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Abbreviations: AD, alzheimer’s disease; CDR, clinical
dementia rating; MNA, mini nutritional assessment; HDL, high density
lipoprotein; LDL, low density lipoprotein levels; Aβ, accumulation of
beta-amyloid; NINCDS-ADRDA, national institute of neurologic and
communicative disorders and stroke and the alzheimer disease and
related disorders association; MMSE, mini-mental state exam; ALT,
alanine transaminase; AST, aspartate transaminase; CBC, complete
blood count
Introduction
Alzheimer’s disease (AD) is a neurodegenerative disease
which presents synaptic loss and neural death, resulting in cerebral
atrophy, with consequent and gradual loss of memory and cognitive
impairment, individual incapacity and progressive disability.
1,2
AD
has, as post-mortem markers, insoluble aggregates of β-amyloid
peptides and insoluble flaments composed of hyper phosphorylated
tau protein.
3
To obtain blood samples from patients, such as serum,
plasma and circulating cells is simple, therefore these are considered
potential sources of biomarkers for AD diagnosis, research and
clinical practice.
4,5
Plasmatic elements such as enzymes, glucose and
lipids have been widely studied in AD´s patients.
6
Such plasmatic
compounds would allow the implementation of effective preventive
and therapeutic measures during the early stages of the disease, long
before substantial cognitive impairment and brain structure´s decline.
Analyses of nutritional blood components and the monitoring
of other conditions, have contributed to improve AD’s pathological
progression understanding. According to Vetrivel and Thinakaran,
total cholesterols levels and low density lipoprotein levels (LDL) in
serum correlate with the accumulation of Beta-amyloid (Aβ) peptides
in the brain of patients with AD.
7
Micronutrients, such as selenium
and zinc, B vitamins and antioxidant vitamins have being described
as fundamental elements for cerebral neuroprotection and cognitive
function in elderly people.
8
According to Chen e Zhong, metabolism
dysfunctions of cerebral glucose can be fundamental contributors
to the pathogenesis of the disease, through the induction of various
factors such as oxidative stress and mitochondrial dysfunction,
in addition its occurrence precedes cognitive dysfunction and
pathological changes even over the decades.
9
However, the diffculty
of developing a biomarker based in blood for AD is marked by
the fact that Alzheimer’s is a disease that progresses slowly and
heterogeneously, since mixed pathologies are observed frequently.
10
Considering such evidences, this study aimed to investigate
the relation between biochemical and hematological parameters
commonly used in clinical practices, such as lipid profles, hepatic
enzymes, glucose and CBC in patients with Alzheimer’s disease, and
also correlate them with the different stages of the disease and the
nutritional status of the patients.
Materials and methods
This study was conducted with AD patients, registered in the
“Specialized Component of Pharmaceutical Assistance” of the Health
Ministry of Guarapuava, Parana, Brazil, from August to October
2011. Initially, 66 subjects were recruited in the program, with
probable diagnosis of AD, according to the criteria of the National
Institute of Neurologic and Communicative Disorders and Stroke and
the Alzheimer Disease and Related Disorders Association (NINCDS-
Hos Pal Med Int Jnl. 2017;1(4):90‒95 90
© 2017 Fermino et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which
permits unrestricted use, distribution, and build upon your work non-commercially.
Potential biomarkers for alzheimer’s disease
screened in a small Brazilian population
Volume 1 Issue 4 - 2017
Bárbara Luísa Fermino,
1
Jéssica Wouk,
1
Roberta Fabbli,
2
Weber Claúdio Francisco
Nunes da Silva,
1
José Carlos Rebuglio
Vallosa,
3
Juliana Sartori Bonini,
1
Luan
Henrique Patrzyk,
4
Anne Karine Bosetto,
5
Flávia Ivansk
5
1
Pharmacy Department, Midwest State University, Brazil
2
Department of Neuroscience, University of Florence, Italy
3
Department of Clinical and Toxicological Analysis, State
University of Ponta Grossa, Brazil
4
Department of Physiotherapy, Midwest State University, Brazil
5
Department of Biological Sciences, Federal University of Rio
Grande do Sul, Brazil
Correspondence: Juliana Sartori Bonini, Pharmacy
Department, Midwest State University, Simeão Camargo Varella
de Sá Street, Guarapuava, Paraná, Brazil,
Email Juliana.bonini@gmail.com
Received: September 26, 2017 | Published: October 06, 2017
Abstract
Alzheimer’s Disease (AD) leads neurodegenerative diseases ranking and, because
of this, clinical attention focus on the identification of blood, serum and plasma’
biomarkers in AD patients, since diagnostic have not a gold standard yet. In order
to improve diagnose, current study explore relation between biochemical and
hematological’ parameters, which are commonly applied as lipid profile, liver
enzymes, glucose and hemogram. Furthermore, different stages of AD have been
evaluated through Clinical Dementia Rating (CDR) and Mini Nutritional Assessment
(MNA) evaluated nutritional status, since nutritional status interferes directly in
parameters reached. For this purpose, this study included 30 patients, being 18(60%)
women and 12(40%) men, in different stages of AD. Our data report that malnutrition
level is directly related with disease progression, as discussed in literature over the
years. With regard to hematological analysis, significate difference was observed
between parameters and groups, where patients in moderate stage of disease improved
erythrocytes and had greater values of globular volume when compared to final stage,
suggesting that AD is a possible risk factor to anemia. Biochemical data also presented
significate difference, showing that disease progression, High Density Lipoprotein
(HDL) values and total cholesterol are directly proportional. Take into consideration
significate differences from this study and since AD means a heterogeneous disease,
more studies are needed to validate in vivo essays that may be relevant to identify this
disease.
Keywords: alzheimer disease, biomarkers, neurodegeneration, biochemistry,
nutrition
Hospice and Palliative Medicine International Journal
Research Article
Open Access