Dissertation (Ph.D.)--University of South Florida, 2008. / Title from PDF of title page. Document formatted into pages; contains 98 pages. Includes vita. Includes bibliographical references.

A doença hepática associada a sobrecarga de ferro pode ocorrer devido a causas genéticas ou secundárias. Esse estudo avaliou pacientes com hepatopatia crônica com sobrecarga de ferro submetidos à pesquisa das mutações HFE no período de 2007-2009 e classificou como portadores de hemocromatose hereditária HFE (HH-HFE) aqueles que apresentavam as mutações C282Y/C282Y ou C282Y/H63D e como sobrecarga de ferro não HFE aqueles que apresentavam outras mutações no gene HFE como C282Y/-, H63D/- e H63D/H63D ou pacientes sem qualquer uma dessas mutações mencionadas. Os objetivos do estudo foram 1) analisar e correlacionar os aspectos fenotípicos e genotípicos de grupo de indivíduos com doença hepática crônica e sobrecarga de ferro; 2) caracterizar o quadro clínico, laboratorial e anatomopatológico, em busca de achados compatíveis com o fenótipo de hemocromatose; 3) Correlacionar o quadro clínico com as mutações no gene HFE. Foram analisados 108 indivíduos portadores de hepatopatia crônica selecionados a partir de saturação de transferrina (ST) > 45% e ferritina sérica > 350 ng/mL. Foram estudados e comparados 16 pacientes no grupo HH-HFE com 92 no grupo sobrecarga de ferro não HFE. Da casuística geral, a idade média ao diagnóstico da doença foi de 46,69 anos (16-77), com 70,73% constituída por indivíduos de cor branca, 77,57% do sexo masculino e 64,8% tinham cirrose hepática. A frequência de cirrose hepática não diferiu entre os grupos, entretanto, artropatia, carcinoma hepatocelular, diabetes e osteoporose foram mais frequentes no grupo HH- HFE (53,8% x 15,9%, 31,2% x 7,06%, 56,2% x 30%, 72,7% x 32,1%, respectivamente, p < 0,05). Os pacientes com mutações HFE diagnósticas de HH apresentaram maior chance de ter carcinoma hepatocelular (OR= 5,0, p= 0,032) quando comparados com os portadores de outros genótipos HFE e aqueles sem mutação. Os níveis de ST, ferro e ferritina também foram maiores naquele grupo, bem como os graus de siderose 3 e 4 (p= 0,026). A ST foi a variável que se correlacionou independentemente com o diagnóstico das mutações C282Y/C282Y e C282Y/H63D. A frequência de fatores de risco para sobrecarga de ferro não diferiu entre os grupos. Observou-se, entretanto, que no grupo HH-HFE havia maior número de pacientes sem qualquer fator de risco detectado (p= 0,019). Níveis de ST > 82% apresentaram maior valor preditivo negativo para o diagnóstico de HH-HFE do que os de ferritina, ferro, capacidade total de ligação de ferro e de transferrina. Concluímos que os portadores de HH-HFE têm maiores graus de sobrecarga de ferro quando comparados ao grupo de sobrecarga de ferro não-HFE; em indivíduos com doença hepática crônica. ST > 82% tem maior acurácia para diagnóstico de HH-HFE; portadores de mutações C282Y em homozigose ou em heterozigose composta com H63D têm maior chance de apresentar carcinoma hepatocelular do que os portadores de outras mutações no gene HFE e pacientes sem mutação / Chronic liver disease related to iron overload may occur due to genetic or secondary causes. This study analyzed patients with chronic liver diseases and iron overload who were tested for HFE mutations from 2007 to 2009. Patients with C282Y/C282Y or C282Y/H63D mutations were diagnosed with HFE hereditary hemochromatosis (HFE-HH) and those with other HFE genotypes (C282Y/-, H63D/- or H63D/H63D) or individuals without HFE mutations (wild type) were designed as non-HFE iron overload. The aims of this study were: 1) to analyze and to establish correlations between phenotypic and genotypic aspects of individuals with chronic liver disease and with iron overload; 2) to charachterize the clinical manifestations, laboratory and histological findings consistent with the phenotype of hemochromatosis; 3) to verify associations between clinical manifestations and HFE mutations. One hundred and eight patients with chronic liver diseases and with iron overload, defined as transferrin saturation (TS) > 45% and serum ferritin levels > 350 ng/mL were included. Sixteen patients had HH-HFE and were compared with 92 patients with non-HFE iron overload group. The average of age at diagnosis was 46.69 years (16-77), 70.73% were Caucasians, 77.57% were male and 64.8% had hepatic cirrhosis. The proportion of hepatic cirrhosis was similar in both groups, nevertheless arthropathy, hepatocellular carcinoma, diabetes and osteoporosis were more frequent in the HFE-HH group (53,8% x 15,9%, 31,2% x 7,06%, 56,2% x 30%, 72,7% x 32,1%, respectively, p < 0,05). The HFE C282Y/C282Y or C282Y/ H63D genotypes had a higher chance to develop hepatocellular carcinoma (OR= 5.0, p= 0.032) when compared with the other HFE genotypes and with those wild type. The levels of TS, serum iron and ferritin were greater in HFE-HH group, as well as hepatic siderosis grade 3 and 4 (p= 0.026). TS was the biochemical marker of iron overload with the higher independent correlation with the presence of C282Y/C282Y and C282Y/H63D mutations. The frequency of risk factors for iron overload was not different between the groups, however, in HFE-HH group a greater number of patients without any risk factor was detected (p= 0.019). TS > 82% had a higher predictive negative value for diagnosing HFE-HH when compared to the levels of ferritin, serum iron, total iron binding capacity and transferrin. We concluded that the HFE-HH patients had a greater iron overload than patients with chronic liver diseases with non-HFE iron overload. TS > 82% had more accuracy to diagnose HFE-HH. The carriers of C282Y/C282Y or C282Y/H63D mutations had a higher probability to develop hepatocellular carcinoma, when compared to the patients with HFE genotypes and patients wild type

Atualmente, muitas são as diretrizes na literatura quanto à influência do Helicobacter pylori na Doença do Refluxo Gastroesofágico. Alguns autores acreditam que o H. pylori poderia ter um efeito protetor para o desenvolvimento na DRGE e outros até mesmo concluem que o agente possa ser um fator agravante na doença. Muitas publicações nos alertam para o desenvolvimento de sintomas da DRGE, ou mesmo da esofagite, em uma porcentagem razoável de pacientes erradicados pelo esquema tríplice para tratar o H. pylori, sendo que aproximadamente 10% teriam DRGE. Na verdade, por essas dúvidas, ainda não foi estabelecido um consenso quanto à importância do H. pylori na etiopatogenia da DRGE e suas complicações. Fato também discutido, seria a importância das cepas para a formação da esofagite em pacientes submetidos à erradicação. Talvez as mais virulentas, assim como a presença da “ilha de patogenicidade”(cagA) ou algumas cepas vacuolizantes (vacA), teriam uma maior relação com a prevenção da esofagite. Outro mecanismo importante, apontado por muitos, para a formação da esofagite em pacientes erradicados seria a elevação do índice de Massa Corpórea nesse grupo de pacientes erradicados associados ou não à presença da hérnia hiatal e justificados pela melhor qualidade de vida após melhora dos sintomas depois da erradicação. Em nosso estudo, 148 pacientes com úlcera péptica ativa ou cicatrizada receberam esquema tríplice de erradicação para o Helicobacter pylori e foram submetidos a exame endoscópico e ao teste histopatológico das amostras colhidas por biópsias de corpo e antro, teste respiratório com Carbono 14 e urease, antes e após o tratamento. Realizamos a genotipagem do agente, através do PCR, separando amostras de corpo e de antro, para determinar as cepas do agente. Os pacientes foram seguidos ambulatorialmente por um ano e avaliados quanto à melhora ou piora dos sintomas relacionados a DRGE (pirose) e sintomas considerados inespecíficos como a dor epigástrica; também procuramos quantificar o ganho ou perda do IMC. Encontramos 28 pacientes (18,9%) com esofagite erosiva (24 grau A e 4 grau B de Los Angeles) endoscópica após o tratamento do agente. Deste grupo, somente 3 pacientes que não tinham sintomas desenvolveram pirose (2%). A grande maioria dos pacientes se beneficiou com o tratamento, mostrando que 69 46,6%) melhoraram da pirose e outra grande maioria melhorou dos sintomas inespecíficos. Em 18 pacientes ulcerosos com esofagite, a análise de fragmentos de corpo foi cagA positiva (64,3%) e em amostras de antro 21 eram cagA positivos (75%). Assim como no grupo geral, as cepas vacuolizantes s1b/m1 e s1b foram, respectivamente, as mais encontradas no grupo da esofagite endoscópica. Houve ligeiro aumento nos Índices de Massa Corpórea em pacientes com e sem esofagite, sendo estatisticamente mais significativo nos 120 pacientes sem esofagite. Apesar do aparecimento da esofagite erosiva endoscópica em número razoável de pacientes, a sintomatologia não foi fator determinante, pois muitos melhoraram dos sintomas após o tratamento, e a erradicação não foi importante para determinar o grau de esofagite erosiva. Não foi encontrada nenhuma relação entre a genotipagem do agente e o desenvolvimento de esofagite endoscópica. O aumento de IMC, também não justifica, em nosso estudo a esofagite em pacientes ulcerosos tratados contra o H. pylori. / Nowadays, there are many directrixes in literature as to the influence of Helicobacter pylori, in the Disease of Gastroesophagic reflux. Some authors believe that H. pylori could have a protective effect to the development of GERD, and others even conclude that the agent may be an aggravating factor in the disease. Many publications allert us to the development of symptoms of GERD, or even the esophagitis,in a reasonable percentage of erradicated patients by the triplicit scheme to treat H. pylori, and 10%, approximately, would have GERD. In fact, due to these doubts, a consensus has not been established yet to the importance of H. pylori in the GERD’s etiopathogenic and its complications. The strains importance to the formation of esophagitis in patients submitted to erradication is another fact that has also been discussed. Maybe the most virulent ones, as the presence of “pathogenical island”(cagA) or some other vacuolating cytotoxin (vacA), would have a larger relation in the esophagitis prevention. Another important mechanism, pointed by many, to the formation of esophagitis in erradicated patients would be the elevation of Body Mass Index in this group of eradicated patients associated or not to the presence of hiatal hernia and justified by a better quality of life due to symptoms’ improvement after erradication. In our studies, 148 patients with active or healed peptic ulcer received triplicit scheme of erradication to the Helicobacter pylori and were submitted to endoscopic exams and histopathologic test of gathered samples by body and antro biopsies, respiratory test with carbon 14 and ureasis, before and after treatment. We have done the agent genotyping, through the PCR, separating samples of body and antro, to determine the agent Cepas. The patients have been followed ambulatorially for a year and evaluated as to the improvement or worsening of the symptoms related to GERD (pyrosis) and symptoms considered non-specific as epigastric pain; we have also tried to quantify the gain or loss of Body Mass Index. We found 28 patients(18.9%) with endoscopic erosive esophagitis (24 degree A and 4 degree B of Los Angeles) after agent’s treatment. In this group, only three patients who had no symptoms developed pyrosis (2%). Most of the patients benefitted from treatment showing that 69 (46.6%) presented improvement in pyrosis and another great majority improved non-specific symptoms. In 18 ulcered patients with esophagitis, the body analysis fragments was positive cagA (64.3%)and in antro samples of 21 were positive cagA (75%). As in the general group, the vacuolizing cepas slb/ml and slb were, respectivelly, the most found in the endoscopic esophagitis group. There was a slight raise in the BMI in patients with and without esophagitis, and it is, statistically more meaningful in the 120 patients without esophagitis. Even though there was the appearance of endoscopic erosive esophagitis in a reasonable number of patients, the symptmology was not a determining factor, because many have got better after the treatment, and erradication was not important to determine the erosive esophagitis. It was not found any relation between the agent genotyping and the development of endoscopic esophagitis. The raise of BMI does not justify in our study the esophagitis in ulcered patients treated against H. pylori.

Indiana University-Purdue University Indianapolis (IUPUI) / Prospective epidemiologic evidence indicates that both stressful life events (SLEs) and depression are associated with an increased risk of subclinical atherosclerosis and cardiovascular disease (CVD) events. Even though stressful life events (SLEs) and depression co-occur and may act together to influence cardiovascular disease (CVD) risk, these psychosocial factors have been mainly examined in isolation. For instance, depression may moderate the relationship between SLEs and CVD outcomes. I hypothesized that depressive symptoms would potentiate the deleterious effect of SLEs on subclinical atherosclerosis. This hypothesis is plausible, given that depressed adults exhibit exaggerated and prolonged sympathetic nervous system, hypothalamic-pituitary-adrenal (HPA) axis, and inflammatory responses to stress, which in turn could promote atherosclerosis. As compared to their nondepressed counterparts, depressed individuals may also be more likely to engage in maladaptive methods to cope with SLEs (e.g., increased tobacco use, alcohol use, and consumption of low-nutrient, energy dense foods), which could also promote atherosclerosis. I examined cross-sectional data from 274 to 279 (depending on the outcome measure) older, African American adults (mean age = 66 years, 67% female) with no evidence of clinical CVD or dementia who participated in the St. Louis African American Health-Heart study (2009–2011). Number of SLEs was assessed using the Life Events Calendar, a structured interview. From this interview, a continuous SLEs variable was computed (number of adult SLEs: 0, 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, or 11+). Severity of depression symptoms was measured using the 17-item Hamilton Rating Scale for Depression (HAM-D). Two measures of subclinical atherosclerosis were obtained: carotid intima-media thickness (CIMT; assessed by ultrasonography) and coronary artery calcification (CAC; assessed by multi-detector computerized tomography). I conducted linear (CIMT) and logistic (CAC) regression models, first adjusted for demographics (age, sex, education) and then fully-adjusted (demographics; mean arterial pressure; low density lipoprotein cholesterol (LDL-C), high density lipoprotein cholesterol (HDL-C); hemoglobin A1c; BMI; tobacco use; diabetes diagnosis; and use of antihypertensitve, lipid lowering, antidiabetic, and antidepressant medications). No main effects of SLEs or HAM-D were found for CIMT or CAC. There were also no SLEs by HAM-D interactions for CIMT or CAC. Because the current results are largely inconsistent with prior literature and there is a paucity of studies utilizing African American samples, future research is needed to examine the independent and interactive associations of SLEs and depressive symptoms with measures of subclinical atherosclerosis. If the present results are replicated, it may suggest that SLEs, depressive symptoms, and their interactive effect are not cardiotoxic among African American adults.

No description available.

Diabetes is a rapidly growing disease with 415 million affected adults worldwide. The pancreatic endocrine cells, most importantly the insulin producing β-cells, play an important role in regulating blood glucose homeostasis. Type 1 diabetes (T1D) is characterized by the inability of the pancreas to secrete sufficient amounts of insulin due to autoimmune destruction of insulin producing β-cells. Type 2 diabetes (T2D) on the other hand is characterized by defects in insulin secretion and insulin sensitivity. Alterations in the β-cell mass (BCM) and/or function play a major role in the development and progression of the disease. Understanding BCM dynamics in disease models is therefore a key aspect for better interpretation of research results. In this thesis, we have used optical projection tomography (OPT) as a tool to evaluate a non-invasive imaging modality for β-cell scoring and to study disease dynamics in frequently used animal models for T1D and T2D. The possibility to monitor BCM in vivo would radically improve our competence in studying the pathogenesis of diabetes and in therapeutic interventions. Single photon emission computed tomography (SPECT) is a widely used technique that has become a promising approach to monitor changes in BCM in vivo. A key issue for using this approach is to evaluate the β-cell specificity and read out of the utilized radiotracers. This is most commonly performed by conventional stereological approaches, which rely on the extrapolation of 2D data. We developed a protocol for SPECT-OPT multimodal imaging that enables rapid and accurate cross evaluation of SPECT based assessments of BCM. While histological determination of islet spatial distribution was challenging, SPECT and OPT revealed similar distribution patterns of the radiotracer 111In-exendin-3 and insulin positive β-cell volumes respectively between different pancreatic lobes, both visually and quantitatively. We propose SPECT-OPT multimodal imaging as an accurate and better approach for validating the performance of β-cell radiotracers. The leptin deficient ob/ob mouse is a widely used model for studies of metabolic disturbances leading to T2D, including obesity and insulin resistance. By OPT imaging we created the first 3D-spatial and quantitative account of BCM distribution in this model. We observed a previously unreported degree of cystic lesions in hypertrophic islets, that were occupied by red blood cells (RBCs) and/or fibrin mesh. We propose that these lesions are formed by a mechanism involving the extravasation of RBCs/plasma due to increased blood flow and islet vessel instability. Further, our data indicate that the primary lobular compartments of the ob/ob pancreas have different potentials for expanding their β-cell population. Unawareness of these characteristics of β-cell expansion in ob/ob mice presented in this study may significantly influence ex vivo and in vivo assessments of this model in studies of β-cell adaptation and function. The tomographic data, on which this study was based, will be made publically available as a resource to the research community for the planning and interpretation of research involving this model. There are limited studies on early metabolic and functional changes of BCM in the settings of T1D. In order to assess initial metabolic alterations in BCM before the onset of diabetes, we characterized congenic diabetes prone Bio-breeding (BB) DR.lyp/lyp rats, a widely used model for T1D diabetes. We observed lower acute insulin response, reduced islet blood flow and a significant reduction in the BCM of small and medium sized islets at a very early stage (40 days), i.e. before insulitis and development of diabetes. Underlying changes in islet function may be a previously unrecognized factor of importance in the development of T1D.

The AKR strain of mice have a genetic trait for spontaneous development of lymphocytic leukemia. In this study, leukemic mice were found to have significantly larger (p<0.01) thymuses and spleens than preleukemic mice. The enlarged leukemic tissues were densely packed with a light staining cell, with a hollow-appearing nucleus. Tissues from preleukemic mice were observed to be infiltrated with a smaller, darker-staining lymphocyte. Fluorescent antibody staining was done on preleukemic and leukemic tissues, using three antisera against murine lymphocyte theta antigen, and an antiserum against murine IgG. Significantly brighter fluorescence, (p <0.05) with theta-specific antisera, was found in leukemic thymuses,spleens, and kidneys than in the same preleukemic tissues. Leukemic tissues had significantly brighter fluorescence (p <0.05) than preleukemic tissues with IgG antiserum.

M.A. / The study aims to determine whether statistically significant differences exist between boys with attention deficit hyperactivity disorder (ADHD) and boys without ADHD with regard to hemispheric language lateralization and the laterality of various modalities (handedness, eyedness and footedness). According to the literature, a possible connection exists between abnormal lateralization patterns and various developmental disorders (Corballis, 1983; Geschwind & Behan, 1982; Hiscock, 1988, McFarland, 1981; Turkewitz, 1988). Lateralization in the current study refers to hemispheric language specialisation, hand dominance, foot dominance and eye dominance. In most people these functions are lateralized to the one side of the body by the age of seven (Kalat, 1995; Kolb & Whishaw, 1996). They typically manifest a dominant left hemisphere for language and a right-sided dominance for handedness, footedness and eyedness. The result is a dominant left hemisphere, due to the left side of the brain controlling the right side of the body. Some children however manifest insufficient or poor lateralization of these functions. For purposes of this study, it would imply that the functions of language specialisation, handedness, footedness and eyedness are not all lateralized to one side of the body. A possible connection between this poor or insufficient lateralization and ADHD might exist. According to the DSM IV (1997) the essential feature of ADHD is a persistent pattern of inattention and/or hyperactivity/impulsivity that is more frequent and severe than is typically observed in individuals at a comparable level of development. Some of these symptoms causing impairment must have been present before age seven, although many individuals are only diagnosed after the symptoms have been present for a number of years. Impairment resulting from the symptoms should be present in at least two settings, for example, at school and at home. Clear evidence must exist of interference with developmentally appropriate social, academic, or occupational functioning. An empirical study was conducted in order to compare the hemispheric language specialisation, handedness, eyedness and footedness of the various subjects. The subjects consisted of 20 ADHD boys (8 -12 years) who met the criteria of the DSM IV and 20 Non-ADHD boys (8-12 years) without any learning problems. Various interference variables were controlled in the selection of the subjects (see section 5.2.3) Kimura's dichotic listening technique was used to measure hemispheric language specialisation and the Harris-test for Lateral Dominance was used to measure handedness, eyedness and footedness. Wilks's lambda, Pearson's chi-quadrant and Student's t-tests were used during statistical analysis of data. Results indicated statistically significant differences between ADHD boys and non-ADHD boys with regard to hemispheric language specialisation, handedness and footedness. Overall, the results indicated that the ADHD boys are not as strongly lateralized as the non-ADHD boys. The non-ADHD boys showed a stronger left hemispheric language specialisation, right hand dominance and right foot dominance. No statistical differences were recorded with regard to eyedness. The current study provides possible theoretical support for the theory that a connection exists between poor or insufficient lateralization patterns and children with ADHD. However, the study only focused on white boys between the ages of 8-12 years. Further studies involving different age groups, cultures and gender are recommended.

O efeito anti-aterogênico da HDL foi sugerido ser devido, parcialmente, à ação da paraoxonase (PON) associada à HDL. Três SNPs em PON1 (L55M e Q192R) e PON2 (S311C) têm sido implicados como fatores de risco independentes para doença arterial coronariana (DAC) em alguns, mas não todos os estudos. O efeito destes três polimorfismos do gene PON na DAC e na concentração sérica de lipídios, apolipoproteínas A-I e B (apo A-I e apo B) foi investigado em 221 indivíduos sem vínculos genéticos. Os três polimorfismos genéticos (L55M, Q192R e S311C) do gene PON foram analisados por PCR-RFLP. Não houve diferença entre a distribuição genotípica e a freqüência relativa dos alelos dos polimorfismos L55M, Q192R e S311C do gene PON entre pacientes e controles. Não houve associação entre os polimorfismos da PON e a DAC na população estudada. As freqüências dos haplótipos dos pacientes foram similares às encontradas no grupo controle. O polimorfismo L55M do gene PON1 está associado com variações na concentração sérica de apo A-I dos pacientes. O polimorfismo S311C do gene PON2 não está associado com variações na concentração sérica de lipídios, apo A-I e apo B dos pacientes. / The anti-atherogtenic effect of the HDL has been suggested to be due, partially, to the action of the HDL-associated paroxonase(PON). Three SNPs in PON1 (L55M e Q192R) and PON2 (S311C) have been involved as independent risk factors for coronary artery disease (CAD), in some, but not all studies. The effect of these three polymorphisms of the PON gene on CAD and on the levei of lipids, apolipoproteins A-I e B (apo A1 and apo B) was investigated in 221 genetically unrelated individuais. The three gene polymorphismis (L55M, Q192R e S311C) of the PON gene were analyzed by PCR-RFLP. Is no significant difference between distribuition of genotype and allele frequencies of the L55M, Q192R and S311C polymorfisms of the PON gene between patient group and controls. Is no association between polymorphisms of the PON gene and CAD in the population studied. The frequencies of the haplotypes in the patients were similar to those found in the control group. The L55M polymorphism of the PON1 gene is associated with variations of the level of polipoprotein A-I at patients. The S311C polymorphism of the PON2 is not associated with variations of the level of lipids, apo A-I and apo B at patients.

Em outubro de 2005 a notificação de 17 casos de doença ocular de etiologia desconhecida, envolvendo, em sua maioria, a população infantil da cidade de Araguatins/TO, levou as autoridades locais a pedirem ajuda a Secretaria de Estado da Saúde do Estado do Tocantins no intuito de descobrirem sua etiologia, tratamento e prevenção. Nos pacientes acometidos, os sinais freqüentemente observados foram: intensa hiperemia conjutival, granuloma, episclerite, infiltrado corneano periférico. Na anamnese realizada nos pacientes foi observado que todos tiveram contato com as águas do Rio Araguaia. Os resultados obtidos a partir do processamento das amostras de água, sedimentos e substratos particularmente na vegetação marginal inundada, permitiram confirmar a hipótese de que deveria haver uma fauna rica de esponjas no Araguaia, no trecho fronteiro à cidade de Araguatins A presença intraocular de espícula de esponja de água doce das espécies Drulia uruguayensis e Oncosclera navicela foi confirmada em material avaliado histopatologicamente proveniente de três pacientes que haviam sido submetidos a lensectomia, sugerindo que espículas de água doce poderiam ser um surpreendente novo agente etiológico de patologia ocular. Assim, neste estudo foram realizados ensaios de citotoxicidade com amostras de duas espécies de esponjas coletadas no local. Os resultados indicam que os extratos das esponjas após filtração em filtro Millipore 0,45 &mu;m continuaram apresentando atividade citotóxica, sugerindo haver um componente SOLÚVEL, e não somente espículas, capaz de induzir morte celular na população de células utilizadas. Os indivíduos acometidos foram na maioria do sexo masculino com idade entre 05 e 14 anos. / In October 2005 the notification of 17 cases of eyes disease of unknown etiology, involving, in its majority, the infant population of the city of Araguatins/TO, led the local authorities to ask help to the Secretariate of State of Health of the State of Tocantins in order to discover their etiology, treatment and prevention. In affected patients, the signs frequently observed were: intense hyperemia conjutival, granuloma, episclerite, peripheral cornea infiltrated. In the anamnesis performed in patients was observed that all of them had contact with the waters of the Araguaia river. The results obtained from processing samples of water, sediments and substrates particularly in the vegetation marginal flooded, allowed confirming the hypothesis that there should be a rich fauna sponges in Araguaia, close to the city of Araguatins The presence of spicula of intraocular sponge species of freshwater Drulia uruguayensis and Oncosclera navicela was confirmed in material evaluated histopathologically from three patients who had undergone lensectomy, suggesting that \"spikes freshwater could be a surprising new etiologic agent of pathology ocular\". Thus, in this study was performed cytotoxicity assays with samples from two species of sponges collected in place. The results indicate that the extracts of sponges after filtration Millipore 0.45 &mu;m continued presenting cytotoxic activity, suggesting there is a SOLUBLE component, and not only spikes, capable of inducing cellular death in the population of cells used. The individuals affected were the majority of males aged between 05 and 14 years.