Dissertations / Theses on the topic 'Alcohol withdrawal'
Create a spot-on reference in APA, MLA, Chicago, Harvard, and other styles
Consult the top 43 dissertations / theses for your research on the topic 'Alcohol withdrawal.'
Next to every source in the list of references, there is an 'Add to bibliography' button. Press on it, and we will generate automatically the bibliographic reference to the chosen work in the citation style you need: APA, MLA, Harvard, Chicago, Vancouver, etc.
You can also download the full text of the academic publication as pdf and read online its abstract whenever available in the metadata.
Browse dissertations / theses on a wide variety of disciplines and organise your bibliography correctly.
Canales, Francisco. "Alcohol Withdrawal: Does Sex Matter?" Thesis, The University of Arizona, 2018. http://hdl.handle.net/10150/626845.
Full textRicks, Janet, William H. Repolgle, and Nakia J. Cook. "Clinical Inquiries, Management of Alcohol Withdrawal Syndrome." Digital Commons @ East Tennessee State University, 2010. https://dc.etsu.edu/etsu-works/8811.
Full textHumeniuk, Rachel. "Alcohol withdrawal syndrome : characterisation, predictors of severity, and relationship to relapse /." Title page, contents and abstract only, 1999. http://web4.library.adelaide.edu.au/theses/09PH/09phh9225.pdf.
Full textRichey, Laura. "Behavioral symptoms of withdrawal from acute ethanol exposure possible mediation by inflammatory factors /." Diss., Online access via UMI:, 2008.
Find full textZalud, André W. Diaz-Granados Jamie L. "To giveth and taketh away determination of taurine's protective role during ethanol withdrawal through supplementation and depletion paradigms /." Waco, Tex. : Baylor University, 2008. http://hdl.handle.net/2104/5295.
Full textManley, Samantha Jayne. "Long-term behavioural changes associated with withdrawal from chronic ethanol." Thesis, University of Bristol, 1997. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.361106.
Full textGonzález-Méndez, Wanda Wilma. "Alcohol Use Disorder and Withdrawal Syndrome in Correctional Facilities: An Evidence-Based Clinical Practice Guideline to Prevent Alcohol-Related Adverse Events." ScholarWorks, 2017. https://scholarworks.waldenu.edu/dissertations/4444.
Full textRocha, Ricardo Jorge Nogueira Rodrigues da. "Effect of chronic alcohol consumption and withdrawal in the hippocampal formation." Dissertação, Faculdade de Medicina da Universidade do Porto, 2009. http://hdl.handle.net/10216/53768.
Full textRocha, Ricardo Jorge Nogueira Rodrigues da. "Effect of chronic alcohol consumption and withdrawal in the hippocampal formation." Master's thesis, Faculdade de Medicina da Universidade do Porto, 2009. http://hdl.handle.net/10216/53768.
Full textMacey, Darrel John. "Neurobiological correlates of brain stimulation reward and ethanol withdrawal in the rat /." Diss., Connect to a 24 p. preview or request complete full text in PDF format. Access restricted to UC IP addresses, 2001. http://wwwlib.umi.com/cr/ucsd/fullcit?p3001270.
Full textHelfand, Rebecca S. Diaz-Granados Jamie L. "Taurine depletion in adolescent mice and implications for ethanol withdrawal-induced anxiety." Waco, Tex. : Baylor University, 2007. http://hdl.handle.net/2104/5059.
Full textWatson, William Patrick. "Calcium channel antagonists in the ethanol withdrawal syndrome and other convulsive states." Thesis, University of Bristol, 1994. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.238855.
Full textThomas, Ian Geoffrey, and Ian Geoffrey Thomas. "Identification of Time to Treatment for Alcohol Withdrawal in the Emergency Department." Diss., The University of Arizona, 2017. http://hdl.handle.net/10150/626694.
Full textBarnett, Jared Joshua Anucha. "Weighing the Importance of Vital Signs in the Evaluation of Alcohol Withdrawal in Multiple Ethnicities When Employing the Clinical Institute Withdrawal Assessment." Thesis, The University of Arizona, 2012. http://hdl.handle.net/10150/271614.
Full textSaxon, Lars. "Placebo, alcohol and flumazenil provocations : subjective and objective registrations in psychopharmacological experiments /." Stockholm, 2007. http://diss.kib.ki.se/2007/978-91-7357-077-0/.
Full textRuusa, Jaan. "On testosterone during alcohol withdrawal in men : effects on mood and insulin-like growth factor 1 /." Stockholm, 2004. http://diss.kib.ki.se/2004/91-7140-057-5/.
Full textBurkhardt, Gerrit [Verfasser], and Oliver [Akademischer Betreuer] Pogarell. "Using machine learning to predict individual severity estimates of alcohol withdrawal syndrome in patients with alcohol dependence / Gerrit Burkhardt ; Betreuer: Oliver Pogarell." München : Universitätsbibliothek der Ludwig-Maximilians-Universität, 2021. http://d-nb.info/1238518869/34.
Full textCarter, Megan L. "EXAMINING THE INTERACTION OF NEONATAL ALCOHOL AND HYPOXIA IN VITRO." UKnowledge, 2013. http://uknowledge.uky.edu/psychology_etds/16.
Full textButler, Tracy Renee. "EFFECTS OF CORTICOSTERONE AND ETHANOL CO-EXPOSURE ON HIPPOCAMPAL TOXICITY: POTENTIAL ROLE FOR THE NMDA NR2B SUBUNIT." UKnowledge, 2011. http://uknowledge.uky.edu/gradschool_diss/146.
Full textSharrett-Field, Lynda. "CHARACTERIZING CONSUMPTION, DEPENDENCE, AND THE ROLE OF GLUCOCORTICOIDS IN AN ANIMAL MODEL OF VOLUNTARY ETHANOL CONSUMPTION." UKnowledge, 2013. http://uknowledge.uky.edu/psychology_etds/34.
Full textLaine, P. (Pekka). "Dopamine transporter in alcoholism:a SPET study." Doctoral thesis, University of Oulu, 2001. http://urn.fi/urn:isbn:9514265270.
Full textMaillard, Angéline. "Atteintes cognitives et cérébrales dans le trouble de l'usage d'alcool et le syndrome de Korsakoff : valeur pronostique, évolution et prise en charge Prognosis factors of low-risk drinking and relapse in alcohol use disorder : a multimodal analysis Short-term neuropsychological recovery in alcohol use disorder : a retrospective clinical study Is there cognitive and brain changes over time in Korsakoff's syndrome ? Neuropsychological deficits in alcohol use disorder : impact on treatmen The effect of alcohol withdrawal syndrome severity on sleep, brain and cognition." Thesis, Normandie, 2020. http://www.theses.fr/2020NORMC017.
Full textAlcohol use disorder (AUD) is characterized by brain damage and cognitive deficits. These alterations hinder AUD patients to benefit from psychosocial treatment and increase the risk of relapse. It is now clear that cognitive deficits and brain abnormalities can be reversible with drinking cessation in AUD. However, patients with Korsakoff’s syndrome (KS) are described as exhibiting a severe anterograde amnesia supposed to persist over time, even though longitudinal studies in KS patients are very rare. The objective of this thesis is to examine the prognostic value, changes over time, and rehabilitation of the cognitive impairments and brain alterations in AUD and KS. Our results suggest that alexithymia, as well as alteration of limbic and frontocerebellar systems observed early in abstinence, contribute to a poor prognosis regarding alcohol status within the year following detoxification. We highlight that, after detoxification, a short stay as inpatient in a convalescent home favors cognitive improvement, and even a return to a normal level of performance. During this stay, an intensive care including neuropsychological training seems to favor the recovery. Finally, our results indicate that in KS patients, severe memory impairments, sustained by Papez circuit alterations, persist over time. Executive deficits and damage of the fronto-cerebellar circuit may recover but to a limited extent. These results emphasize the need to assess cognitive and brain alteration that have a prognostic value regarding treatment outcome. Results also encourage adapting treatment to favor recovery in AUD, or to compensate for persisting memory impairments in KS
Laniepce, Alice. "Modifications du sommeil associées à la consommation chronique et excessive d'alcool : liens avec les altérations cérébrales structurales et les troubles cognitifs Neuropsychological and neuroimaging examinations of self‐reported sleep quality in alcohol use disorder with and without Korsakoff's syndrome Sleep architecture and episodic memory performance in alcohol use disorder with and without Korsakoff syndrome The effect of alcohol withdrawal severity on sleep, brain and cognition Dissociating thalamic alterations in alcohol use disorder defines specificity of Korsakoff's syndrome Cerebellar hypermetabolism in alcohol use disorder: compensatory mechanism or maladaptive plasticity ? Alcohol use disorder : permanent and transient effects on the brain and neuropsychological functions Effects of sleep and age on prospective memory consolidation Troubles cognitifs dans l'alcoolodépendance Repérage des troubles cognitifs liés à l’alcool." Thesis, Normandie, 2019. http://www.theses.fr/2019NORMC039.
Full textWell before the development of severe alcohol-related neurological complications such as Korsakoff’s syndrome (KS), patients with Alcohol Use Disorder (AUD) exhibit variable brain damage and cognitive deficits, as well as sleep disturbances. Although it is well established that sleep contributes to brain and cognitive functioning, its involvement in brain damage and cognitive deficits in AUD remains poorly understood. The objective of this thesis was to investigate subjective and objective sleep quality in AUD and KS patients, and its relationships with brain structure and function. Our results show that sleep complaint must be interpreted with regard to the severity of brain alterations and cognitive impairments in AUD and KS patients. Moreover, we showed a high prevalence of sleep apnea in these patients. REM sleep abnormalities are specifically observed in KS patients and related to the severity of memory deficits. Regarding AUD patients, we highlight the contribution of the severity of withdrawal syndrome in slow wave sleep decrease, and its effects on brain and cognitive functioning. Hence, similarities and differences of sleep architecture have been found in the two clinical forms (AUD and KS). These sleep modifications could depend on the severity of alcohol withdrawal and be involved in the pathophysiology of alcohol-related structural brain damage and cognitive impairment. These results encourage evaluating and managing both alcohol withdrawal and sleep modifications to improve patients’ prognosis at discharge from Addiction department
Bachetti, Lívia da Silva. "Ilusão da máscara côncava em pacientes em síndrome de abstinência de álcool leve e moderada." Universidade de São Paulo, 2017. http://www.teses.usp.br/teses/disponiveis/59/59134/tde-30042018-165408/.
Full textThe harmful use of alcoholic beverages is the third largest worldwide risk factor for illness and disability. Alcohol can cause several changes in the Central Nervous System (CNS), among them, the decrease in the processing of visual information. Some studies evaluate changes in perceptual processes during Alcohol Withdrawal Syndrome (AWS) through the hollow face illusion. Its exemplifies the illusory visual depth inversion of a hollow human mask, which is perceived as convex. A possible imbalance was found between the bottomup and top-down components of visual perception caused by alcohol, which could impair the individual\'s ability to perceive the illusion. However, the present research investigates an alternative hypothesis, and suggests that the reduction in the frequency of inversion responses may result from changes in the criteria to issue responses rather than on perceptual changes. The parameters of the Signal Detection Theory (SDT) applied to psychophysics allow this analysis. Twenty healthy subjects, 20 with mild AWS and 20 with moderate AWS participated in the study. They performed two experimental tasks of monocular observation of concave and convex sides, alternately, of a reduced size human face mask. In the task of confidence rating, the concavity or convexity of the mask and the degree of certainty in the answers were judged: certainly or with doubt. In the task of forced choice between two alternatives (2AFC), the masks were presented in alternating pairs and the participant identified the concave side. The analysis of the results revealed that individuals with moderate AWS presented higher scores for the sensitivity index scores R-index, Az, and da, pointing to a significantly greater capacity of identification and discrimination of the concave and convex sides of the mask. This reflects a significant impairment in the ability of these individuals to perceive the hollow face illusion. There was no difference between healthy individuals and with mild AWS. However, all groups with AWS presented a greater degree of certainty in their judgments compared to the control group. Similar results for the group with moderate AWS were found in the task of forced choice to the indices d and hit rate, indicating a greater ability of these individuals to discriminate both sides of the mask. Healthy subjects, on the task of forced choice, showed themselves to be as capable as those with moderate AWS in discriminating both sides of the mask. However, it supposed that these results were from unexpected strategies used by these individuals in their judgments, impairing the internal validity of the results, and represented an important research bias. The analyzes point to a possible imbalance, already reported in previous studies, between the bottom-up and top-down components of visual perception, caused by alcohol, which inhibits the CNS from correcting ambiguous perceptual hypotheses.
Dominguez, Gaëlle. "Impact d'un sevrage à l'alcool sur l'activité du réseau hippocampo-préfrontal au cours d'une épreuve de mémoire de travail : comparaison avec le stress chronique léger imprédictible." Thesis, Tours, 2014. http://www.theses.fr/2014TOUR4029/document.
Full textOur study was aimed to determine the involvement of central corticosterone on the activity of hippocampalprefrontal cortex (HPC-PFC) network and its role in the emergence of working memory (WM) alterations during chronic alcohol consumption (12% for 6 months), or after a short (1 week) or a prolonged (6 weeks) withdrawal periods. The alcohol-withdrawal effects were compared to those resulting from an unpredictable mild chronic stress (UCMS), modeling depression. Our data showed that withdrawal and UCMS, but not alcohol, induced WM disorders and deficits of CREB activation in both the PFC and HPC, and an excessive corticosterone increase specifically in the PFC of withdrawn animals. Pharmacological experiments showed that the inhibition of corticosterone synthesis restored pCREB activity in the PFC of both withdrawn and UCMS mice and improved WM. Furthermore, in withdrawn mice, the increase of pCREB or the blockade of the mineralo-corticoid receptor in the PFC, but not in the HPC, restored WM performance. These results demonstrated that corticosterone dysfunction into the PFC plays a key role in the long-lasting cognitive and neural activity disorders of alcohol-withdrawn mice. We also showed that chronic administration of diazepam reduced such alterations only transitorily. Thus, overall, our study suggests that compounds acting on the GCs activity may constitute alternative strategies to prevent the emergence and maintenance of cognitive disorders induced by alcohol withdrawal
Hård, Julia. "Långvarigt bruk av alkohol ger kramper och epilepsi : Ett arbete om alkohols effekter på hjärnan." Thesis, Linnéuniversitetet, Institutionen för kemi och biomedicin (KOB), 2017. http://urn.kb.se/resolve?urn=urn:nbn:se:lnu:diva-65066.
Full textAlcohol has been used for drinking for many years and is a substance that is well known to most teenagers and adults. Most people also know that alcohol, when misused, can cause damage to both the liver and the kidneys but not as many people know about the damage alcohol can cause the brain. The damage that alcohol causes in the brain can lead to conditions where the patient can experience seizures, whitch can further devlop into epilepsy. Alcohol has different effects on the body. An immidiate response to alcohol is that the inhibitory signaling in the brain increases and the excitatory signaling decreases. When it comes to a prolonged misuse of alcohol the effects on the brain are the opposite and it can also increase the tolerance for alcohol. Inhibitory and excitatory signaling in the brain are essential and disturbance of those signals can be very damaging to the brain. The damages can develop and become permanent and it can also trigger different kinds of seizures. The seizures can in turn become very serious and fatal. Studies on the connection between alcohol and epilepsy has been conducted by Samokhvalov et al. (2010), Devetag et al. (1983), Bråthen et al. (1999), Tartara et al. (1983), Bartolomei et al. (1997), Victor och Brausch (1967) och Hillbom (1980) and have shown different results. The results however have shown a clear correlation between alcohol and epilepsi. In the study performed by Devetag et al. (1983) 58 % of 153 patients experienced seizures not related to alcohol withdrawl, alcohol induction or injury/disease. Of 60 patients who presented seizures in the study conducted by Bartolomei et al. (1997), 30 (50 %) had seizures not related to alcohol withdrawl, alcohol induction or injury/disease. A study performed by Bråthen et al. (1999) showed 16 patients (36 %) of 142 with seizures not related to alcohol withdrawl, alcohol indiction or injury/disease. Furthermore, a study conducted by Tartara et al. (1983) showed 30 patients with seizures, where 3 (10 %) of them were not related to alcohol withdrawl, alcohol induction or injury/disease. Seizures not related to alcohol withdrawl, alcohol abuse or injury/disease are difficult to investigate. Many scientists have tried to get insight in as to how alcohol can influence the ethiopathogenesis of epilepsy. What is alcohol-related seizures, what is the cause behind the seizures and how does one decide if the seizures can be defines as epilepsy. This literature review investigates the link between alcoholism and epilepsy to better understand this connection. The question of issue was ”if prolonged misuse of alcohol can lead to epilepsy” and to unravel the question, 7 studies were used. The studies main focus was alcoholism and seizures. The results from the studies indicated in total that alcohol prabably can cause epilepsy since none of the studies showed the opposite. A prolonged misuse of alcohol can lead to seizures and even epilepsy, but how this comes to be is not clear and needs to be properly investigated. Not to forget, some people who misuse alcohol do not get epilepsy and some never experience even a single seizure.
Feng-Fang, Hung, and 洪芬芳. "Evaluate the effectiveness of applying clinical pathway for the alcohol withdrawal patients." Thesis, 1999. http://ndltd.ncl.edu.tw/handle/92482011477845090601.
Full text國防醫學院
護理研究所
87
The purpose of present study is to explore how clinical pathway affects the following indicators of alcoholic patients in the detoxification state: 1). the length of inpatient stay; 2). inpatient medical costs; 3). dosage of Lorazepam using; 4). readmission rate within a month; 5). patients satisfactory level on medical service; 6). satisfactory level of treatment team , etc. Variance analysis was also applied in the present study. Evaluation was done by Quasi Experimental design; the posttest-only design with nonequivalent group for patients; the one-group pretest-posttest design for treatment team, in order to prove weather there is significance on the indicators of variance after the application of clinical pathway for patients. Forty-four patients of control group, and forty-five patients for experimental group, and eighteen staff of treatment team were pulled by using purposive sampling method. All of the related data was collected during the time of August 1998 and April 1999. Statistic methods such as mean, percentile, independent sampl t-test, paired t-test, chi-square, and multiple-regression, were applied for the present study. Results: The variance of clinical pathway for experimental group was 15.6%, specifically on the factor related to patients or their family members. There were significant differences on duration of stay, medical costs, and the dosage of Lorazepam using. In other words, the experimental group appeared lower medical costs, shorter duration of inpatient stay, and lower dosage of Lorazepam using. There was no significant difference on satisfactory level of patients for medical services and the readmission rate within a month. Further more, staff of the treatment team expressed higher satisfaction on work after applied clinical pathway in the unit. In summary, applying clinical pathway can not only reduce medical costs, improve quality of medical care, but also can increase work related satisfaction among workers. Recommendations: 1. Medical administration: a).The results of applying clinical pathway will be beneficial for arranging proper payment standards and hospital accredited standards b). Systematic information processing procedures should be standardized; c). Medical administrators should be involved and to lead the process of clinical pathway; 2. Education and research: a). It is helpful for research organizations to increase opportunities of educational training regarding clinical pathway; b). the present medical model is suggested to be applied for other types of mental illness; c). the costs related to applying clinical pathway need to be analyzed. 3. Clinical work: a). outcome indicators should be identified in order to evaluate treatment results b). A position for clinical pathway managers should be added; c). The clinical pathway for patients in acute state and the rehabilitation state need to be formulated.
Berman, Ari Ethan. "Brain region gene expression responds discretely to chronic alcohol withdrawal with specific disruption of the hippocampus during intoxication." Thesis, 2005. http://hdl.handle.net/2152/2686.
Full textOzburn, Angela Renee. "Comparison of ethanol-related behaviors and FosB mapping in hybrid mice with distinct drinking patterns." 2009. http://hdl.handle.net/2152/9745.
Full texttext
Chiu, Chia-Ya, and 邱珈雅. "Effects of Methadone on NMDA , GABA Receptors and Taurine Metabolism under Chronic Alcohol Administration and Withdrawal in Astrocytes." Thesis, 2012. http://ndltd.ncl.edu.tw/handle/08571714784808743511.
Full text中國醫藥大學
營養學系碩士班
100
Ethanol is kind of CNS inhibitor, which effects neurotransmitter receeptors such as N-methyl-D-aspartater receptor (NMDARs) and specifically Gamma- aminobutyric acid A receptor (GABAARs) in the brain. Methadone usually reduce damage from heroin withdrawal as substitute medisinms in clinic. The incidence of alcoholism in the MMT patients is 5~50% and found that different drink extent for alcohol administration have different explanation. Taurine participated in brain osmolarity balance , neuroprotective and regulation intracelluler calcium levels ,etc. Moreover, taurine improve the uncomfortable feeling during the alcohol abstinence by astrocytes synthesis. The purpose of the study was to examine whether methadone effects NMDA and GABAA receptors which associated with alcohol administration behavior and synthesis and transpotor of taurine in cultured. Astrocytes were divided into nine group. Except the control and chronic alcohol group, the experimental groups were treated with alcohol medium for 5 days then divided into seven groups by different doses of methadone (0, 0.1, 1, 5, 10μM) , Naltrexone(AN group) and taurine(AT group) for 1 day. After 6 days of treatment , cells were scraped ; cell liquid were collected immediately for analysis of GABA、NMDA receptor subunit ,CSD, TauT, GFAP and taurine levels. The results show that chronic alcohol withdrawal treated 5μM methadone significantly lowered GABAAγ2, GABAAα4, NMDA 2A and NMDA2B subunit levels than AC group. Besides , methadone matained CSD synthesis enzyme levels to enhance taurine levels, and matained taurine to efflux the cell entracelluler by TauT. But taurine levels of the cell entracelluler significantly most lowered than each groups leading to decrease total taurine levels. Based on the results, we conclude that cells treated methadone during chronic alcohol withdrawal effects synthesis and transpotor of taurine a nd modulates alcohol abstinence which resulted variation of type 2 NMDA and GABAA receptor.
Weitzdörfer, Luise [Verfasser]. ""Revised clinical institute withdrawal assessment for alcohol scale" als Prädiktor für die Schwere des Alkoholentzugs / vorgelegt von Luise Weitzdörfer." 2009. http://d-nb.info/1006142894/34.
Full textNeumann, Karoline. "s100β und Homocystein im Serum von stationär behandelten alkoholabhängigen Patienten als Verlaufsvariablen des akuten Alkoholentzugssyndroms." Doctoral thesis, 2014. http://hdl.handle.net/11858/00-1735-0000-0022-5DFF-C.
Full textHuang, Li-Ping, and 黃莉萍. "Study on knowledge, attitude, behavioral intention and self-efficacy of alcohol withdrawal syndrome for taking-care patients’ nurses of one hospital at YILAN county." Thesis, 2015. http://ndltd.ncl.edu.tw/handle/dkn8x3.
Full text國立臺灣師範大學
健康促進與衛生教育學系
103
The purpose of this study is to investigate the knowledge, attitude, behavioral intention and self-efficacy to nurses into take care of the patients suffering alcohol withdrawal syndrome. The research tool used a structured questionnaire which was accepted by National Yang-Ming University Hospital-Institutional Review Board (YMUH- IRB). The participants of this study were the nurses of a regional teaching hospital. Data collected mainly from the questionnaire. A total of 115 valid samples were collected. The recovery ratio is 95.8%. The important results of this research are found as follows: 1.The research objects have good knowledge of alcohol withdrawal syndrome. There are significant difference in knowledge of the level of nursing, seniority and experience of taking care patients who are suffered alcohol withdrawal syndrome. 2.The research objects have good attitude on treatment and management of alcohol withdrawal syndrome. 3.The research objects have good self-efficacy, and there are significant difference in taking care patients who are suffering from alcohol withdrawal syndrome. 4.The research objects have good behavioral intention, and there are significant difference in age, married, the level of nursing, seniority and experience of taking care patients who are suffering from alcohol withdrawal syndrome. 5.Social demographic variables, attitude, self-efficacy of the research objects are to affect the behavioral intention, and there are explained 30% variance.
Lopes, Inês Monteiro. "Polimorfismos genéticos associados com o Delirium Tremens." Master's thesis, 2018. http://hdl.handle.net/10316/82389.
Full textIntrodução: O delirium tremens (DT) é a complicação mais grave da síndroma de abstinência alcoólica (SAA). A prevalência de DT é de 1 a 4% nos indivíduos hospitalizados devido a esta síndroma, estando a sua ocorrência associada a uma mortalidade que oscila entre os 5% e os 15% mesmo sob tratamento apropriado A fisiopatologia do DT é complexa, envolvendo interações entre fatores genéticos e ambientais em indivíduos suscetíveis. A identificação de genes potencialmente associados ao DT tem uma relevância clínica considerável pois permitiria determinar com maior precisão o prognóstico e o risco de DT. Objetivo: Proceder a uma revisão sistemática dos estudos que investigaram a associação entre polimorfismos genéticos e a ocorrência de DT. Métodos: Os estudos relevantes publicados nos últimos 12 anos foram obtidos na base de dados Medline/Pubmed. Foram incluídos estudos de associação caso-controlo e determinados os Odds Ratios e intervalos de confiança.Resultados: O conjunto de trabalhos implicou o estudo de um total de 31 polimorfismos, tendo sido analisados um total de 19 genes em matéria de associação ou não associação com DT. Destes, 6 genes mostraram associação significativa com o desenvolvimento de DT, nomeadamente o gene DBH (dopamina beta-hidroxilase) (OR=2.8, 95%; IC: 0.97–8.1; p=0.056), o gene CHRM2 (receptor muscarínico colinérgico tipo 2) (valor Chi-square= 13.8; p=0.0001), o gene GABRA2 (subunidade alfa-2 do receptor do ácido gama-aminobutírico) (OR = 1.55), e uma interacção entre os genes DRD2 (receptor de dopamina tipo 2) e S1C6A4 (transportador de serotonina) (OR = 0.14, 95%; IC: 0.04–0.52, p=0,003). Nenhum gene candidato mostrou uma associação positiva que fosse reproduzida num estudo diferente dentro desta amostra. Os restantes polimorfismos investigados não mostraram associação significativa com o desenvolvimento de DT.Conclusão: Esta revisão identificou uma variedade de polimorfismos genéticos com associação com o DT, cujos resultados necessitam de ser reproduzidos em amostras de maiores dimensões por forma a serem validados. Neurossistemas como o da transmissão colinérgica e interacções gene-gene entre a transmissão serotoninérgica e dopaminérgica são alvos promissores de investigação futura.
Background: Delirium tremens (DT) is considered to be the most severe complication regarding alcohol withdrawal syndrome (AWS) and it is thought to occur in 1-4% of the alcoholic patients hospitalized with this syndrome. Its ocurrence ranges from 5% to 15% despite appropriate treatment. The genetic aspects with regard to this pathology are rather complex, involving interactions between genetic and environmental factors in susceptible individuals. Identifying genes potentially associated with DT would have significant clinical relevance as it would allow to determine with greater precision the prognosis and risk of DT.Aim: To perform a systematic review of the studies that addressed the association between genetic polymorphisms and DT.Methods: The relevant published studies in the last 12 years have been retrieved from Medline/Pubmed database. We included case-control association studies and determined odds ratio and confidence intervals.Results: The gathered articles had studied a total of 31 genetic polymorphisms in 19 genes regarding the association with DT. 6 genes have shown significant association, namely the DBH gene (dopamine beta-hydroxylase), CHRM2 gene (cholinergic muscarinic receptor type 2), GABRA 2 gene (Gamma-aminobutyric acid receptor subunit alpha-2) and one interaction between the DRD2 gene (dopamine receptor type 2) and SLC6A4 (serotonin trasporter). None of the candidate genes associations have been reproduced in another study inside this pool of articles. The remaining polymorphisms have shown no significant association with DT. Conclusion: This review has identified a variety of genetic polymorphisms with significant association with DT, though there is still a need for replication of the results in larger samples. Neurossystems such as that of the cholinergic transmission and gene-gene interactions between serotoninergic and dopaminergic transmission are promising targets for future research.
Gonçalves, Eugénio António Moita. "Effects of chronic alcohol consumption and withdrawal on the cholinergic neurons of the pedunculopontine and laterodorsal tegmental nuclei of the rat: an unbiased stereological study." Dissertação, 2019. https://hdl.handle.net/10216/119852.
Full textGonçalves, Eugénio António Moita. "Effects of chronic alcohol consumption and withdrawal on the cholinergic neurons of the pedunculopontine and laterodorsal tegmental nuclei of the rat: an unbiased stereological study." Master's thesis, 2019. https://hdl.handle.net/10216/119852.
Full textMalíková, Kristýna. "Sociální práce s mladistvými osobami závislými na psychoaktivních látkách." Master's thesis, 2016. http://www.nusl.cz/ntk/nusl-351462.
Full textPereira, Maria Cecília Paredes. "Toxicodependência e a medicina dentária." Master's thesis, 2016. http://hdl.handle.net/10284/5511.
Full textIntroduction: with the increase in drug abuse, which includes a worldwide problem, also grows the number of patients with their consequences, which are systemic pathologies, including oral health, which is one of the parts of the body suffers from drug addiction. Objectives: this thesis aims to review the literature on "toxicodependence" and "dentistry", correlating these subjects with pathologies and complications in the oral cavity, in particular, bruxism dental wear, xerostomia, halitosis, rampant caries and periodontal disease. Methods: a literature review was conducted on the basis of articles published in journals and theses available in libraries on line, in the last ten years. The keywords were used, as well as the conjugation between them and their proper languages: addiction, detox, withdrawal, cannabis, alcohol, methamphetamine, dental erosion, xerostomia, cavities, bruxism, among others. Conclusion: That there be greater attention and knowledge on the part of the dentist about this condition, as well as of the associated complications, since it is one of the leading health care professionals having contact and the opportunity to treat the symptomatic patients, as well as those who are in the process of recovery and social reintegration.
Lin, Hsiao-Shan, and 林筱珊. "Effects of Soy Protein on Alcoholic Liver Disease in Ethanol-Withdrawal Rats." Thesis, 2010. http://ndltd.ncl.edu.tw/handle/03312234176909761042.
Full text臺北醫學大學
保健營養學研究所
98
Alcoholic liver disease (ALD) is the common consequence of prolong alcohol intake. The metabolism of alcohol generates free radicals which lead to increase oxidative stress, abnormal lipid metabolism, hepatic fat accumulation, and may further cause liver inflammation. The aim of this study is to investigate the effects of soy protein consumption on alcoholic liver disease (ALD). Rats were induced to have ALD with low carbohydrate ethanol liquid diet for 12 weeks and divided into the control group and two experiment groups: the EC group (control liquid diet) and the EP group (control liquid diet + soy protein) for 4 weeks. Diets of the experiment groups contain soy protein as substitution of all of casein. The control group was feed control liquid diet for 16 weeks. After soy protein intervention, we sacrificed partial rats at the 0, 2 and 4 week. Results showed that ethanol group could significantly increase hepatic lipid accumulation and inflammation, and that diet containing soy protein isolate could significantly decrease hepatic lipid, malondialdehyde, pro-inflammatory cytokines, hydroxyproline levels, and myeloperoxidase activity. Additionally, soy protein isolate intake lowered hepatic CYP2E1 protein expression, and increased hepatic PPAR-alpha and CYP4A protein expression. In conclusion, soy protein isolate may improve the alcohol-induced lipid accumulation, oxidative stress, and inflammation by decreasing pro-inflammatory cytokines and CYP2E1 protein expression, and increasing PPAR-alpha and CYP4A protein expression and thereby improve alcoholic liver disease progression.
Maternová, Marcela. "Fenomén alkoholismu a možnosti sociální práce." Master's thesis, 2013. http://www.nusl.cz/ntk/nusl-329302.
Full textNorrish, Maria Elizabeth. "Guidelines for the rehabilitation of the juvenile who had committed a drug-related crime." Thesis, 2011. http://hdl.handle.net/10500/4917.
Full textHealth Studies
D. Litt. et Phil. (Health Studies)
Norrish, Maria Elizabeth. "Guidelines for the rehabilitation of the juveline who had committed a drug-related crime." Thesis, 2011. http://hdl.handle.net/10500/4917.
Full textHealth Studies
D. Litt. et Phil. (Health Studies)
Huang, Ming-Chyi, and 黃名琪. "Differential Patterns of Serum Brain-Derived Neurotrophic Factor Levels and Circadian Rhythm Gene Expression in Alcoholic Patients with and without Delirium Tremens During Acute Withdrawal." Thesis, 2010. http://ndltd.ncl.edu.tw/handle/85732885295130964202.
Full text臺北醫學大學
醫學科學研究所
98
Background: Alcohol withdrawal-enhanced neuroadaptation contributes to the addictive process. Delirium tremens (DTs) is the most serious complication of alcohol withdrawal syndrome (AWS) and postulated to be a clinically distinct phenotype among AWS. Brain-derived neurotrophic factor (BDNF) plays an important role in neuronal plasticity and learning related to addiction. Meanwhile, current evidence indicated a clear interaction between chronic alcohol consumption and disrupted circadian rhythmicity which is regulated by several circadian clock genes including hClock1, hBmal1, hPer1, hPer2, hCry1, hCry2. Studies exploring the altered expressions of these genes in alcohol addiction have been mainly described in animals. Therefore, we assessed the differences in serum BDNF levels as well as the mRNA expression of circadian clock genes, measured at baseline and one week after alcohol withdrawal among alcoholic patients with and without DT. Methods: Sixty-five inpatients, fulfilling the DSM-IV criteria of alcohol dependence and admitted for alcohol detoxification, as well as 39 healthy control subjects were enrolled. The alcoholic patients were further divided by the appearance of DTs into the DT group (n = 25) and non-DT group (n = 40). All the participants received blood withdrawal at 9-10 a.m. while the AD patients had blood collection for twice: on the next morning of admission (baseline) and on the 7th day. Among them, the PBMCs of 22 male alcoholics and 12 comparison control subjects were collected from the whole blood. Serum BDNF levels were measured by sandwich enzyme-linked immunosorbent assay while the mRNA expression profiles of hClock1, hBmal1, hPer1, hPer2, hCry1, hCry2 in PBMCs were determined by quantitative real-time PCR. Results: Serum BDNF levels differed significantly among the three groups: (1) control group 14.8 ± 4.7 ng/mL; (2) non-DT group 12.3 ± 3.3 ng/mL; (3) DT group 6.2 ± 2.6 ng/mL (p < 0.001). After one week after alcohol withdrawal, BDNF levels increased significantly for both alcoholic groups. While non-DT group had comparable BDNF levels (13.4 ± 3.5 ng/mL) with controls, the DT group still exhibited lower levels (8.9 ± 4.4 ng/mL). Regarding to the expression of circadian clock genes, baseline mRNA levels were markedly lower in AD patients than in control subjects. After one week of alcohol detoxification, there were very limited restorations of discrete circadian gene expressions. DT group did not differ in the expression patterns of circadian clock genes from non-DT group. Conclusions: The present study suggests chronic drinking leads to a reduction in BDNF levels and patients with more deficient BDNF expression are vulnerable to the development of DTs. BDNF levels elevated after prompt alcohol detoxification treatment. Therefore BDNF could involve modifying the phenotypes of AWS as well as the pertinent neuroadaptive processes of AD. In addition, we first demonstrated the overall lowering of circadian clock genes among AD patients. But, the expression pattern is comparable between patients with and without DTs. Though preliminary with data at only one single time point, the observation of strikingly reduced mRNA levels supports the association between circadian clock gene dysregulation and chronic alcohol intake.