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Wyświetlanie 1-3 z 3
Tytuł:
Antibiotic therapy and fat digestion and absorption in cystic fibrosis
Autorzy:
Lisowska, Aleksandra
Pogorzelski, Andrzej
Oracz, Grzegorz
Skorupa, Wojciech
Cofta, Szczepan
Szydłowski, Jarosław
Socha, Jerzy
Walkowiak, Jarosław
Powiązania:
https://bibliotekanauki.pl/articles/1039883.pdf
Data publikacji:
2011
Wydawca:
Polskie Towarzystwo Biochemiczne
Tematy:
stable isotope breath test
malabsorption
antibiotic therapy
cystic fibrosis
Opis:
Antibiotic therapy in the cystic fibrosis (CF) mouse model has been shown to result in reduced bacterial load of the intestine and significant body mass gain. The effect was suggested to be linked to the improvement of intestinal digestion and absorption. Therefore, we aimed to assess the influence of routinely applied antibiotic therapy in CF patients on fat assimilation. Twenty-four CF patients aged 6 to 30 years entered the study. Inclusion criteria comprised confirmed exocrine pancreatic insufficiency and bronchopulmonary exacerbation demanding antibiotic therapy. Exclusion criteria comprised: antibiotic therapy six weeks prior to the test, liver cirrhosis, diabetes mellitus, oxygen dependency, the use of systemic corticosteroids. In all enrolled CF subjects, 13C-labelled mixed triglyceride breath test (13C MTG-BT) was performed to assess lipid digestion and absorption, before and after antibiotic therapy. Sixteen subjects were treated intravenously with ceftazidime and amikacin, eight patients orally with ciprofloxacin. Cumulative percentage dose recovery (CPDR) was considered to reflect digestion and absorption of lipids. The values are expressed as means (medians). The values of CPDR before and after antibiotic therapy did not differ in the whole studied group [4.6(3.3) % vs. 5.7(5.3) %, p = 0.100] as well as in the subgroup receiving them intravenously [4.6(3.2) % vs. 5.7(5.3) %, p = 0.327] or in that with oral drug administration [4.6(3.4) % vs. 5.7(5.4) %, p = 0.167]. In conclusion, antibiotic therapy applied routinely in the course of pulmonary exacerbation in CF patients does not seem to result in an improvement of fat digestion and absorption.
Źródło:
Acta Biochimica Polonica; 2011, 58, 3; 345-347
0001-527X
Pojawia się w:
Acta Biochimica Polonica
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Cystic fibrosis is a risk factor for celiac disease
Autorzy:
Walkowiak, Jarosław
Blask-Osipa, Anna
Lisowska, Aleksandra
Oralewska, Beata
Pogorzelski, Andrzej
Cichy, Wojciech
Sapiejka, Ewa
Kowalska, Mirosława
Korzon, Michał
Szaflarska-Popławska, Anna
Powiązania:
https://bibliotekanauki.pl/articles/1040437.pdf
Data publikacji:
2010
Wydawca:
Polskie Towarzystwo Biochemiczne
Tematy:
cystic fibrosis
celiac disease
antiendomysial antibodies
genetic predisposition
Opis:
Background: The coexistence of cystic fibrosis (CF) and celiac disease (CD) has been reported. To our knowledge there is no study directly comparing the incidence of CD in CF patients to that in the general population at the same time. There is no published data on genetic predisposition to CD in CF patients either. Therefore, in the present study we aimed to assess the genetic predisposition to CD and its incidence in CF patients comparing it to data from the general population. Patients and methods: Two hundred eighty-two CF patients were enrolled in the study. In 230 CF patients the genetic predisposition to CD (the presence of HLA-DQ2/ DQ8) was assessed. In all CF patients, serological screening for CD was conducted. In patients with positive antiendomysial antibodies (EMA) gastroduenoscopy was offered. Intestinal histology was classified according to modified Marsh criteria. The results of serological CD screening in 3235 Polish schoolchildren and HLA-DQ typing in 200 healthy subjects (HS) were used for comparison. Results: Positive EMA was found in 2.84% of the studied CF patients. The incidence of proven CD was 2.13%. The incidence of CD as well as positive serological screening were significantly more frequent in the CF group than in the general population. The frequency of CD-related HLA-DQ alleles in CF and HS did not differ. Conclusions: Genetic predisposition to celiac disease in cystic fibrosis patients is similar to that of the general population. However, our results suggest that cystic fibrosis is a risk factor for celiac disease development.
Źródło:
Acta Biochimica Polonica; 2010, 57, 1; 115-118
0001-527X
Pojawia się w:
Acta Biochimica Polonica
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Adrenal Tumors - Diagnostics and the Factual Situation
Autorzy:
Krajewska, Ewa
Toutounchi, Sadegh
Fiszer, Patryk
Cieśla, Witold
Pogorzelski, Ryszard
Bednarczuk, Tomasz
Cieszanowski, Andrzej
Łoń, Izabela
Skórski, Maciej
Powiązania:
https://bibliotekanauki.pl/articles/1396721.pdf
Data publikacji:
2012-04-01
Wydawca:
Index Copernicus International
Tematy:
laparoscopic adrenalectomy
adrenalectomy
adrenal tumor
computer tomography
magnetic resonance
retroperitoneal space tumor
laparoscopic surgery
Opis:
The study presented three cases of patients diagnosed with adrenal tumors subject to surgical intervention during the past 6 months in our Department. The patients presented with radiological diagnostic difficulties, as to the character and location of the primary tumor.The aim of the study was to demonstrate differences between radiological examination results and the factual situation observed during the adrenalectomy. In all the presented cases patients' were subject to laparoscopic intervention. In two cases conversion to open surgery was necessary. The histopathological results of the surgically removed samples were as follows: leiomyoma, myoperycytoma and pheochromocytoma. In selected cases imaging examinations might be of limited value, especially when determining the character and location of the primary lesion of the adrenal gland.
Źródło:
Polish Journal of Surgery; 2012, 84, 4; 208-213
0032-373X
2299-2847
Pojawia się w:
Polish Journal of Surgery
Dostawca treści:
Biblioteka Nauki
Artykuł
    Wyświetlanie 1-3 z 3

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