Avaliação cognitiva em traumatizados crânio-encefálicos ligeiros

O aumento da incidência de traumatismos crânio-encefálicos (TCE) a nível internacional, tem vindo a fomentar o desenvolvimento de estudos neste domínio. O presente estudo pretende determinar a deterioração cognitiva e o estado depressivo em indivíduos com TCE ligeiro e sem TCE; analisar a deterioração cognitiva e o estado depressivo nos indivíduos com TCE ligeiro e sem TCE em relação ao sexo, idade, estado civil, residência e tipo de traumatismo; analisar a relação entre a deterioração cognitiva e o estado depressivo dos indivíduos com TCE e o tipo de traumatismo sofrido. Através de um estudo comparativo, avaliamos uma amostra total de 40 indivíduos, tendo o emparelhamento sido feito entre 2 grupos:  grupo clínico: 20 indivíduos com TCE ligeiro (entre 6 e 18 meses após lesão) com idades compreendidas entre os 18 e os 65 anos;  grupo de controlo: 20 indivíduos sem ter tido TCE ou patologia conducente a handicap psiquiátrico ou neurológico. A deterioração cognitiva foi avaliada através do Mini Mental State Examination (Folstein et al., 1975-versão portuguesa, adaptada por Guerreiro, 1993) que é um teste constituído por seis grupos que avaliam o defeito cognitivo do sujeito. Também foi utilizada a Bateria de Avaliação Neuropsicológica de Luria- Nebraska / versão experimental portuguesa de Maia, Loureiro e Silva, 2002, traduzida e adaptada de Golden, Hammeke e Purisch, 1979, que é uma bateria que visa avaliar o funcionamento neuropsicológico de indivíduos com manifestações neuropsicológicas. O estado depressivo foi avaliado através do Inventário de Avaliação Clínica da Depressão-IACLIDE (Serra, 1994) que mede a intensidade dos quadros clínicos depressivos, bem como uma ficha de registo individual de dados biográficos e clínicos. Os principais resultados são: Os indivíduos do grupo clínico, ou seja, aqueles que sofreram TCE ligeiro evidenciam maior deterioração cognitiva comparativamente com os que o não sofreram. Aqueles indivíduos também evidenciam estados depressivos significativamente mais graves do que os indivíduos que não sofreram aquele traumatismo. O TCE ligeiro induz um aumento dos sintomas depressivos em termos biológicos, cognitivos, inter-pessoais e desempenho de tarefas e tende a agravar os níveis de depressão endógena e a causar perturbação na relação do indivíduo consigo próprio; O TCE ligeiro conduz a um aumento significativo da incapacidade dos indivíduos para a vida geral, para o trabalho, para a vida social e para a vida familiar; Os indivíduos que sofreram TCE ligeiro evidenciam funções motoras, linguagem expressiva e raciocínio aritmético mais perturbadas que os que o não sofreram; O TCE ligeiro induz alterações neuropsicológicas que diminuem significativamente a capacidade dos mesmos. Os dados obtidos indicam, que os indivíduos que sofreram TCE do sexo feminino evidenciaram alteração cognitiva mais acentuada do que os do sexo masculino; os indivíduos mais velhos que sofreram TCE ligeiro, tendem a evidenciar maior deterioração do estado cognitivo e avaliação neuropsicológica mais baixa; verificamos também que no grupo clínico os indivíduos casados revelaram pior estado neuropsicológico na escala da bateria referente à leitura; os indivíduos que sofreram TCE ligeiro que residiam em aldeias evidenciam níveis mais elevados de depressão do que aqueles que residiam em vilas; por fim, os indivíduos que sofreram traumatismo aberto revelam maiores alterações neuropsicológicas nas funções motoras e visuais, no ritmo e na aritmética comparativamente com os outros.

Pregnancy and newborns disorders followed by urine metabolomics

Chapter 1 introduces the scope of the work by identifying the clinically relevant prenatal disorders and presently available diagnostic methods. The methodology followed in this work is presented, along with a brief account of the principles of the analytical and statistical tools employed. A thorough description of the state of the art of metabolomics in prenatal research concludes the chapter, highlighting the merit of this novel strategy to identify robust disease biomarkers. The scarce use of maternal and newborn urine in previous reports enlightens the relevance of this work. Chapter 2 presents a description of all the experimental details involved in the work performed, comprising sampling, sample collection and preparation issues, data acquisition protocols and data analysis procedures. The proton Nuclear Magnetic Resonance (NMR) characterization of maternal urine composition in healthy pregnancies is presented in Chapter 3. The urinary metabolic profile characteristic of each pregnancy trimester was defined and a 21-metabolite signature found descriptive of the metabolic adaptations occurring throughout pregnancy. 8 metabolites were found, for the first time to our knowledge, to vary in connection to pregnancy, while known metabolic effects were confirmed. This chapter includes a study of the effects of non-fasting (used in this work) as a possible confounder. Chapter 4 describes the metabolomic study of 2nd trimester maternal urine for the diagnosis of fetal disorders and prediction of later-developing complications. This was achieved by applying a novel variable selection method developed in the context of this work. It was found that fetal malformations (FM) (and, specifically those of the central nervous system, CNS) and chromosomal disorders (CD) (and, specifically, trisomy 21, T21) are accompanied by changes in energy, amino acids, lipids and nucleotides metabolic pathways, with CD causing a further deregulation in sugars metabolism, urea cycle and/or creatinine biosynthesis. Multivariate analysis models´ validation revealed classification rates (CR) of 84% for FM (87%, CNS) and 85% for CD (94%, T21). For later-diagnosed preterm delivery (PTD), preeclampsia (PE) and intrauterine growth restriction (IUGR), it is found that urinary NMR profiles have early predictive value, with CRs ranging from 84% for PTD (11-20 gestational weeks, g.w., prior to diagnosis), 94% for PE (18-24 g.w. pre-diagnosis) and 94% for IUGR (2-22 g.w. pre-diagnosis). This chapter includes results obtained for an ultraperformance liquid chromatography-mass spectrometry (UPLC-MS) study of pre-PTD samples and correlation with NMR data. One possible marker was detected, although its identification was not possible. Chapter 5 relates to the NMR metabolomic study of gestational diabetes mellitus (GDM), establishing a potentially predictive urinary metabolic profile for GDM, 2-21 g.w. prior to diagnosis (CR 83%). Furthermore, the NMR spectrum was shown to carry information on individual phenotypes, able to predict future insulin treatment requirement (CR 94%). Chapter 6 describes results that demonstrate the impact of delivery mode (CR 88%) and gender (CR 76%) on newborn urinary profile. It was also found that newborn prematurity, respiratory depression, large for gestational age growth and malformations induce relevant metabolic perturbations (CR 82-92%), as well as maternal conditions, namely GDM (CR 82%) and maternal psychiatric disorders (CR 91%). Finally, the main conclusions of this thesis are presented in Chapter 7, highlighting the value of maternal or newborn urine metabolomics for pregnancy monitoring and disease prediction, towards the development of new early and non-invasive diagnostic methods.

Mitochondrial dysfunction in fatty acid β-oxidation disorders

Mitochondria are central organelles for cell survival with particular relevance in energy production and signalling, being mitochondrial fatty acid β–oxidation (FAO) one of the metabolic pathways harboured in this organelle. FAO disorders (FAOD) are among the most well studied inborn errors of metabolism, mainly due to their impact in health. Nevertheless, some questions remain unsolved, as their prevalence in certain European regions and how pathophysiological determinants combine towards the phenotype. Analysis of data from newborn screening programs from Portugal and Spain allowed the estimation of the birth prevalence of FAOD revealing that this group of disorders presents in Iberia (and particularly in Portugal) one of the highest European birth prevalence, mainly due to the high birth prevalence of medium chain acyl-CoA dehydrogenase deficiency. These results highlight the impact of this group of genetic disorders in this European region. The characterization of mitochondrial proteome, from patients fibroblasts with FAOD, namely multiple acyl-CoA dehydrogenase deficiency (MADD) and long chain acyl-CoA dehydrogenase deficiency (LCHADD), provided a global perspective of the mitochondrial proteome plasticity in these disorders and highlights the main molecular pathways involved in their pathogenesis. Severe MADD forms show an overexpression of chaperones, antioxidant enzymes (MnSOD), and apoptotic proteins. An overexpression of glycolytic enzymes, which reflects cellular adaptation to energy deficiency due to FAO blockage, was also observed. When LCHADD fibroblasts were analysed a metabolic switching to glycolysis was also observed with overexpression of apoptotic proteins and modulation of the antioxidant defence system. Severe LCHADD present increased ROS alongside with up regulation of MnSOD while moderate forms have lower ROS and down-regulation of MnSOD. This probably reflects the role of MnSOD in buffering cellular ROS, maintain them at levels that allow cells to avoid damage and start a cellular response towards survival. When ROS levels are very high cells have to overexpress MnSOD for detoxifying proposes. When severe forms of MADD were compared to moderate forms no major differences were noticed, most probably because ROS levels in moderate MADD are high enough to trigger a response similar to that observed in severe forms. Our data highlights, for the first time, the differences in the modulation of antioxidant defence among FAOD spectrum. Overall, the data reveals the main pathways modulated in FAOD and the importance of ROS levels and antioxidant defence system modulation for disease severity. These results highlight the complex interaction between phenotypic determinants in FAOD that include genetic, epigenetic and environmental factors. The development of future better treatment approaches is dependent on the knowledge on how all these determinants interact towards phenotype.!