, A ;
Bolognini, L ;
Macciantelli, D ;
Caratelli, M .
RESEARCH ON CHEMICAL INTERMEDIATES, 2000, 26 (03) :253-267
[3]
Evaluation of CSF-tau and CSF-Aβ42 as diagnostic markers for Alzheimer disease in clinical practice [J].
Andreasen, N ;
Minthon, L ;
Davidsson, P ;
Vanmechelen, E ;
Vanderstichele, H ;
Winblad, B ;
Blennow, K .
ARCHIVES OF NEUROLOGY, 2001, 58 (03) :373-379
[4]
Structure of the Alzheimer's disease amyloid precursor protein copper binding domain - A regulator of neuronal copper homeostasis [J].
Barnham, KJ ;
McKinstry, WJ ;
Multhaup, G ;
Galatis, D ;
Morton, CJ ;
Curtain, CC ;
Williamson, NA ;
White, AR ;
Hinds, MG ;
Norton, RS ;
Beyreuther, K ;
Masters, CL ;
Parker, MW ;
Cappai, R .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (19) :17401-17407
[5]
Structure to function relationships in ceruloplasmin: a 'moonlighting' protein [J].
Bielli, P ;
Calabrese, L .
CELLULAR AND MOLECULAR LIFE SCIENCES, 2002, 59 (09) :1413-1427
[6]
Bishop GM, 2004, BRAIN PATHOL, V14, P448
[7]
Comparison of ultrafiltration and solid phase extraction for the separation of free and protein-bound serum copper for the Wilson's disease diagnosis [J].
Bohrer, D ;
do Nascimento, PC ;
Ramirez, AG ;
Mendonça, JKA ;
De Carvalho, LM ;
Pomblum, SCG .
CLINICA CHIMICA ACTA, 2004, 345 (1-2) :113-121
[8]
Elevation of serum copper levels in Alzheimer's disease [J].
Brenner, S .
NEUROLOGY, 2003, 60 (09) :1559-1559
[9]
The metallobiology of Alzheimer's disease [J].
Bush, AI .
TRENDS IN NEUROSCIENCES, 2003, 26 (04) :207-214
[10]
Metal complexing agents as therapies for Alzheimer's disease [J].
Bush, AI .
NEUROBIOLOGY OF AGING, 2002, 23 (06) :1031-1038