Role of the Aβ1-42/Aβ1-40 ratio in the concept 'Alzheimer's disease contributes to mild cognitive impairment'

被引:1
作者
Monge-Garcia, Victoria [1 ]
Llorca-Tolon, Lourdes [2 ]
Gasparini-Berenguer, Ruth [3 ,4 ]
Monge-Argiles, Jose A. [3 ,4 ]
机构
[1] Hosp Gen Univ Alicante, Serv Med Fis & Rehabilitac, Alicante, Spain
[2] Hosp Gen Univ Alicante, Serv Anal Clinicos, Alicante, Spain
[3] Hosp Gen Univ Alicante, Serv Neurol, 8a Planta C, E-03010 Alicante, Spain
[4] Hosp Gen Univ Alicante, Inst Invest Sanitaria & Biomed Alicante ISABIAL, Alicante, Spain
关键词
A beta peptide; Alzheimer's disease; CSF; Mild cognitive impairment; NIA-AA criteria 2018; Ratio A beta; A-BETA-42/40; RATIO; DEMENTIA; CSF; VALIDATION; DIAGNOSIS; CRITERIA; ROUTINE; TAU;
D O I
10.33588/rn.7211.2020594
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Introduction. Evidence of cerebral amyloidosis, by altered levels of the peptide A beta(1-42) or the A beta(1-42)/A beta(1-40) ratio, is a necessary condition to accept the presence of Alzheimer's disease (AD), according to the 2018 criteria of the National Institute on Aging and Alzheimer's Association (NIA-AA 2018). Aim. To calculate the diagnostic gain obtained from calculating the A beta(1-42)/A beta(1-40) ratio with respect to the exclusive use of the peptide A beta(42) to identify patients belonging to the 'Alzheimer's disease contributes to mild cognitive impairment (MCI)' group, according to NIA-AA 2018 criteria. Patients and methods. Between April 2018 and April 2020, we included 62 patients with MCI, according to Petersen's 2006 criteria, who underwent lumbar puncture as part of the diagnostic process. Cerebrospinal fluid was analysed using the immunochemiluminescence methodology, which makes it possible to quantify core AD biomarkers in cerebrospinal fluid and the peptide A beta(1-40). Results. Forty-two patients (67.7%) presented criteria supporting 'AD contributes to MCI'. The use of the A beta(1-42)/A beta(1-40) ratio, compared to the exclusive use of A beta(1-42) levels, represents a diagnostic gain of 19% (eight patients) to establish the presence of amyloidosis in the cerebrospinal fluid of these patients. Conclusion. The calculation of the A beta(1-42)/A beta(1-40) ratio is a clear diagnostic gain for identifying patients belonging to the 'AD contributes to MCI' group, and we therefore recommend its use, as reported in the most recent literature. To our knowledge, this is the first publication of its kind in Spanish.
引用
收藏
页码:371 / 376
页数:6
相关论文
共 19 条
[1]   Revised criteria for mild cognitive impairment: Validation within a longitudinal population study [J].
Artero, Sylvaine ;
Petersen, Ronald ;
Touchon, Jacques ;
Ritchie, Karen .
DEMENTIA AND GERIATRIC COGNITIVE DISORDERS, 2006, 22 (5-6) :465-470
[2]   Addition of the Aβ42/40 ratio to the cerebrospinal fluid biomarker profile increases the predictive value for underlying Alzheimer's disease dementia in mild cognitive impairment [J].
Baldeiras, Ines ;
Santana, Isabel ;
Leitao, Maria Joao ;
Gens, Helena ;
Pascoal, Rui ;
Tabuas-Pereira, Miguel ;
Beato-Coelho, Jose ;
Duro, Diana ;
Almeida, Maria Rosario ;
Oliveira, Catarina Resende .
ALZHEIMERS RESEARCH & THERAPY, 2018, 10
[3]   The added value of Aβ42/Aβ40 in the CSF signature for routine diagnostics of Alzheimer's disease [J].
Biscetti, Leonardo ;
Salvadori, Nicola ;
Farotti, Lucia ;
Cataldi, Samuela ;
Eusebi, Paolo ;
Paciotti, Silvia ;
Parnetti, Lucilla .
CLINICA CHIMICA ACTA, 2019, 494 :71-73
[4]  
Dorey A, 2015, FRONT NEUROL, V6, DOI [10.3389/fneur.2015.00247, 10.3389/tneur.2015.00247]
[5]   Cerebrospinal fluid amyloid-β 42/40 ratio in clinical setting of memory centers: a multicentric study [J].
Dumurgier, Julien ;
Schraen, Susanna ;
Gabelle, Audrey ;
Vercruysse, Olivier ;
Bombois, Stephanie ;
Laplanche, Jean-Louis ;
Peoc'h, Katell ;
Sablonniere, Bernard ;
Kastanenka, Ksenia V. ;
Delaby, Constance ;
Pasquier, Florence ;
Touchon, Jacques ;
Hugon, Jacques ;
Paquet, Claire ;
Lehmann, Sylvain .
ALZHEIMERS RESEARCH & THERAPY, 2015, 7
[6]   Diagnostic Validity Comparison Between Criteria Based on CSF Alzheimer's Disease Biomarkers [J].
Empar Blanco-Canto, Maria ;
Monge-Argiles, J. A. ;
Perez-Cejuela, C. ;
Badia, C. ;
Gabaldon, L. ;
Munoz-Ruiz, C. ;
Sanchez-Paya, J. ;
Gasparini-Berenguer, R. ;
Leiva-Santana, C. .
AMERICAN JOURNAL OF ALZHEIMERS DISEASE AND OTHER DEMENTIAS, 2017, 32 (02) :101-107
[7]   MR SIGNAL ABNORMALITIES AT 1.5-T IN ALZHEIMER DEMENTIA AND NORMAL AGING [J].
FAZEKAS, F ;
CHAWLUK, JB ;
ALAVI, A ;
HURTIG, HI ;
ZIMMERMAN, RA .
AMERICAN JOURNAL OF ROENTGENOLOGY, 1987, 149 (02) :351-356
[8]   Advantages and disadvantages of the use of the CSF Amyloid (A) 42/40 ratio in the diagnosis of Alzheimer's Disease [J].
Hansson, Oskar ;
Lehmann, Sylvain ;
Otto, Markus ;
Zetterberg, Henrik ;
Lewczuk, Piotr .
ALZHEIMERS RESEARCH & THERAPY, 2019, 11 (1) :1-15
[9]   NIA-AA Research Framework: Toward a biological definition of Alzheimer's disease [J].
Jack, Clifford R., Jr. ;
Bennett, David A. ;
Blennow, Kaj ;
Carrillo, Maria C. ;
Dunn, Billy ;
Haeberlein, Samantha Budd ;
Holtzman, David M. ;
Jagust, William ;
Jessen, Frank ;
Karlawish, Jason ;
Liu, Enchi ;
Luis Molinuevo, Jose ;
Montine, Thomas ;
Phelps, Creighton ;
Rankin, Katherine P. ;
Rowe, Christopher C. ;
Scheltens, Philip ;
Siemers, Eric ;
Snyder, Heather M. ;
Sperling, Reisa ;
Elliott, Cerise ;
Masliah, Eliezer ;
Ryan, Laurie ;
Silverberg, Nina .
ALZHEIMERS & DEMENTIA, 2018, 14 (04) :535-562
[10]   Medial temporal lobe atrophy on MRI predicts dementia in patients with mild cognitive impairment [J].
Korf, ESC ;
Wahlund, LO ;
Visser, PJ ;
Scheltens, P .
NEUROLOGY, 2004, 63 (01) :94-100