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1.
Adv Clin Exp Med ; 31(12): 1309-1318, 2022 Dec.
Article in English | MEDLINE | ID: mdl-36047897

ABSTRACT

BACKGROUND: The assessment of motor function is vital in post-stroke rehabilitation protocols, and it is imperative to obtain an objective and quantitative measurement of motor function. There are some innovative machine learning algorithms that can be applied in order to automate the assessment of upper extremity motor function. OBJECTIVES: To perform a systematic review and meta-analysis of the efficacy of machine learning algorithms for assessing upper limb motor function in post-stroke patients and compare these algorithms to clinical assessment. MATERIAL AND METHODS: The protocol was registered in the International Prospective Register of Systematic Reviews (PROSPERO) database. The review was carried out according to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines and the Cochrane Handbook for Systematic Reviews of Interventions. The search was performed using 6 electronic databases. The meta-analysis was performed with the data from the correlation coefficients using a random model. RESULTS: The initial search yielded 1626 records, but only 8 studies fully met the eligibility criteria. The studies reported strong and very strong correlations between the algorithms tested and clinical assessment. The meta-analysis revealed a lack of homogeneity (I2 = 85.29%, Q = 48.15), which is attributable to the heterogeneity of the included studies. CONCLUSION: Automated systems using machine learning algorithms could support therapists in assessing upper extremity motor function in post-stroke patients. However, to draw more robust conclusions, methodological designs that minimize the risk of bias and increase the quality of the methodology of future studies are required.


Subject(s)
Motor Disorders , Stroke Rehabilitation , Stroke , Humans , Upper Extremity , Stroke Rehabilitation/methods , Paresis
2.
Brain Inj ; 35(7): 842-849, 2021 06 07.
Article in English | MEDLINE | ID: mdl-33678100

ABSTRACT

Background: Patients in intensive care units with traumatic brain injuries (TBI) frequently present acid-base abnormalities and coagulability disorders, which complicate their condition.Objective: To identify protonation through in silico simulations of molecules involved in the process of coagulation in standard laboratory tests.Materials and methods: Ten patients with TBI were selected from the intensive care unit in addition to ten "healthy control subjects", and another nine patients as "disease control subjects"; the latter being a comparative group, corresponding to subjects with diabetes mellitus 2 (DM2). Fibrinogen, FVII, FVIII, FIX, FX, and D-dimer in the presence of acidification were evaluated in 20 healthy subjects in order to compare clinical results with molecular dynamics (MD), and to explain proton interactions and coagulation molecules.Results: The TBI group presented a slight, non-significant increase in D-dimer; but this was not present in "disease control subjects". Levels of fibrinogen, FVII, FIX, FX, and D-dimer were affected in the presence of acidification. We observed that various specific residues of coagulation factors "trap" ions.Conclusion: Protonation of tissue factor and factor VIIa may favor anticoagulant mechanisms, and protonation does not affect ligand binding sites of GPIIb/IIIa (PAC1) suggesting other causes for the low affinity to PAC1.


Subject(s)
Brain Injuries, Traumatic , Protons , Blood Coagulation , Brain Injuries, Traumatic/complications , Humans , Molecular Dynamics Simulation
3.
Med Hypotheses ; 144: 110296, 2020 Nov.
Article in English | MEDLINE | ID: mdl-33254487

ABSTRACT

The factors that may contribute to a COVID-19 patient remaining in the asymptomatic stage, or to the infection evolving into the more serious stages are examined. In particular, we refer to the TMPRSS2 expression profile, balance of androgen and estrogen, blood group-A and/or B, nonsynonymous mutations in ORF3, and proteins NS7b and NS8 in SARS-CoV-2. Also, we review other factors related to the susceptibility and pathogenicity of SARS-CoV-2.


Subject(s)
Asymptomatic Infections , COVID-19/genetics , Genetic Predisposition to Disease , SARS-CoV-2 , Serine Endopeptidases/genetics , Alleles , Androgens/metabolism , Angiotensin-Converting Enzyme 2/genetics , COVID-19/virology , Coronavirus RNA-Dependent RNA Polymerase , Exome , Female , Gene Expression Profiling , Histocompatibility Antigens Class I/genetics , Humans , Male , Models, Theoretical , Mutation , Open Reading Frames , Polymorphism, Single Nucleotide , Viral Nonstructural Proteins/genetics , Vitamin D/analogs & derivatives , Vitamin D/metabolism
4.
Indian J Med Res ; 151(1): 11-21, 2020 01.
Article in English | MEDLINE | ID: mdl-32134010

ABSTRACT

Obesity is a serious medical condition worldwide, which needs new approaches and recognized international consensus in treating diseases leading to morbidity. The aim of this review was to examine heterogeneous links among the various phenotypes of obesity in adults. Proteins and associated genes in each group were analysed to differentiate between biomarkers. A variety of terms for classification and characterization within this pathology are currently in use; however, there is no clear consensus in terminology. The most significant groups reviewed include metabolically healthy obese, metabolically abnormal obese, metabolically abnormal, normal weight and sarcopenic obese. These phenotypes do not define particular genotypes or epigenetic gene regulation, or proteins related to inflammation. There are many other genes linked to obesity, though the value of screening all of those for diagnosis has low predictive results, as there are no significant biomarkers. It is important to establish a consensus in the terminology used and the characteristics attributed to obesity subtypes. The identification of specific molecular biomarkers is also required for better diagnosis in subtypes of obesity.


Subject(s)
Biomarkers , Obesity/diagnosis , Obesity/genetics , Proteins/genetics , Adult , Genotype , Humans , Obesity/classification , Obesity/epidemiology , Phenotype
5.
Trop Biomed ; 35(3): 678-683, 2018 Sep 01.
Article in English | MEDLINE | ID: mdl-33601755

ABSTRACT

The chronic indeterminate phase of Chagas' disease is asymptomatic despite positive test results for antibodies specific to Trypanosoma cruzi. CD62P-APC (P-selectin) and PAC-1 FITC (GpIIb/IIIa) may improve diagnosis as biomarkers of platelet activity. Nine asymptomatic seropositive subjects, previously untreated, were selected from a blood bank within a year of Chagas' disease detection, in addition to a control group of four. All subjects were evaluated by flow cytometry for CD62P, PAC-1 and CD41, and in a complementary study, by Tissue Doppler Echocardiography for isovolumic relaxation times (IVRT) and E/A ratios. The subjects were classified as positive or negative for CD62P and PAC-1 by a cut off obtained from their mean±2SD. For IVRT and E/A ratios, cut offs were obtained from the American Society of Echocardiography and the European Association of Cardiovascular Imaging recommendations. Fisher's exact test was used for associated findings. Pre-test and post-test probability, sensitivity, specificity, positive and negative predictive values and likelihood ratios were calculated. Abnormalities were expressed as platelet hyperactivity and ventricular dysfunction in CD62P, PAC-1, IVRT and E/A ratios. CD62P appears to have greater sensitivity (0.75) and PAC-1, more accurate specificity (0.75), which may explain thrombotic events in Chagas' disease. We recommend the use of CD62P and PAC-1 as biomarkers of platelet hyperactivity in patients in the chronic indeterminate phase of Chagas' disease.

7.
Curr Vasc Pharmacol ; 15(3): 207-217, 2017.
Article in English | MEDLINE | ID: mdl-28128064

ABSTRACT

The association between type 2 diabetes mellitus (T2DM) and systemic inflammation may increase platelet reactivity and the accelerated development of vascular disease. Platelets are able to modulate the function of immune cells via the direct release of growth factors and pro-inflammatory chemokines through the production of microvesicles. The microvesicles trigger a transcellular delivery system of bioactive molecules to other cells acting as vectors in the exchange of biological information. Here, we consider the influence of platelets and platelet-derived microvesicles on cells of the immune system and the implications in the pathogenesis of T2DM.


Subject(s)
Blood Platelets/immunology , Cell-Derived Microparticles/immunology , Diabetes Mellitus, Type 2/immunology , Adaptive Immunity , Animals , Blood Platelets/metabolism , Cell-Derived Microparticles/metabolism , Diabetes Mellitus, Type 2/blood , Humans , Immunity, Innate , Inflammation Mediators/blood , Inflammation Mediators/immunology , Oxidative Stress , Signal Transduction
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