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1.
Chemistry ; 29(24): e202203990, 2023 Apr 25.
Article in English | MEDLINE | ID: mdl-36734519

ABSTRACT

A combined experimental and theoretical study has been carried out on 4-fluoro-threonine, the only naturally occurring fluorinated amino acid. Fluorination of the methyl group significantly increases the conformational complexity with respect to the parent amino acid threonine. The conformational landscape has been characterized in great detail, with special attention given to the inter-conversion pathways between different conformers. This led to the identification of 13 stable low-energy minima. The equilibrium population of so many conformers produces a very complicated and congested rotational spectrum that could be assigned through a strategy that combines several levels of quantum chemical calculations with the principles of machine learning. Twelve conformers out of 13 could be experimentally characterized. The results obtained from the analysis of the intra-molecular interactions can be exploited to accurately model fluorine-substitution effects in biomolecules.

2.
Eur Arch Otorhinolaryngol ; 278(3): 781-789, 2021 Mar.
Article in English | MEDLINE | ID: mdl-32656673

ABSTRACT

PURPOSE: The need for prolonged invasive mechanical ventilation in COVID-19 patients is placing the otorhinolaryngologist in front of an increasing request for tracheostomy. Nowadays, there is uncertainty regarding the timing of tracheostomy, the prognosis of these patients and the safety of healthcare workers. The aim of this study is to evaluate the efficacy and safety of tracheostomy placement in patients with COVID-19. METHODS: A retrospective cohort study on 23 COVID 19 patients, to analyse the timing of tracheostomy, the risk factors associated with in-hospital death and the infection of the involved health care workers. Early tracheostomy was defined as ≤ 10 days and late ones > 10 days. RESULTS: The mortality rate of COVID-19 patients admitted to ICU that underwent tracheostomy was 18%. The overall mortality of patients admitted to ICU was 53%. The univariate analysis revealed that early tracheostomy, SOFA score > 6, and D-dimer level > 4 were significantly associated with a greater risk of death. At the multivariate analysis SOFA score > 6 and D-dimer level > 4 resulted as significant factors for a higher risk of death. No health care workers associated with tracheostomy are confirmed to be infected by SARS-CoV2. CONCLUSION: We suggest to wait at least 14 days to perform tracheostomy. In patients with SOFA score > 6 and D dimer > 4, tracheostomy should not be performed or should be postponed. Optimized procedures and enhanced personal protective equipment can make the tracheostomy safe and beneficial in COVID-19 patients.


Subject(s)
COVID-19 , Tracheostomy , Adult , Aged , Aged, 80 and over , Disease Outbreaks , Female , Humans , Italy/epidemiology , Male , Middle Aged , RNA, Viral , Respiration, Artificial , Retrospective Studies , SARS-CoV-2
3.
Nutr Metab Cardiovasc Dis ; 20(10): 727-33, 2010 Dec.
Article in English | MEDLINE | ID: mdl-19822409

ABSTRACT

BACKGROUND AND AIMS: A blood glucose (BG) fall after an oral glucose load has never been described previously at a population level. This study was aimed at looking for a plasma glucose trend after an oral glucose load for possible blood glucose fall if any, and for its impact on coronary mortality at a population level. METHODS AND RESULTS: In subjects from an unselected general population, BG and insulin were detected before and 1 and 2h after a 75-g oral glucose load for insulin sensitivity and ß-cell function determination. Blood pressure, blood examinations and left ventricular mass were measured, and mortality was monitored for 18.8±7.7 years. According to discriminant analysis, the population was stratified into cluster 0 (1-h BG < fasting BG; n=497) and cluster 1 (1-h BG ≥ fasting BG; n=1733). To avoid any interference of age and sex, statistical analysis was limited to two age-gender-matched cohorts of 490 subjects from each cluster (n=940). Subjects in cluster 0 showed significantly higher insulin sensitivity and ß-cell function, lower visceral adiposity and lower blood pressure values. Adjusted coronary mortality was 8 times lower in cluster 0 than 1 (p<0.001). The relative risk of belonging to cluster 1 was 5.40 (95% CI 2.22-13.1). CONCLUSION: It seems that two clusters exist in the general population with respect to their response to an oral glucose load, independent of age and gender. Subjects who respond with a BG decrease could represent a privileged sub-population, where insulin sensitivity and ß-cell function are better, some risk factors are less prevalent, and coronary mortality is lower.


Subject(s)
Blood Glucose/metabolism , Glycemic Index , Insulin/blood , Adult , Aged , Aged, 80 and over , Analysis of Variance , Blood Pressure , Cluster Analysis , Coronary Disease/mortality , Coronary Disease/prevention & control , Female , Follow-Up Studies , Glucose Tolerance Test , Humans , Insulin Resistance , Male , Metabolic Syndrome/complications , Middle Aged , Obesity/complications , Risk Factors , Young Adult
4.
Ann N Y Acad Sci ; 1051: 148-55, 2005 Jun.
Article in English | MEDLINE | ID: mdl-16126954

ABSTRACT

Antibodies to gangliosides and Purkinje cells have been reported in patients with celiac disease (CD) with neuropathy and ataxia, respectively. Whether these antibodies are pathogenic is not clear. The response of neurological symptoms and antibody titers to a gluten-free diet is still controversial. The objective of our study was to assess whether neurological manifestations in CD patients correlate with antibody titers and a gluten-free diet.Thirty-five CD patients (9 males, 26 females, mean age 37.1 +/- 12.6 yrs) were followed prospectively. At initial evaluation, 23 were on a gluten-free diet, 12 were not. At recruitment and during follow-up, patients underwent neurological and electrophysiological evaluation. IgG, IgM, and IgA anti-ganglioside antibodies were assayed by ELISA; anti-neuronal antibodies were assessed by immunohistochemistry and Western blot. Four patients, all males, had electrophysiological evidence of neuropathy; three had been on a gluten-free diet for several months, and one was newly diagnosed. One had reduced tendon reflexes; another complained of distal paresthesias. With regard to anti-ganglioside antibodies, three patients had a moderate increase in antibodies without symptoms or signs of neuropathy. No patients had ataxia or cerebellar dysfunction, although in four patients reactivity to neuronal antigens was found. In 17 patients, an electrophysiological follow-up (mean duration of follow-up, 9 months) showed no changes. In conclusion, the preliminary results of this prospective study indicate that neuropathy, usually subclinical, may accompany CD. Antibody titers do not seem to correlate with neurological symptoms/signs or diet. Ongoing follow-up will help confirm these data and clarify the role, if any, of antibodies in neurological involvement in CD.


Subject(s)
Autoimmunity , Celiac Disease/complications , Gangliosides/immunology , Nervous System Diseases/etiology , Neurons/immunology , Adult , Celiac Disease/immunology , Celiac Disease/physiopathology , Female , Glutens/adverse effects , Humans , Male , Middle Aged , Prospective Studies
5.
Minerva Chir ; 59(3): 301-5, 2004 Jun.
Article in English | MEDLINE | ID: mdl-15252398

ABSTRACT

Colonic diverticular disease is a benign condition typical of the Western world, but it is not rare for even the 1st episode of diverticulitis to carry potentially fatal complications. The evolution of a peridiverticular process generally poses problems for medical treatment and exposes patients to repeated episodes of diverticulitis, making surgical treatment necessary in approximately 30% of symptomatic patients. One of the most worrying complications of diverticulosis is internal fistula. The most common types of fistula are colovesical and colovaginal, against which the uterus can act as an important protective factor. The symptoms and the clinical and instrumental management of patients with diverticular fistulas are much the same as for patients with episodes of acute diverticulitis. Staging of the disease (according to Hinchey) should be done promptly so that the necessary action can be taken prior to surgery, implementing total parenteral nutrition (TPN), nasogastric aspiration and broad-spectrum antibiotic treatment. The best surgical approach to adopt in patients with diverticulitis complicated by fistula is still not entirely clear, though the 3-step strategy is currently tending to be abandoned due to its high morbidity and mortality rates. There is a widespread conviction, however, that the 2-step strategy (Hartmann, or resection with protective stomy) and the 1-step alternative should be reserved, respectively, for patients in Hinchey stages 3, 4 and 1, 2 with a situation of attenuated local inflammation. The 1-step approach seems to be safe and effective. This report describes a case of colovaginal fistula in a patient with colonic diverticulosis who had recently undergone hysterectomy, but who, unlike such cases in the past, was treated in a single step using a laparoscopic technique.


Subject(s)
Colonic Diseases/surgery , Diverticulum/surgery , Intestinal Fistula/surgery , Laparoscopy , Vaginal Fistula/surgery , Colonic Diseases/complications , Colonic Diseases/diagnostic imaging , Diverticulitis/surgery , Diverticulum/complications , Diverticulum/diagnostic imaging , Female , Humans , Hysterectomy, Vaginal/adverse effects , Intestinal Fistula/diagnostic imaging , Intestinal Fistula/etiology , Middle Aged , Radiography , Sigmoid Diseases/diagnostic imaging , Sigmoid Diseases/etiology , Sigmoid Diseases/surgery , Treatment Outcome , Vaginal Fistula/diagnostic imaging , Vaginal Fistula/etiology
6.
Dig Liver Dis ; 36(5): 337-41, 2004 May.
Article in English | MEDLINE | ID: mdl-15191203

ABSTRACT

UNLABELLED: Coeliac disease is an autoimmune enteropathy characterized by an enhanced permeability of the intestinal epithelial barrier. In epithelial cells paracellular permeability is regulated by intercellular tight junction. The cytoplasmic protein ZO-1 interacts directly with F-actin and plays a pivotal role in the structural and functional organization of tight junction. AIM: The aim of this study was to investigate the expression and localization of ZO-1 in the intestinal mucosa of coeliac patients. PATIENTS AND METHODS: Twenty patients with active coeliac disease, seven of whom underwent a repeat biopsy following a gluten-free diet and 27 control subjects, were studied. In all subjects, three biopsies were obtained from distal duodenum during upper gastrointestinal endoscopy. ZO-1 protein localization and levels were detected by immunofluorescence followed by confocal microscopy analysis and immunoblotting. ZO-1 mRNA expression was assessed by RT-PCR. F-actin distribution was also investigated. RESULTS: In patients with active coeliac disease, both ZO-1 protein levels and mRNA were clearly reduced. Cytoskeletal organization was disrupted with F-actin staining concentrated at the subcortical and basal surface regions. Abnormalities in ZO-1 expression and actin organization were reversed after a gluten-free diet. CONCLUSIONS: In active coeliac disease, ZO-1 protein expression is downregulated at the transcriptional level in association with F-actin redistribution. These changes are completely reversed after a gluten-free diet and could contribute to the increased intestinal paracellular permeability observed in this disorder.


Subject(s)
Celiac Disease/diet therapy , Celiac Disease/metabolism , Down-Regulation , Membrane Proteins/metabolism , Phosphoproteins/metabolism , Transcription, Genetic , Actins/metabolism , Adolescent , Adult , Blotting, Western , Case-Control Studies , Celiac Disease/genetics , Child , Diet, Protein-Restricted , Duodenum/metabolism , Duodenum/pathology , Female , Fluorescent Antibody Technique , Humans , Intestinal Mucosa/metabolism , Intestinal Mucosa/pathology , Male , Membrane Proteins/genetics , Microscopy, Confocal , Middle Aged , Phosphoproteins/genetics , RNA, Messenger/metabolism , Reverse Transcriptase Polymerase Chain Reaction , Zonula Occludens-1 Protein
7.
Clin Exp Allergy ; 31(11): 1771-8, 2001 Nov.
Article in English | MEDLINE | ID: mdl-11696054

ABSTRACT

BACKGROUND: The involvement of IgE-mediated hypersensitivity reactions in the genesis of gastrointestinal symptoms after ingestion of foods containing wheat has been rarely reported. OBJECTIVE: To detect IgE specifically binding to wheat proteins in the sera of atopic and non-atopic patients suffering from gastrointestinal symptoms after ingestion of wheat and to evaluate the reliability of skin prick test and CAP in the diagnosis of food allergy to wheat. METHODS: The sera of patients (10 atopic and 10 non-atopic) previously diagnosed as suffering from irritable bowel syndrome and complaining of symptoms after wheat ingestion were analysed by immunoblotting for IgE binding to water/salt-soluble and insoluble wheat flour proteins. RESULTS: All the atopic patients and only one of the non-atopic patients were positive to wheat CAP. For the patients tested, skin prick test was positive for all the atopic patients and for only one of the non-atopic patients. However, immunoblotting experiments showed the presence of specific IgE to wheat proteins in all the patients. Ten out of 11 of the wheat CAP-positive patients had IgE binding to a soluble 16-kDa band, but the same band was recognized, in a slighter way, by only two out of nine of the wheat CAP-negative patients. Moreover, although almost all of the patients were negative in CAP testing with gluten, 19 out of 20 recognized protein bands belonging to the prolamin fraction. CONCLUSIONS: For the atopic patients the positivity to skin prick test and CAP to wheat was in accordance with the immunoblotting results and a food allergy to wheat could be diagnosed. In these patients a major allergen was a 16-kDa band corresponding to members of the cereal alpha-amylase/trypsin inhibitors protein family, the major allergens involved in baker's asthma. In the non-atopic patients the positive immunoblotting results contrasted with the responses of the allergologic tests, indicating that the allergenic wheat protein preparations currently used are of limited value in detecting specific IgE to wheat and that the fraction of irritable bowel syndrome (IBS) patients with food allergy may be larger than believed.


Subject(s)
Colonic Diseases, Functional/complications , Colonic Diseases, Functional/metabolism , Flour/adverse effects , Hypersensitivity, Immediate/diagnosis , Hypersensitivity, Immediate/metabolism , Immunoglobulin E/metabolism , Triticum/adverse effects , Triticum/metabolism , Wheat Hypersensitivity/diagnosis , Wheat Hypersensitivity/metabolism , Adult , Electrophoresis, Polyacrylamide Gel , False Negative Reactions , Female , Humans , Hypersensitivity, Immediate/complications , Immunoblotting , Male , Middle Aged , Protein Binding , Solubility , Triticum/immunology , Wheat Hypersensitivity/complications
8.
J Agric Food Chem ; 49(11): 5668-73, 2001 Nov.
Article in English | MEDLINE | ID: mdl-11714375

ABSTRACT

The effect of baking and digestion on the allergenicity of wheat flour proteins has been studied. Pooled sera of patients suffering from food allergy to wheat products were tested for IgE binding to the proteins of the wheat dough and of the bread crumb and crust, before and after being in vitro digested. During in vitro digestion, the IgE binding protein components of the unheated dough tended to disappear, whereas a permanence of IgE recognition was evident for both the bread crumb and crust. This indicates that the baking process increases the resistance of the potential allergens of the wheat flour to proteolytic digestion, allowing them to reach the gastrointestinal tract, where they can elicit the immunological response. Therefore, the effects of baking must be carefully considered in studying food allergies to wheat products.


Subject(s)
Bread , Cooking , Digestion , Wheat Hypersensitivity , Electrophoresis, Polyacrylamide Gel , Humans , Immunoglobulin E/blood , In Vitro Techniques , Plant Proteins/metabolism , Protein Binding
9.
J Gastroenterol ; 34(3): 345-50, 1999 Jun.
Article in English | MEDLINE | ID: mdl-10433010

ABSTRACT

The correlation between therapeutic response and liver fibrogenesis was studied in serum and liver specimens taken from 31 patients treated with alpha-interferon (IFN) (14 sustained responders and 17 non-responders) for chronic hepatitis C. Serum samples, collected before therapy, and at further 6-month intervals over 2 years, were tested for markers of liver neofibrogenesis. Serum N-terminal procollagen III peptide (PIIINP) displayed a significant and persistent decrease (P < 0.05) in sustained responders but not in non-responders; significantly lowered (P < 0.05) mean levels of C-terminal procollagen I peptide (PICP) were transiently observed in both patient groups, apparently as a result of IFN administration. Serum laminin (Lam) levels remained unchanged. One year after the cessation of treatment, liver biopsy re-testing showed an improvement in necro-inflammatory scores only in sustained responders, with the histological fibrosis scores remaining unaltered in both groups. IFN treatment seemed to exert an influence on serum levels of markers of hepatic connective tissue turnover even in patients that did not respond to therapy, while no effect was observed on preexistent liver fibrosis.


Subject(s)
Antiviral Agents/therapeutic use , Hepatitis C, Chronic/blood , Hepatitis C, Chronic/drug therapy , Interferon-alpha/therapeutic use , Liver Cirrhosis/pathology , Peptide Fragments/blood , Procollagen/blood , Adult , Analysis of Variance , Biomarkers/blood , Biopsy, Needle , Female , Hepatitis C, Chronic/pathology , Humans , Linear Models , Male , Middle Aged , Prognosis , Retrospective Studies , Sensitivity and Specificity , Treatment Outcome
10.
Am J Gastroenterol ; 94(7): 1892-7, 1999 Jul.
Article in English | MEDLINE | ID: mdl-10406255

ABSTRACT

OBJECTIVE: Irritable bowel syndrome (IBS) is a common gastrointestinal disorder with clinical signs typical of "intestinal" food allergies or intolerance. The aim of this study was to characterize the clinical features of IBS patients suspected of suffering from adverse reactions to food. METHODS: The study involved 128 consecutive IBS patients divided into four groups according to their main symptom on presentation at our outpatient clinic. A detailed medical history was recorded, paying particular attention to any allergies and reported intolerance to food. Each patient was screened for allergies; intestinal permeability tests was performed in randomly selected patients from different groups. Findings were analyzed using the chi2 test. RESULTS: Adverse reactions to one or more foods were reported by 80 patients (62.5%); skin prick tests (SPT) were positive in 67 patients (52.3%) with no significant differences between patients complaining of different symptoms. Patients who reported a food intolerance had more positive SPTs than those who did not (47 of 80 [58.7%] vs 20 of 48 [41.7%]); this difference was not statistically significant, although it suggests a trend (p < 0.0610). There was little consistency between the specific foods reported to cause intolerance and those resulting from the tests (11 of 80 patients, 13.7%). The intestinal permeability test was normal in 29 of 33 patients (87.9%). CONCLUSIONS: More than 50% of IBS patients were found sensitized to some food or inhalant without any typical clinical signs. Patients were unable to identify potentially offending foods. The lack of a correlation between SPT results and reported food allergies needs further investigation to clarify the pathophysiology and improve the diagnosis of intestinal food allergies.


Subject(s)
Colonic Diseases, Functional/immunology , Food Hypersensitivity/diagnosis , Adolescent , Adult , Aged , Allergens , Colonic Diseases, Functional/complications , Colonic Diseases, Functional/diagnosis , Female , Food/adverse effects , Food Hypersensitivity/complications , Humans , Intestinal Absorption , Male , Middle Aged , Sensitivity and Specificity , Skin Tests
11.
Ann Ital Med Int ; 13(3): 152-6, 1998.
Article in Italian | MEDLINE | ID: mdl-9859571

ABSTRACT

Recurrent aphthous stomatitis is a frequently occurring disorder which may be a clinical feature of systemic disease. For many other patients, it is a tedious problem often having no known cause. The aim of this study was to verify if immune responses to common foods and/or viruses are involved in the etiopathogenesis of recurrent aphthous stomatitis. Sixteen patients with this disorder were studied by measurement of immunoglobulin classes (IgG, IgA, IgM), blood lymphocyte subpopulations, blood circulating immune complexes, and complement fractions (C3 and C4). Intradermal skin tests for common food and inhalant allergens were performed in all cases. In 5 patients with positive skin tests, serum specific IgE were tested for the same allergens by radioallergosorbent test. Skin patch tests for dental material were performed in all cases. Oral mucosal biopsies and/or cytology samples were taken in 10 cases for histopathological evaluation and in situ hybridization for Papillomavirus, Cytomegalovirus, Herpes simplex virus I and II, Epstein Barr virus. In 13 patients, lymphocyte subpopulations were altered, with a reduced CD4/CD8 ratio. No other alterations of serum immunological parameters were observed. Skin patch tests for dental material were negative in all cases, while skin tests for food allergens were positive in 5 cases (not confirmed by radioallergosorbent test or food challenge tests). Virus antigen and DNA were not found in mucosal specimens, although one patient was positive for Epstein Barr virus DNA by in situ hybridization. An alteration of the CD4/CD8 ratio was demonstrated in most of the patients with recurrent aphthous stomatitis, although immune responses to food and/or dental material and/or common viruses did not seem to be involved in the etiopathogenesis of this disorder.


Subject(s)
Antibodies, Viral/analysis , Dental Materials/adverse effects , Food Hypersensitivity/complications , Immunoglobulins/analysis , Stomatitis, Aphthous/immunology , Adult , Complement System Proteins/analysis , Female , Humans , Male , Recurrence , Skin Tests , Stomatitis, Aphthous/etiology
12.
Minerva Pediatr ; 50(5): 157-61, 1998 May.
Article in Italian | MEDLINE | ID: mdl-9842212

ABSTRACT

BACKGROUND: Cord blood IgE levels have been studied as a possible marker of allergy in infants but few studies are available in our Region. The aim of this paper was to test IgE levels in cord blood of 60 consecutive newborns in a restricted area of Veneto, to correlate cord blood IgE levels with family history of allergy and to verify the risk of contamination from mother's blood. METHODS: Cord blood was obtained from 60 consecutive newborns. Immunoglobulin levels (IgG, IgA, IgM, and IgE) were measured in cord blood of newborns and in serum of all mothers. Family history for allergy was previously investigated from the mothers. RESULTS: IgE were detectable in cord blood of 5 newborns but only 2 of them had positive family history for allergy which was pointed out in 11/60. In one of these cases the contamination of sample from mother's blood was postulated. IgG levels in newborn cord blood were higher than in mothers' blood and it was not related with IgE levels or other investigated factors. CONCLUSIONS: Only 6.6% of newborns in a restricted area of Veneto region have detectable IgE in cord blood whereas 18.3% of them have positive family history for allergy. Measurable levels of IgE in cord blood are not related with positive family history of allergy and are rarely influenced by mothers' blood contamination.


Subject(s)
Fetal Blood/immunology , Hypersensitivity/immunology , Immunoglobulin E/blood , Adult , Female , Humans , Immunoglobulin A/blood , Immunoglobulin A/immunology , Immunoglobulin G/blood , Immunoglobulin G/immunology , Immunoglobulin M/blood , Immunoglobulin M/immunology , Infant, Newborn , Italy
13.
Ital J Gastroenterol Hepatol ; 30(1): 71-6, 1998 Feb.
Article in English | MEDLINE | ID: mdl-9615270

ABSTRACT

AIMS: Interferon alpha has been reported to enhance autoantibody production and to increase the risk of autoimmunity particularly against thyroid tissue. We designed a study with the following aims: 1) to assess the incidence of organ- and non-organ-specific autoantibodies during Interferon treatment; 2) to evaluate whether these autoantibodies have any clinical relevance; 3) to establish whether the development of autoimmune disorders can be related to a genetic predisposition. METHODS: A panel of 5 non-organ-specific and 6 organ-specific autoantibodies was evaluated in serum samples collected before treatment and then at 3 and 12 months in 47 patients enrolled in a treatment protocol with a 2b-recombinant Interferon (3 MU, 3 times a week for 12 months). In the second part of the study we explored genetic predisposition for autoimmune disorders in 31 patients by DNA-HLA class II typing using Restriction Fragment Length Polymorphism (RFPL). RESULTS: Non-organ-specific autoantibodies were absent in all patients before and after Interferon. During follow-up 6 patients showed an increment in thyroid microsomal antibody titres; 3 of these also developed thyroglobulin autoantibodies; 3 of the 6 patients developed persistent hypothyroidism; a fourth had a transient subclinical hypothyroidism and a fifth had a transient subclinical hyperthyroidism. Two patients with initial positivity for ICA and PCA maintained their reactivity during treatment without impairment of the respective target organs. Eight out of 39 initially negative patients developed one or more organ-specific autoantibodies during follow-up. One of these developed a persistent hypothyroidism, and another developed insulin-dependent diabetes. HLA-typing did not reveal any particular allele frequency in patients with thyroid antibody positivity as compared with those without autoantibodies and controls. Moreover, four of the 6 patients positive for islet-cell antibodies were carrying the non-Asp 57 allele which is considered a marker of a genetic predisposition for insulin-dependent diabetes. CONCLUSIONS: These findings suggest that, besides the thyroid gland, pancreatic beta-cells could be a target of autoimmunity during Interferon-treatment for chronic HCV hepatitis. A genetic predisposition may be important, though insufficient alone, in the development of Interferon-induced autoimmune phenomena.


Subject(s)
Antiviral Agents/therapeutic use , Autoantibodies/analysis , Autoimmune Diseases/genetics , Hepatitis C, Chronic/therapy , Histocompatibility Antigens Class II/genetics , Interferon-alpha/therapeutic use , Adolescent , Adult , Autoimmune Diseases/immunology , Autoimmunity , Child , Child, Preschool , DNA/analysis , Electrophoresis, Polyacrylamide Gel , Female , Follow-Up Studies , Hepatitis C/immunology , Hepatitis C Antibodies/analysis , Hepatitis C, Chronic/immunology , Histocompatibility Antigens Class II/immunology , Humans , Interferon alpha-2 , Islets of Langerhans/immunology , Male , Middle Aged , Polymerase Chain Reaction , Polymorphism, Restriction Fragment Length , Prospective Studies , Recombinant Proteins , Thyroglobulin/immunology , Thyroid Gland/immunology
14.
Ital J Gastroenterol ; 28(3): 160-2, 1996 Apr.
Article in English | MEDLINE | ID: mdl-8789827

ABSTRACT

Gastric ectopias in the upper oesophagus and hypopharynx are relatively rare and often misinterpreted. They may become symptomatic due to the onset of a fistula involving adjacent structures in the neck. This case report describes a 20-year-old patient with swallowing difficulties and laterocervical pain, with a diagnosis of fistula of the pyriform sinus due to secernent gastric mucosal ectopia. The significance of this case lies in the fact that accurate aetiopathogenic study and careful differential diagnostic procedures enabled the proper identification of this rare upper oesophageal pathology, which is often misdiagnosed due to the technical difficulties involved in conventional endoscopy of the digestive tract.


Subject(s)
Barrett Esophagus/complications , Fistula/etiology , Pharyngeal Diseases/etiology , Adult , Barrett Esophagus/diagnosis , Fistula/diagnosis , Fistula/surgery , Humans , Male , Pharyngeal Diseases/diagnosis , Pharyngeal Diseases/surgery
15.
J Clin Lab Anal ; 9(4): 230-3, 1995.
Article in English | MEDLINE | ID: mdl-7562239

ABSTRACT

A low-molecular-weight form of human chorionic gonadotropin (hCG), urinary gonadotropin peptide (UGP), has been isolated from the urine of pregnant women and of patients with cancer, mainly of gynecological origin. The clinical value of UGP measurement in gynecological diseases is under investigation but a preliminary study is necessary in order to ascertain whether there is a circadian rhythm in UGP production, to clarify the best way to express the results, and to establish the cutoff and decisional values. In our work we demonstrated a significant correlation between the UGP output and the UGP excretion normalized for urinary creatinine. A very significant agreement was even found in 24-hr urine collections and UGP concentration of a single morning specimen from the same patients. No evident circadian rhythm was found, although some patients presented morning levels of UGP higher than in other collections. UGP postmenopausal levels were higher than premenopausal. The cutoff level, adopting the 95.0 percentile, was 200 pmol/mol creatinine.


Subject(s)
Biomarkers, Tumor/urine , Chorionic Gonadotropin, beta Subunit, Human/urine , Genital Diseases, Female/urine , Peptide Fragments/urine , Adolescent , Adult , Aged , Circadian Rhythm , Creatinine/urine , Female , Humans , Middle Aged , Postmenopause , Pregnancy , Premenopause , Sensitivity and Specificity , Specimen Handling
16.
Minerva Gastroenterol Dietol ; 40(1): 1-9, 1994 Mar.
Article in Italian | MEDLINE | ID: mdl-8204699

ABSTRACT

Allergic mechanisms have been shown to induce gastric and intestinal damage in animal models. It has been demonstrated that people allergic to food may complain of gastrointestinal disorders. Furthermore food allergens can induce gastric mucosal damage in sensitized people. Little is known as regards allergic mechanisms underlying "peptic" ulcers although there are reports suggesting that some forms of gastric and duodenal ulcer may be caused by allergy. AIM. Of the study was to evidence if IgE specific to food and inhalants are localized in gastric and duodenal mucosa and if the in vitro incubation of gastric and duodenal biopsies with specific allergens, stimulate mast-cell mediators. MATERIALS AND METHODS. Twenty-one patients affected by gastric/duodenal ulcers (14 with high total IgE serum levels) and 16 controls were studied. All patients were submitted to upper digestive endoscopy and biopsies were taken from gastric fundus, body and antrum and duodenal bulb. Specific IgE to food and inhalant allergens were tested after homogenization of biopsies, using commercial kits. In 3 selected patients, 3 biopsies from gastric fundus and 3 from duodenal bulb were taken. After incubation of mucosal of mucosal biopsies with allergens (wheat, lactoalbumin, Parietaria J. pollen), the release of histamine and tryptase was measured. The release of Pepsinogen A was measured in the same conditions, as control. RESULTS. Specific IgE to food and inhalants allergens have been found in 164/586 tests (27.9%) of "peptic" ulcer patients and in 17/430 tests (4%) of controls. The duodenal bulb resulted the site in which most frequently IgE have been found. The release of histamine and tryptase has been stimulated only in 1/6 tests by incubation of biopsies with specific allergens in patients with specific IgE. PG-A release has been always stimulated by incubation of gastric biopsies, but not duodenal biopsies, with all tested allergens. DISCUSSION AND CONCLUSION. Specific IgE may be localized in gastric and duodenal mucosa of patients with "peptic" ulcer and/or food allergy. This event is linked to high total IgE serum levels and in a lesser extent, intestinal parasitosis, it is not strictly correlated with specific IgE in the serum and it regards both food and inhalant allergens. No relevant effects were observed after incubation of specific allergens with gastric or duodenal mucosa biopsies containing specific IgE. The possibility that higher allergens concentration stimulate mediator release from mast cells should be investigated. A defect of the gastric or duodenal epithelial barrier which permit a passage way for proteins with subsequent IgE production in the submucosa, appears to be the cause of localization of specific IgE in stomach and duodenum.


Subject(s)
Antibody Specificity , Duodenal Ulcer/immunology , Duodenum/immunology , Gastric Mucosa/immunology , Immunoglobulin E/analysis , Intestinal Mucosa/immunology , Stomach Ulcer/immunology , Adult , Aged , Biopsy , Duodenal Ulcer/etiology , Duodenal Ulcer/pathology , Duodenum/pathology , Endoscopy, Digestive System , Female , Gastric Mucosa/pathology , Humans , Intestinal Mucosa/pathology , Male , Middle Aged , Stomach Ulcer/etiology , Stomach Ulcer/pathology
17.
Ital J Gastroenterol ; 26(1): 7-11, 1994.
Article in English | MEDLINE | ID: mdl-7912969

ABSTRACT

The prevalence of high total IgE serum levels was evaluated in 232 consecutive patients suffering from peptic ulcer. Twenty-one percent of the patients presented total IgE serum levels above 200 KU/L compared with the 5% found in a healthy control population (p < 0.004). Similar prevalence was found in gastric and/or duodenal ulcers. No significant differences in the duration of the disease, smoking habits, familiarity for peptic ulcer, symptomatology and frequency of complications were observed between patients with high and with normal total IgE serum levels. Gastric function studies (gastric acid secretion, serum pepsinogen and gastrin levels) did not show any significant differences between the two groups. The incidence of Helicobacter pylori infection was 65% in patients with normal IgE levels and 75% in those with high IgE levels (p: n.s.). The response to treatment with full dose of H2-receptor antagonists was comparable in both groups (91.25% and 90.7% of ulcer healing after 6-8 weeks of treatment). A relapse of the ulcer after 6 months of maintenance therapy (half dose of H2-receptor antagonists) was observed in 39.5% of the patients with ulcer and high total IgE serum as against the 11.9% observed in patients with normal IgE (p < 0.001). These data lend further support to the hypothesis of an underlying immuno-allergic reaction in some forms of gastric or duodenal ulcer.


Subject(s)
Immunoglobulin E/blood , Peptic Ulcer/blood , Adolescent , Adult , Aged , Aged, 80 and over , Duodenal Ulcer/blood , Duodenal Ulcer/complications , Duodenal Ulcer/drug therapy , Duodenal Ulcer/immunology , Duodenal Ulcer/microbiology , Female , Follow-Up Studies , Food Hypersensitivity/complications , Gastric Acid/metabolism , Gastrins/blood , Helicobacter Infections/complications , Helicobacter Infections/epidemiology , Helicobacter Infections/microbiology , Helicobacter pylori , Histamine H2 Antagonists/therapeutic use , Humans , Male , Middle Aged , Peptic Ulcer/complications , Peptic Ulcer/drug therapy , Peptic Ulcer/immunology , Peptic Ulcer/microbiology , Prevalence , Prostaglandins A/blood , Recurrence , Stomach Ulcer/blood , Stomach Ulcer/complications , Stomach Ulcer/drug therapy , Stomach Ulcer/immunology , Stomach Ulcer/microbiology , Treatment Outcome
20.
Ital J Gastroenterol ; 23(2): 81-5, 1991 Feb.
Article in English | MEDLINE | ID: mdl-1747509

ABSTRACT

Eosinophilic Gastroenteritis (EG) is a poorly understood disorder defined by eosinophilic infiltration of the bowel wall, eosinophilia and gastrointestinal symptoms. The disease's aetiology, course and treatment are not well known. We report two atypical cases of EG: one involving the mucosal layer and another involving the serosal and muscularis layer. The first shows how EG may present with a long history of episodes of intestinal obstruction and malabsorption and how the disease could take a severe course and may be unresponsive to treatment. The second case shows EG presenting as acute abdomen and which subsequently became asymptomatic without therapy, regardless of the fact that peripheral eosinophilia remained present. This case raises the problem of how to treat an asymptomatic patient, what parameters should be considered in order to assess the progress of the disease and the indications for treatment.


Subject(s)
Eosinophilia/pathology , Gastroenteritis/pathology , Adult , Eosinophilia/drug therapy , Female , Gastroenteritis/drug therapy , Humans , Intestinal Absorption , Intestinal Mucosa/pathology , Middle Aged , Prednisone/therapeutic use , Prognosis , Treatment Outcome
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