Improved Cerebrospinal Fluid-Based Discrimination between Alzheimer's Disease Patients and Controls after Correction for Ventricular Volumes

被引:10
|
作者
van Doorn, Linda J. C. van Waalwijk [1 ,2 ,13 ,14 ]
Gispert, Juan D. [3 ,4 ,5 ,13 ,14 ]
Kuiperij, H. Bea [1 ,2 ]
Claassen, Jurgen A. H. R. [6 ]
Arighi, Andrea [7 ]
Baldeiras, Ines [8 ]
Blennow, Kaj [9 ,10 ,11 ]
Bozzali, Marco [12 ]
Castelo-Branco, Miguel [13 ,14 ]
Cavedo, Enrica [16 ]
Emek-Savas, Derya D.
Eren, Erden [18 ]
Eusebi, Paolo [19 ]
Farotti, Lucia [19 ]
Fenoglio, Chiara [7 ]
Ormaechea, Juan Fortea [20 ]
Freund-Levi, Yvonne [21 ,22 ]
Frisoni, Giovanni B. [15 ,23 ,24 ]
Galimberti, Daniela [7 ,17 ]
Genc, Sermin [18 ]
Greco, Viviana [25 ]
Hampel, Harald [16 ]
Herukka, Sanna-Kaisa [26 ,27 ]
Liu, Yawu [26 ,27 ]
Llado, Albert [28 ]
Lleo, Alberto [20 ]
Nobili, Flavio M. [29 ,30 ]
Oguz, Kader K. [31 ]
Parnetti, Lucilla [19 ]
Pereira, Joao [13 ,14 ]
Picco, Agnese
Pikkarainen, Maria [26 ,27 ]
de Oliveira, Catarina Resende [8 ]
Saka, Esen [31 ]
Salvadori, Nicola [19 ]
Sanchez-Valle, Raquel [28 ]
Santana, Isabel [8 ]
Scarpini, Elio [7 ]
Scheltens, Philip [32 ,33 ]
Soininen, Hilkka [26 ,27 ]
Tarducci, Roberto [19 ]
Teunissen, Charlotte [34 ]
Tsolaki, Magda [35 ]
Urbani, Andrea [25 ,36 ]
Vilaplana, Eduard [20 ]
Visser, Pieter Jelle [32 ,33 ,37 ]
Wallin, Asa K. [38 ]
Yener, Gorsev [39 ]
Molinuevo, Jose L. [3 ,40 ]
Meulenbroek, Olga [6 ]
机构
[1] Radboud Univ Nijmegen, Med Ctr, Radboud Alzheimer Ctr, Donders Inst Brain Cognit & Behav,Dept Neurol, Nijmegen, Netherlands
[2] Radboud Univ Nijmegen, Med Ctr, Radboud Alzheimer Ctr, Donders Inst Brain Cognit & Behav,Dept Lab Med, Nijmegen, Netherlands
[3] Pasqual Maragall Fdn, Barcelona Beta Brain Res Ctr, Barcelona, Spain
[4] Ctr Invest Biomed Red Bioingn Biomat & Nanomed CI, Zaragoza, Spain
[5] Pompeu Fabra Univ, Barcelona, Spain
[6] Radboud Univ Nijmegen, Med Ctr, Radboud Alzheimer Ctr, Donders Inst Brain Cognit & Behav,Dept Geriat, Nijmegen, Netherlands
[7] Univ Milan, Fdn Ca Granda, IRCCS Osped Policlin, Milan, Italy
[8] Ctr Hosp Coimbra, Ctr Neurosci & Cell Biol CNC IBILI, Fac Med, Coimbra, Portugal
[9] Univ Coimbra, Coimbra, Portugal
[10] Univ Gothenburg, Sahlgrenska Acad, Inst Neurosci & Physiol, Dept Psychiat & Neurochem, Molndal, Sweden
[11] Sahlgrens Univ Hosp, Clin Neurochem Lab, Molndal, Sweden
[12] IRCCS Santa Lucia Fdn, Neuroimaging Lab, Rome, Italy
[13] Univ Coimbra, Inst Biomed Imaging & Life Sci CNC IBILI, P-3000 Coimbra, Portugal
[14] Univ Coimbra, ICNAS Inst Nucl Sci Appl Hlth, P-3000 Coimbra, Portugal
[15] IRCCS San Giovanni Dio Fatebenefratelli, Lab Epidemiol Neuroimaging & Telemed, Brescia, Italy
[16] Univ Pierre & Marie Curie UPMC Paris 06, Sorbonne Univ,AXA Res Fund & UPMC Chair, Hop Pitie Salpetriere,CNRS,Dept Neurol, Inst Memoire & Malad Alzheimer,IM2A,Inst Cerveau, Blvd Hop, F-75013 Paris, France
[17] Dokuz Eylul Univ, Fac Arts, Hlth Sci Inst, Dept Psychol,Dept Neurosci, Izmir, Turkey
[18] Dokuz Eylul Univ, Izmir Biomed & Genome Inst, Hlth Sci Inst, Dept Neurosci, Izmir, Turkey
[19] Univ Perugia, Ctr Memory Disturbances, Neurol Sect, Perugia, Italy
[20] Hosp Sant Pau, Dept Neurol, Barcelona, Spain
[21] Karolinska Inst, Dept Neurobiol,Caring Sci & Soc NVS, Div Clin Geriatr, Stockholm, Sweden
[22] Karolinska Univ Hosp Huddinge, Dept Geriatr Med, Stockholm, Sweden
[23] United Hosp, Geneva, Switzerland
[24] Univ Geneva, Geneva, Switzerland
[25] IRCCS Fdn Santa Lucia, Prote & Metabol Unit, Rome, Italy
[26] Univ Eastern Finland, Dept Neurol, Kuopio, Finland
[27] Kuopio Univ Hosp, Kuopio, Finland
[28] Hosp Clin Barcelona, IDIBAPS, Neurol Serv, Alzheimers Dis & Other Cognit Disorders Unit, Barcelona, Spain
[29] Univ Genoa, Dept Neurosci DINOGMI, Neurol Clin, Genoa, Italy
[30] IRCCS AOU San Martino IST, Genoa, Italy
[31] Hacettepe Univ, Fac Med, Dept Neurol, Ankara, Turkey
[32] Vrije Univ Amsterdam, Med Ctr, Alzheimer Ctr, Neurosci Campus Amsterdam, Amsterdam, Netherlands
[33] Vrije Univ Amsterdam, Med Ctr, Dept Neurol, Neurosci Campus Amsterdam, Amsterdam, Netherlands
[34] Vrije Univ Amsterdam, Med Ctr, Dept Clin Chem, Neurosci Campus Amsterdam, Amsterdam, Netherlands
[35] Aristotle Univ Thessaloniki, G Papanicolaou Gen Hosp, Memory & Dementia Ctr, Dept Neurol 3, Thessaloniki, Greece
[36] Univ Cattol, Ist Biochim & Biochim Clin, Rome, Italy
[37] Maastricht Univ, Sch Mental Hlth & Neurosci, Alzheimer Ctr Limburg, Dept Psychiat & Neuropsychol, Maastricht, Netherlands
[38] Lund Univ, Dept Clin Sci Malmo, Clin Memory Res Unit, Malmo, Sweden
[39] Dokuz Eylul Univ, Brain Dynam Multidisciplinary Res Ctr, Med Sch Izmir, Biomed & Genome Inst,Dept Neurol, Izmir, Turkey
[40] Hosp Clin Barcelona, IDIBAPS, Neurol Serv, Alzheimers Dis & Other Cognit Disorders Unit, Barcelona, Spain
基金
芬兰科学院; 瑞士国家科学基金会;
关键词
Alzheimer's disease; amyloid biomarkers; cerebrospinal fluid; lateral ventricles; tau protein; MILD COGNITIVE IMPAIRMENT; AD-CSF-INDEX; NATIONAL INSTITUTE; ASSOCIATION WORKGROUPS; DIAGNOSTIC GUIDELINES; BRAIN ATROPHY; BIOMARKERS; DEMENTIA; RECOMMENDATIONS; TAU;
D O I
10.3233/JAD-160668
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Cerebrospinal fluid (CSF) biomarkers may support the diagnosis of Alzheimer's disease (AD). We studied if the diagnostic power of AD CSF biomarker concentrations, i.e., A beta(42), total tau (t-tau), and phosphorylated tau (p-tau), is affected by differences in lateral ventricular volume (VV), using CSF biomarker data and magnetic resonance imaging (MRI) scans of 730 subjects, from 13 European Memory Clinics. We developed a Matlab-algorithm for standardized automated segmentation analysis of T1 weighted MRI scans in SPM8 for determining VV, and computed its ratio with total intracranial volume (TIV) as proxy for total CSF volume. The diagnostic power of CSF biomarkers (and their combination), either corrected for VV/TIV ratio or not, was determined by ROC analysis. CSF A beta(42) levels inversely correlated to VV/TIV in the whole study population (A beta(42): r = -0.28; p < 0.0001). For CSF t-tau and p-tau, this association only reached statistical significance in the combined MCI and AD group (t-tau: r = -0.15; p-tau: r = -0.13; both p < 0.01). Correction for differences in VV/TIV improved the differentiation of AD versus controls based on CSF A beta(42) alone (AUC: 0.75 versus 0.81) or in combination with t-tau (AUC: 0.81 versus 0.91). In conclusion, differences in VV may be an important confounder in interpreting CSF A beta(42) levels.
引用
收藏
页码:543 / 555
页数:13
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