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Featured researches published by Lorello D.


The Journal of Allergy and Clinical Immunology | 1996

Gastroesophageal reflux and cow's milk allergy in infants : A prospective study

Giuseppe lacono; Antonio Carroccio; F. Cavataio; Giuseppe Montalto; Kazmierska I; Lorello D; Maurizio Soresi; Alberto Notarbartolo

BACKGROUND Recent reports have suggested that gastroesophageal reflux in pediatric patients may be caused by food allergy. OBJECTIVE The aim of our study was to determine the frequency of the association of gastroesophageal reflux with cows milk protein allergy in patients win the first year of life. METHODS We studied 204 consecutive patients (median age, 6.3 months) who had been diagnosed as having gastroesophageal reflux on the basis of 24-hour continuous pH monitoring and histologic examination of the esophageal mucosa. RESULTS Clinical history suggested diagnosis of cows milk allergy in 19 infants, and 93 others had positive test results (serum IgE anti-lactoglobulin, prick tests, circulating or fecal or nasal mucus eosinophils) but did not have symptoms indicating cows milk allergy. The cows milk-free diet and two successive blind challenges confirmed the diagnosis of cows milk allergy in 85 of the 204 patients with gastroesophageal reflux. The clinical presentations of the infants with gastroesophageal reflux alone were different, in view of the greater frequency of diarrhea (p less than 0.0001) and atopic dermatitis (p less than 0.0002). In all, gastroesophageal reflux was associated with, and probably caused by cows milk allergy, in 85 of 204 cases (41.8%). CONCLUSIONS Considering the frequency of this association, patients younger than 12 months old with symptoms of gastroesophageal reflux should be carefully examined to determine whether this disorder is primary or caused by cows milk allergy.


Scandinavian Journal of Gastroenterology | 1992

Gastric emptying in infants with gastroesophageal reflux. Ultrasound evaluation before and after cisapride administration.

Antonio Carroccio; Giuseppe Iacono; G. Li Voti; Giuseppe Montalto; F. Cavataio; V. Tulone; Lorello D; Kazmierska I; C. Acierno; Alberto Notarbartolo

The present study aimed to evaluate gastric emptying in children with gastroesophageal reflux (GER) by means of real-time ultrasonography, on the basis of measurements of the cross-sectional area of the gastric antrum. Twelve children with GER were studied (seven males, five females; age range, 3-13 months) and compared with 12 normal control children (six males, six females; age range, 3-13 months). The diagnosis of GER was confirmed by 24-h esophageal pH-monitoring. The GER patients had a significantly greater antral area than the controls at 90, 105, and 120 min after eating a standard meal (cows milk formula, 300 ml/m2 body surface area); in addition, final gastric emptying time was significantly greater in the patients than in the controls (145 +/- 36.9 versus 78.7 +/- 19.3 min; p less than 0.0025). After 8 weeks of treatment with cisapride (0.3 ml/kg, three times a day) 24-h esophageal pH-monitoring and ultrasonography studies were repeated in the patients. The total percentage reflux time was significantly lower (p less than 0.038), and ultrasonography showed a decreased antral area at all the various study times, with no significant difference between patients and controls; final gastric emptying time was also significantly lower than before treatment (p less than 0.009). Furthermore, in the GER patients there was a significant correlation between gastric emptying time and the sum of the various reflux times recorded in the 2 h after all meals over the 24 h.(ABSTRACT TRUNCATED AT 250 WORDS)


Digestive Diseases and Sciences | 1995

Pancreatic enzyme therapy in childhood celiac disease : a double-blind prospective randomized study

Antonio Carroccio; Giuseppe Iacono; Giuseppe Montalto; F. Cavataio; Lorello D; L. Greco; Maurizio Soresi; Alberto Notarbartolo

The validity of pancreatic enzyme substitution therapy in the two months following diagnosis of celiac disease was investigated. Twenty patients (8 males, 12 females), mean age 14.2 months (group A) received an enzyme substitution preparation. The control group (group B) included 20 patients (9 males, 11 females), mean age 14.5 months, treated with placebo. Before starting treatment, we performed a stratification for age, weight-for-age at diagnosis, and degree of pancreatic insufficiency. The therapies were then administered randomly in double-blind fashion. On diagnosis and 30 and 60 days after commencement of a gluten-free diet with identical calorie intake in both groups, a series of anthropometric variables were determined. After 30 days weight increase in group A patients was significantly higher (in grams) than in group B: 1131±461 vs 732±399 (P<0.006). Weight-for-age increase also was greater in group A than in group B: 9.2±5.1% vs 5.0±4.0% (P<0.002). The increase in height Z score, weight-for-height, arm circumference, and subscapular and tricipital fold measurements were greater in group A patients than those in group B, but the difference was not significant. After 60 days of therapy none of the parameters considered were significantly different in the two groups. We concluded that pancreatic enzyme therapy is certainly useful in the first 30 days after diagnosis of celiac disease.


Digestive Diseases and Sciences | 1994

Pancreatic insufficiency in celiac disease is not dependent on nutritional status

Antonio Carroccio; Giuseppe Iacono; Giuseppe Montalto; F. Cavataio; Lorello D; Maurizio Soresi; D. Di Martino; Alberto Notarbartolo

To determine the relationship between pancreatic secretory capacity and nutritional status in celiac patients, we studied 52 patients with celiac disease (24 males, 28 females; age range 6–36 months) and 30 healthy control subjects (14 males, 16 females; age range 6–42 months). A secretin-cerulein test was performed on all patients, and levels of serum albumin and plasma fibronectin were assayed. In addition, weight/height ratios were calculated in the celiacs, who were then divided into three groups on this basis, as follows: celiacs with weight/height ratio≤3rd percentile; those with weight/height ratio between the 4th and 10th percentiles; and those with weight/height ratio>10th percentile. There was no significant difference in the duodenal output of chymotrypsin, phospholipase and lipase between these groups. When the total celiac group was compared to control subjects, only lipase levels were significantly lower (P<0.009). However, subnormal values in one or more pancreatic enzymes were observed in 15/52 celiacs (29%). A residual enzyme activity<10% of normal secretory capacity, was also found in 4/52 patients. There was no correlation between the output of the various pancreatic enzymes and levels of albumin, fibronectin, and weight/height ratios in the patients. Furthermore, there was no difference in weight/height ratio and levels of albumin and fibronectin between the celiac subjects with pancreatic deficiency and those with normal pancreatic function. We conclude that a mild/moderate pancreatic insufficiency is quite frequent in celiacs, but that it may be completely independent of nutritional status; further studies are therefore required to shed light on its pathogenesis.


International Journal of Pancreatology | 1993

Secretin-cerulein test and fecal chymotrypsin concentration in children with intestinal giardiasis

Antonio Carroccio; Giuseppe Iacono; Giuseppe Montalto; F. Cavataio; Lorello D; Alberto Notarbartolo

SummaryWe studied six patients with giardiasis (five males, one female), median age 3.5 yr (range 1–11) and 12 healthy control subjects (10 males, 2 females) median age 3.5 yr (range 1–10). Intestinal biopsy and a contemporaneous secretin-cerulein test were performed in all patients, and fecal chymotrypsin was also assayed. Intestinal biopsy was normal in five of the six patients with giardiasis, whereas one of the six presented a partial atrophy of the intestinal villi. The secretin-cerulein test (1 CU/kg of secretin + 75 ng/kg of cerulein) did not show any significant difference between values in the outputs of chymotrypsin, lipase, phospholipase, and bicarbonate obtained in patients and in controls; however, in the one patient with partial intestinal mucosal atrophy, all enzymatic activity levels were below the normal limit for our laboratory. Furthermore, the mean values of fecal chymotrypsin concentration did not differ between the two groups. Fecal chymotrypsin was also reduced in the patient with an abnormal secretin-cerulein test; a second assay performed 3 mo after the suspension of treatment (Metronidazole), however, showed a normal chymotrypsin concentration.


International Journal of Pancreatology | 1992

Pancreatic enzymes in chronic renal failure and transplant patients

Giuseppe Montalto; Antonio Carroccio; Vito Sparacino; Lorello D; Daniela Di Martino; Maurizio Soresi; Antonio Galione; Alberto Notarbartolo

SummaryThe aim of the present study was to determine the frequency and degree of elevated serum levels of Total Amylase (TA), Pancreatic Amylase (PA), and Lipase (L) activity in patients with chronic renal failure (CRF) on conservative therapy; CRP on periodical hemodialysis (HD); in renal transplant (RT) and in a control Group (C). Mean values were significantly higher in all groups than Group C for TA (p < 0.005), PA (p < 0.0001) and L (p < 0.0001). A statistically significant correlation was found between TA and L vs creatininemia values in CRF patients, but only up to a certain level (creatininemia <6 mg%) (p < 0.03 andp < 0.05), above which there was no correlation. The enzyme most frequently over the maximum normal limit was PA, both in the total CRF group (51%), in the hemodialysis patients (65%), and in the RT patients (55%); but only a few patients had values two times higher than the normal limits: 15% in the total CRF, 14% is the hemodialysis, and 10% in the RT groups, respectively. These results suggest that the increase in serum pancreatic enzyme during chronic renal pathology is slight but frequently occurs. It is possible that in these patients together with the renal excretion impairment there could also be some subclinical pancreatic damage; its genesis could also depend on the pharmacological treatment used (diuretics, immunosuppressive drugs) commonly adopted in these pathologies.


Scandinavian Journal of Gastroenterology | 1997

Evaluation of Pancreatic Function Development after Hydrolyzed Protein- Based and Soy-Based Formulas in Unweaned Infants

Antonio Carroccio; F. Cavataio; Giuseppe Montalto; Maurizio Soresi; Lorello D; Alberto Notarbartolo; G. Iacono

AIMS Different protein sources could determine differences in the maturation of the exocrine pancreas in humans during the first months after birth; however, no studies have been carried out in man to evaluate the effect of a hydrolyzed protein diet on exopancreatic function. Our aim was therefore to determine the effect of two different milk formulas on pancreatic secretion in patients with cows milk protein allergy (CMPA). METHODS We selected 12 infants (median age, 3.0 months), fed for 6 weeks with a hydrolyzed casein-based formula, and 14 infants (median age, 3.0 months) who received a soy-protein based formula over the same period. As controls, two groups of age-matched infants with no gastrointestinal disease and receiving a free diet were studied. In the patients with CMPA a secretin-cerulein test was performed at the commencement of the diet and after 6 weeks; in the controls the same test was performed only once. Enzyme concentrations and outputs of trypsin, chymotrypsin, lipase, and phospholipase were assayed. RESULTS No significant difference was observed between the two groups of patients with CMPA for any of the enzymes studied, either at base line or after 6 weeks of diet. No difference was recorded between CMPA patients and age-matched controls on a free diet either. In both CMPA groups there was a significant increase over basal values in trypsin, chymotrypsin, and lipase concentrations after 6 weeks. Furthermore, there was a significant positive correlation between the age of the patients and enzyme concentrations. Mean daily weight gain was 27.4 +/- 3.9 g with hydrolyzed casein and 27.2 +/- 3.5 g in soyfed patients. CONCLUSIONS It is suggested that the diets with different protein content used in subjects with CMPA did not determine any difference in the stimulation of proteolytic and lipolytic pancreatic enzymes.


Journal of Nutritional & Environmental Medicine | 1997

Diet and gallstones in women of a rural town of Sicily

Giuseppe Montalto; Antonio Carroccio; Maurizio Soresi; Cartabellotta A; Lorello D; Giovanni Cavera; Maurizio Averna; Carlo M. Barbagallo; G. Anastasi; Bascone F; Alberto Notarbartolo

To test the possible association between dietary factors and gallstones, we performed a case-control study on the dietary habits of 71 women with gallstones in a rural area of Sicily (mean age 63.2 years) and compared these with 142 women who did not have gallstones (mean age 63.6 years) selected at random from the same general population. The dietary questionnaire, based on data collected over 7 days, was carefully compiled by two dieticians specially trained for the study. The daily calorie intake was higher in the women with gallstones ( p= 0.006) and was equally distributed between fats, carbohydrates and proteins. The intakes of unsaturated fats ( p= 0.03), unrefined sugars ( p= 0.01) and fibre ( p= 0.04) were significantly higher in the subjects with gallstones. The cholesterol and calcium intakes were not significantly different, although the average consumption in both groups was lower than the recommended quantities. However, all the nutrients were equally distributed in percentage between the tw...


Journal of Pediatric Gastroenterology and Nutrition | 1991

Severe infantile colic and food intolerance: a long-term prospective study.

Giuseppe Iacono; Antomio Carroccio; Giuseppe Montalto; F. Cavataio; Elisabetta Bragion; Lorello D; V. Balsamo; Alberto Notarbartolo


The Italian journal of gastroenterology | 1995

IgG anti-betalactoglobulin (betalactotest) : its usefulness in the diagnosis of cow's milk allergy

G. Iacono; Antonio Carroccio; F. Cavataio; Giuseppe Montalto; Lorello D; Kazmierska I; Maurizio Soresi

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G. Iacono

Boston Children's Hospital

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