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1.
Neuroscience ; 498: 280-288, 2022 08 21.
Article in English | MEDLINE | ID: mdl-35716966

ABSTRACT

Cytokines and nitric oxide have been associated with impulsive and aggressive personality traits. We conducted the first study that investigated the role of SNPs in cytokines and nitric oxide genes and the influence in the progression of aggressive and impulsive behavior in 107 of cocaine and crack users. In this case-control, IL-10 (-819C/T), TNFA (-308G/A) and ENOS (-786T/C) polymorphisms were determined by Real-Time PCR. In addition, the relationship between these polymorphisms and Impulsivity and Aggression was determined. We found that the physical aggressiveness sub score was negatively correlated with the C allele of -819C/T polymorphism of the IL-10 (b = -0.14; p = 0.04). The T allele of the SNP -786T/C of the ENOS gene positively predicts traits of physical aggressiveness (b = 0.14; p = 0.04). The GA genotype (b = 0.22; p = 0.01) and the A allele (b = 0.15; p = 0.02) of -308 G/A polymorphism of the TNFA were positively correlated with aggressiveness physical. The GA genotype (b = 0.20; p = 0.03) was positively correlated with aggressiveness verbal. IL-10 (-819C/T), TNFA (-308G/A) and ENOS (-786T/C) polymorphisms might be associated with high risk of aggressive and impulsive behavior.


Subject(s)
Cocaine , Interleukin-10 , Aggression , Case-Control Studies , Cytokines , Genetic Predisposition to Disease , Genotype , Humans , Impulsive Behavior , Nitric Oxide , Nitric Oxide Synthase Type III , Personality , Polymorphism, Single Nucleotide
3.
Clin Pract Epidemiol Ment Health ; 18: e174501792201140, 2022.
Article in English | MEDLINE | ID: mdl-37274848

ABSTRACT

Background: Cocaine/crack use affects immune system molecules and development of mental disorders has been identified. Objective: To investigate the relationship of polymorphisms in the TNFA (-308G/A), IL-10 (-819C/T) and ENOS (-786T/C) genes with mental disorders in cocaine and crack users. Methods: A case-control study was carried out, which included 107 cocaine and crack users and 115 controls who never used healthy cocaine and crack. The SNPs in the TNFA (-308G/A), IL-10 (-819C/T) and ENOS (-786T/C) genes were genotyped by real time PCR. Results: As for the individuals included in this study, the average age of 31.4 years (± 8.59). We identified that the G/A genotype to TNFA (-308) (OR = 0.24; p = 0.03) and the A allele (OR = 0.30; p = 0.03) were associated with reduced risk for dysthymic disorder. The T allele of the IL-10 (-819) polymorphism was associated with decreased risk of developing panic disorder (OR = 0.44; p = 0.01), while the C allele was correlated with an increased risk for alcohol dependence (OR = 1.97; p = 0.04), alcohol abuse (OR = 1.81; p = 0.04) and psychotic syndrome (OR = 2.23; p = 0.01). C/C genotype was correlated with increased chances of developing current psychotic syndrome (OR = 4.23; p = 0.01). Conclusion: Our results suggest that genetic polymorphisms promote susceptibility or promote protection for clinical phenotypes of psychiatric comorbidities in cocaine and crack users and be considered as good prognostic markers.

4.
Recent Pat Biotechnol ; 15(3): 169-183, 2021.
Article in English | MEDLINE | ID: mdl-34353276

ABSTRACT

Extremophilic microorganisms from a wide variety of extreme natural environments have been researched, and many biotechnological applications have been carried out, due to their capacity to produce biomolecules resistant to extreme conditions, such as fibrinolytic proteases. The search for new fibrinolytic enzymes is important in the development of new therapies against cardiovascular diseases. This article aimed to evaluate the patents filed about protease with fibrinolytic activity produced by extremophilic microorganisms whose use is aimed at the development of new drugs for the treatment of cardiovascular diseases. The prospecting was carried out using data on deposits and patent concessions made available on the technological bases: European Patent Office (EPO), United States Patent and Trademark Office (USPTO), World Intellectual Property Organization (WIPO), Instituto Nacional de Propriedade Industrial - Brazil (INPI), The LENS and Patent Inspiration. The International Patent Classification and subclasses and groups for each document were also evaluated. Although 382 patents were selected using terms related to extreme environments, such as "thermophile" and "acidophiles", few were related to clinical use and were mainly performed using Bacillus subtilis and Streptomyces megasporus strains. A highlight of nattokinase was produced by Bacillus subtilis GDN and actinokinase by Streptomyces megasporus SD5. The low number of patents on enzymes with this profile (extreme environments) revealed a little-explored field, promising in the development of new microbial thrombolytic drugs, such as fibrinolytic enzymes with less adverse effects.


Subject(s)
Extremophiles , Biotechnology , Intellectual Property , Patents as Topic , Thrombolytic Therapy , United States
5.
Recent Pat Biotechnol ; 15(4): 250-265, 2021.
Article in English | MEDLINE | ID: mdl-34353277

ABSTRACT

BACKGROUND: L-asparaginase (L-ASNase, L-asparagine amidohydrolase, E.C.3.5.1.1) is an enzyme with wide therapeutic applicability. Currently, the commercialized L-ASNase comes from mesophilic organisms, presenting low specificity to the substrate and limitations regarding thermostability and active pH range. Such factors prevent the maximum performance of the enzyme in different applications. Therefore, extremophilic organisms may represent important candidates for obtaining amidohydrolases with particular characteristics desired by the biotechnological market. OBJECTIVES: The present study aims to carry out a technological prospecting of patents related to the L-asparaginases derived from extremophilic organisms, contributing to pave the way for further rational investigation and application of such enzymes. METHODS: This patent literature review used six patents databases: The LENS, WIPO, EPO, USPTO, Patent Inspiration, and INPI. RESULTS: It was analyzed 2860 patents, and 14 were selected according to combinations of descriptors and study criteria. Approximately 57.14% of the patents refer to enzymes obtained from archaea, especially from the speciesPyrococcus yayanosii (35.71% of the totality). CONCLUSION: The present prospective study has singular relevance since there are no recent patent reviews for L-asparaginases, especially produced by extremophilic microorganisms. Although such enzymes have well-defined applications, corroborated by the patents compiled in this review, the most recent studies allude to new uses, such as the treatment of infections. The characterization of the catalytic profiles allows us to infer that there are potential sources still unexplored. Hence, the search for new L-ASNases with different characteristics will continue to grow in the coming years and, possibly, ramifications of the technological routes will be witnessed.


Subject(s)
Asparaginase , Extremophiles , Asparagine , Biotechnology , Patents as Topic , Prospective Studies
6.
Infect Genet Evol ; 93: 104846, 2021 09.
Article in English | MEDLINE | ID: mdl-33933633

ABSTRACT

The Severe acute respiratory syndrome may be caused by coronavirus disease which has resulted in a global pandemic. Polymorphisms in the population play a role in susceptibility to severity. We aimed to perform a systematic review related to the effect of single nucleotide polymorphisms in the development of severe acute respiratory syndrome (SARS). Twenty-eight eligible articles published were identified in PubMed, ScienceDirect, Web of Science, PMC Central and Portal BVS and additional records, with 20 studies performed in China. Information on study characteristics, genetic polymorphisms, and comorbidities was extracted. Study quality was assessed by the STrengthening the REporting of Genetic Association (STREGA) guideline. Few studies investigated the presence of polymorphisms in HLA, ACE1, OAS-1, MxA, PKR, MBL, E-CR1, FcγRIIA, MBL2, L-SIGN (CLEC4M), IFNG, CD14, ICAM3, RANTES, IL-12 RB1, TNFA, CXCL10/IP-10, CD209 (DC-SIGN), AHSG, CYP4F3 and CCL2 with the susceptibility or protection to SARS-Cov. This review provides comprehensive evidence of the association between genetic polymorphisms and susceptibility or protection to severity SARS-CoV. The literature about coronavirus infection, susceptibility to severe acute respiratory syndrome (SARS) and genetic variations is scarce. Further studies are necessary to provide more concrete evidence, mainly related to Covid-19.


Subject(s)
COVID-19/genetics , Polymorphism, Genetic , Chemokines/genetics , Cytokines/genetics , Female , Genetic Association Studies , Genetic Markers , Genetic Predisposition to Disease , HLA Antigens/genetics , Humans , Male , Mannose-Binding Lectin/genetics
7.
Immunol Invest ; 50(1): 58-79, 2021 Jan.
Article in English | MEDLINE | ID: mdl-32204641

ABSTRACT

Background: Chikungunya virus (CHIKV) is a global concern, inducing chikungunya fever and trigging an arthritogenic chronic phase beyond some severe forms. Outcomes of CHIKV infections in humans are dependent on genetic variations. Here, a systematic review was performed to show evidence of genetic variations on infection outcomes of patients. Methods: Searches were performed in Scopus, SciELO, MEDLINE/PubMed, Web of Science, OneFile (GALE), Periódicos CAPES and ScienceDirect Journals databases. The PICOS approach was used to assess the eligibility of records. A meta-analysis was also conducted to show an association between described alleles/genes and CHIKV infection outcome. Results: Reviews of genetic variants were conducted on genes: CD 209, OAS1, OAS2, OAS3, MIF, TLR-3, TLR-7, TLR-8, MYD-88, KIR, HLA-B; HLA-C; DRB1 and DQB1. Studies were performed on Gabon, Singapore, and India, including Indians, Malay, Gabonese and Chinese ethnicities and published between 2009-2017. The meta-analysis was performed with DRB1 *01; *03; *04; *07; *10; *11; *13; *14 and *15 and DQB1 *02; *03; *05 and *06 alleles with Indian population sample. Sampling power was >80% and a significant positive association between DRB1*14 and CHIKV infection was found (OR = 1.67, 95% CI = 1.04-2.67; p = .03). Conclusion: Majority of the studies were conducted in India. Meta-analysis suggests that DRB1*14 is related to the susceptibility of symptomatic CHIKV infection in Indian population. The literature about CHIKV infection and genetic variations is scarce. The precise role of genetic variation in CHIKV is not clear yet. Further studies are necessary to provide more concrete evidences.


Subject(s)
Chikungunya Fever/genetics , Chikungunya Fever/virology , Chikungunya virus/physiology , Host-Pathogen Interactions/genetics , Alleles , Chikungunya Fever/epidemiology , Disease Susceptibility , Genetic Predisposition to Disease , Histocompatibility Antigens Class II/genetics , Humans , Odds Ratio , Patient Outcome Assessment , Polymorphism, Genetic , Prognosis
8.
Immunol Invest ; 50(5): 492-526, 2021 Jul.
Article in English | MEDLINE | ID: mdl-32602796

ABSTRACT

Objectives: This study investigated the relationship between single-nucleotide polymorphisms (SNPs) in cytokine genes and the susceptibility to Squamous Intraepithelial Lesions (SIL), cervical cancer and HPV infection through a systematic review with meta-analysis. To verify the effect of SNPs, we also analyzed the transcription factor binding affinity using bioinformatics tools.Methods: Seven electronic databases (MEDLINE, Scielo, BIREME, PubMed, Scopus, Web of Science and Science Direct) were searched for case-control studies.Results: A total of 35 relevant case-control studies were meta-analyzed, including 7 cytokine genes and 15 SNPs. SNPs in IL-17A (rs2275913, rs3748067); IL-17 F (rs763780); IL-12A (rs568408); IL-12B (rs3212227); TNFA (rs1800629, rs361525); IL-1B (rs16944); IL-6 (rs1800795); IL-10 (rs1800896) genes were associated with increased risk for cervical cancer. No association was observed between meta-analyzed polymorphisms and SIL. Additional bioinformatics analysis suggested a possible transcriptional regulation pathway of the TNFA and IL-10 genes through the MZF1 (TNFA -308 G > A and IL-10 - 1082A>G) and ZNF263 (TNFA -238 G > A) transcription factors binding.Conclusion: Overall, 10 SNPs in cytokine genes were associated with increased risk for cervical cancer. Therefore, in our meta-analysis, these SNPs demonstrated to be potential biomarkers for predicting or identifying cases of high risk for SIL and cervical cancer.


Subject(s)
Alphapapillomavirus/physiology , Cytokines/genetics , Papillomavirus Infections/genetics , Precancerous Conditions/genetics , Squamous Intraepithelial Lesions of the Cervix/genetics , Uterine Cervical Neoplasms/genetics , Computational Biology , Female , Genetic Predisposition to Disease , Humans , Papillomavirus Infections/immunology , Polymorphism, Single Nucleotide , Risk , Squamous Intraepithelial Lesions of the Cervix/immunology , Uterine Cervical Neoplasms/immunology
9.
Acta Trop ; 190: 144-148, 2019 Feb.
Article in English | MEDLINE | ID: mdl-30452889

ABSTRACT

Serotonin and nitric oxide seem to be involved in Dengue virus infection. The aim of this study was to investigate if SNPs in serotonin and nitric oxide are associated with dengue severity. A retrospective case-control study was conducted, with groups of dengue fever (DF; n = 78) and dengue hemorrhagic fever patients (DHF; n = 49). Genotyping was performed using qPCR and PCR. The power of the sample size was calculated by G*power software. The heterozygous SL for 5-HTTLPR SNP was significantly correlated with protection against progression to DHF in the codominant SS/SL/LL (OR = 0.22, 95% CI = 0.06-0.81, p = 0.011) and overdominant models SL vs SS + LL (OR = 0.19, 95% CI = 0.06-0.65, p = 0.003). For the ENOS (rs1799983) SNP, the genotype GT was positively associated with protection for development of the clinical form in DHF compared to dengue fever (OR = 0.39, 95% CI = (0.13-1.14), p = 0.0058) in codominant GG/GT/TT and overdominant model GT vs GG + TT (OR = 0.35, 95% CI = (0.12-1.02), p = 0.04). To our knowledge, this is the first study to identify the association of the serotonin and nitric oxide SNPs with dengue severity.


Subject(s)
Nitric Oxide Synthase Type III/genetics , Serotonin Plasma Membrane Transport Proteins/genetics , Severe Dengue/genetics , Adolescent , Adult , Alleles , Brazil , Case-Control Studies , Disease Progression , Female , Genotype , Humans , Male , Middle Aged , Polymorphism, Single Nucleotide , Protective Factors , Retrospective Studies , Young Adult
10.
Rev Bras Med Trab ; 15(4): 310-316, 2017.
Article in English | MEDLINE | ID: mdl-32377586

ABSTRACT

BACKGROUND: The study of the profile of medical records of tobacco growers contributes to discussions on the establishment of diagnosis and its causal correlation with work. OBJECTIVE: To investigate the profile of clinical information in medical records of tobacco growers. METHODS: The present was a descriptive field and documentary study, with quantitative approach, of 149medical records of farmers who visited basic health units in rural communities in the municipality of Arapiraca, Alagoas, Brazil, from 2008 to 2013. RESULTS: About 66% of the investigated population was female, with average age 58.6 years old (standard deviation ±16.4). The most significant clinical complaint found in the records was headache (16.71%), followed by low back pain (10.20%), dysuria or other urinary problems (8.90%) and stomachache (8.30%). Medical diagnoses included gastritis (15.1%), depression (7.1%), anxiety (7.1%), myalgia (7.1%) and arthritis/arthralgia (5.3%). Correlation between clinical complaints and work performed by tobacco growers was registered on one single medical record. CONCLUSION: The clinical profile of tobacco growers described in the medical records might be associated with their social and working conditions and related to pesticide and nicotine poisoning. However, the scarcity of information on the environmental and occupational risk context limits the establishment of a causal link. As a function of the relevance of the occupational-clinical conditions of this population of workers, improving medical records is necessary, as the temporal relationship between exposure and outcomes might account for the occurrence of the reported symptoms.


INTRODUÇÃO: O estudo do perfil dos registros clínicos em prontuários de fumicultores favorece a discussão do estabelecimento do diagnóstico e do nexo causal com o trabalho. OBJETIVO: Identificar o perfil dos registros clínicos em prontuários de fumicultores. MÉTODO: Trata-se de um estudo descritivo de campo e documental com abordagem quantitativa dos registros em 149 prontuários de fumicultores que frequentaram Unidades Básicas de Saúde da Família de comunidades rurais do município de Arapiraca, Alagoas, no período de 2008 a 2013. RESULTADOS: Foi identificado que 66% dos usuários são do sexo feminino, com média de idade de 58,6 anos (desvio padrão - DP±16,4). As queixas clínicas mais expressivas registradas nos prontuários estavam relacionadas à cefaleia (16,71%), seguida por dor lombar (10,20%), disúria ou outros problemas urinários (8,90%) e epigastralgia (8,30%). Quanto aos diagnósticos médicos, destacaram-se gastrite/epigastralgia (15,1%), depressão (7,1%), ansiedade (7,1%), mialgia (7,1%) e artrite/artralgia (5,3%). A correlação das queixas clínicas como trabalho desenvolvido pelos fumicultores foi registrada em apenas um prontuário. CONCLUSÃO: O perfil clínico dos fumicultores apresentado nos prontuários poderia estar associado às condições sociais e de trabalho e inter-relacionado com a intoxicação por agrotóxicos e nicotina. Porém, a escassez de registros contextualizando o ambiente e os riscos ocupacionais torna limitante o nexo causal. Pela relevância do quadro clínico-ocupacional desses trabalhadores, faz-se necessária a melhoria dos registros, o que poderia justificar os sintomas apresentados levando em consideração as relações temporais entre a exposição e o desfecho.

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