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Tytuł:
Small intestine bacterial overgrowth is frequent in cystic fibrosis: combined hydrogen and methane measurements are required for its detection
Autorzy:
Lisowska, Aleksandra
Wójtowicz, Jerzy
Walkowiak, Jarosław
Powiązania:
https://bibliotekanauki.pl/articles/1040476.pdf
Data publikacji:
2009
Wydawca:
Polskie Towarzystwo Biochemiczne
Tematy:
cystic fibrosis
small intestine bacterial overgrowth
breath test
hydrogen
methane
Opis:
Introduction: Hydrogen breath test (BT) is commonly used as a diagnostic tool for the detection of small intestine bacterial overgrowth (SIBO). It was reported that colonic methane production is far more frequent in cystic fibrosis (CF) patients than in other subjects. Therefore, measuring exclusively hydrogen in the diagnostic breath test for diagnosing SIBO might be of limited value. We aimed to assess the usefulness of combined measurement of hydrogen and methane expiration for the diagnosis of SIBO in CF. Material and Methods: The study comprised 62 CF patients aged 5 to 18 years. Three-hundred-ninety subjects assessed due to gastrointestinal symptoms for the presence of SIBO served as a comparative group. In all subjects hydrogen/methane BT using glucose was performed. A positive BT was defined as fasting hydrogen ≥ 20 ppm or fasting methane ≥ 10 ppm or a rise of ≥ 12 ppm hydrogen or ≥ 6 ppm methane over baseline during the test. Results: In 23 (37.1%) CF patients and in 52 (13.3%) subjects from the comparative group abnormal BT results were found. In seven (11.3%) CF patients and 29 (7.4%) of the other subjects studied methane measurement allowed diagnosis of SIBO. Conclusions: Small intestine bacterial overgrowth is frequent in cystic fibrosis. For its detection in cystic fibrosis and other gastrointestinal patients, combined hydrogen and methane measurement instead of hydrogen breath test should be applied. Without the additional measurement of methane a significant percentage of SIBO will be missed.
Źródło:
Acta Biochimica Polonica; 2009, 56, 4; 631-634
0001-527X
Pojawia się w:
Acta Biochimica Polonica
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Adult-type hypolactasia and lactose malabsorption in Poland
Autorzy:
Mądry, Edyta
Lisowska, Aleksandra
Kwiecień, Jarosław
Marciniak, Ryszard
Korzon-Burakowska, Anna
Drzymała-Czyż, Sławomira
Mojs, Ewa
Walkowiak, Jarosław
Powiązania:
https://bibliotekanauki.pl/articles/1042735.pdf
Data publikacji:
2010
Wydawca:
Polskie Towarzystwo Biochemiczne
Tematy:
lactose malabsorption
hypolactasia
genetic predisposition
lactose intolerance
Opis:
Background: The available data on the incidence of lactose malabsorption are contradictory. Potential bias in random selection is a major drawback of studies performed to-date. Moreover, molecular analysis of polymorphism -13910 C>T upstream of the lactase (LCT) gene (NM_005915.4:c.1917+326C>T; rs4988235) has not been reported in those studies. Therefore, in this study we aimed to assess genetic predisposition and clinical manifestation of adult-type hypolactasia (ATH). Patients and methods: In two-hundred randomly chosen healthy subjects (HS) aged from 18 to 20 years, the presence of -13910 C>T polymorphic variants upstream of the LCT gene was assessed. In a subgroup of subjects with genotype predisposing to ATH, hydrogen-methane breath test (BT) with lactose loading was conducted to determine the current state of lactase activity. In addition, clinical symptoms typical for lactose malabsorption were assessed using the questionnaire method. Results: Sixty-three out of 200 (31.5 %) HS had -13910 C/C genotype. Thus, genetically determined lactase persistence is expected in the remaining 137 (68.5 %) subjects. Thirteen out of 53 (24.5 %) HS having -13910 C/C genotype were proved to be lactose intolerant. Recalculating the data for the entire studied population it implies the incidence of lactose malabsorption in 7.7 % of subjects. Only three out of 13 (23.1 %) subjects with abnormal BT results, reported clinical symptoms related to lactose consumption. Conclusions: Significantly lower than previously reported incidence of clinically detectable lactose malabsorption in young healthy adults in Poland has been documented. The -13910 C/C genotype upstream of the LCT gene indicates a predisposition to ATH, but definitely does not define the current ability to tolerate lactose.
Źródło:
Acta Biochimica Polonica; 2010, 57, 4; 585-588
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:
Normal levels of serum pancreatic enzymes in patients with progressive familial intrahepatic cholestasis type 2
Autorzy:
Walkowiak, Jaroslaw
Jankowska, Irena
Lisowska, Aleksandra
Biczysko, Maciej
Wierzbicka, Aldona
Pawłowska, Joanna
Powiązania:
https://bibliotekanauki.pl/articles/1042733.pdf
Data publikacji:
2010
Wydawca:
Polskie Towarzystwo Biochemiczne
Tematy:
pancreatitis
pancreatic enzymes
lipase
progressive familial intrahepatic cholestasis type 2
elastase-1
Opis:
Introduction. High prevalence of elevated serum pancreatic enzymes in children with cholestasis with normal fecal elastase-1 concentrations has been documented. However, this state is related predominantly to biliary atresia. Therefore, we aimed to assess pancreatic damage by measuring serum pancreatic enzymes in patients with progressive familial intrahepatic cholestasis type 2 (PFIC type 2). Materials and methods. Twenty PFIC type 2 patients with normal serum bilirubin and bile acid concentrations were included in the study. Thirty pancreatic insufficient cystic fibrosis (PI-CF) patients, thirty patients with acute pancreatitis (AP) and thirty healthy subjects (HS) served for the purpose of comparison. In all subjects, serum lipase and elastase-1 levels were measured. Results. In all but one PFIC type 2 patients and all HS normal lipase activities were found. Serum elastase-1 concentrations were normal in all PFIC type 2 patients and HS. The enzyme levels were very similar in both groups studied. Lipase activities in PFIC type 2 patients were significantly higher than in PI-CF patients (p < 0.00001) and lower than in patients with AP (p < 0.00001). Serum elastase-1 levels in PFIC type 2 patients were significantly lower than in patients with AP (p < 0.00001) and not different from those in PI-CF patients. In conclusion. serum pancreatic enzymes in patients with PFIC type 2 are normal. No pancreatic damage in these patients could be detected.
Źródło:
Acta Biochimica Polonica; 2010, 57, 4; 573-575
0001-527X
Pojawia się w:
Acta Biochimica Polonica
Dostawca treści:
Biblioteka Nauki
Artykuł
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:
Badania rezonansu magnetycznego u chorych na mukowiscydozę: wielkość trzustki
Autorzy:
Jończyk-Potoczna, Katarzyna
Sosnowski, Piotr
Warzywoda, Małgorzata
Stężowska-Kubiak, Sylwia
Lisowska, Aleksandra
Goździk-Spychalska, Joanna
Pogorzelski, Andrzej
Skorupa, Wojciech
Minarowska, Alina
Antczak, Andrzej
Biczysko, Maciej
Walkowiak, Jarosław
Powiązania:
https://bibliotekanauki.pl/articles/552820.pdf
Data publikacji:
2011
Wydawca:
Stowarzyszenie Przyjaciół Medycyny Rodzinnej i Lekarzy Rodzinnych
Tematy:
mukowiscydoza
trzustka
morfologia trzustki
funkcja trzustki
rezonans magnetyczny
Źródło:
Family Medicine & Primary Care Review; 2011, 2; 157-160
1734-3402
Pojawia się w:
Family Medicine & Primary Care Review
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Genotyp a funkcja zewnątrzwydzielnicza trzustki w mukowiscydozie
Autorzy:
Lisowska, Aleksandra
Biczysko, Maciej
Walkowiak, Jarosław
Powiązania:
https://bibliotekanauki.pl/articles/551981.pdf
Data publikacji:
2011
Wydawca:
Stowarzyszenie Przyjaciół Medycyny Rodzinnej i Lekarzy Rodzinnych
Tematy:
mukowiscydoza
genotyp
mutacje genu CFTR
funkcja zewnątrzwydzielnicza trzustki
Źródło:
Family Medicine & Primary Care Review; 2011, 2; 332-333
1734-3402
Pojawia się w:
Family Medicine & Primary Care Review
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Genotyp a morfologia trzustki u chorych na mukowiscydozę
Autorzy:
Jończyk-POtoczna, Katarzyna
Sosnowski, Piotr
Warzywoda, Małgorzata
Stężowska-Kubiak, Sylwia
Lisowska, Aleksandra
Cofta, Szczepan
Pogorzelski, Andrzej
Skorupa, Wojciech
Minarowska, Alina
Antczak, Andrzej
Biczysko, Maciej
Walkowiak, Jarosław
Powiązania:
https://bibliotekanauki.pl/articles/552705.pdf
Data publikacji:
2011
Wydawca:
Stowarzyszenie Przyjaciół Medycyny Rodzinnej i Lekarzy Rodzinnych
Tematy:
mukowiscydoza
genotyp
morfologia trzustki
rezonans magnetyczny.
Źródło:
Family Medicine & Primary Care Review; 2011, 2; 161-164
1734-3402
Pojawia się w:
Family Medicine & Primary Care Review
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Hipolaktazja, zespół złego wchłaniania laktozy, nietolerancja laktozy
Autorzy:
Mądry, Edyta
Krasińska, Beata
Walkowiak, Jarosław
Powiązania:
https://bibliotekanauki.pl/articles/552928.pdf
Data publikacji:
2011
Wydawca:
Stowarzyszenie Przyjaciół Medycyny Rodzinnej i Lekarzy Rodzinnych
Tematy:
hipolaktazja
zespół złego wchłaniania laktozy
nietolerancja laktozy
Źródło:
Family Medicine & Primary Care Review; 2011, 2; 334-336
1734-3402
Pojawia się w:
Family Medicine & Primary Care Review
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Inulin supplementation in rat model of pouchitis
Autorzy:
Drzymała-Czyż, Sławomira
Banasiewicz, Tomasz
Tubacka, Małgorzata
Majewski, Przemysław
Biczysko, Maciej
Kościński, Tomasz
Drews, Michał
Walkowiak, Jarosław
Powiązania:
https://bibliotekanauki.pl/articles/1039892.pdf
Data publikacji:
2011
Wydawca:
Polskie Towarzystwo Biochemiczne
Tematy:
rats
pouchitis
inulin
restorative proctocolectomy
Opis:
Available data indicates potential effectiveness of prebiotic therapy in alleviating inflammation and prolonging the remission in inflammatory bowel disease. Documented successes of such therapies were the basis for this study. So far, there is no data related to the effectiveness of inulin application in symptomatic or severe pouchitis in humans or in animal model. The aim of the study was to determine the effect of inulin supplementation on the expression of intestinal inflammation and feeding efficiency in rats with induced pouchitis. Twenty-four Wistar rats were operated. After induction of pouchitis animals were randomly divided into control and supplementation groups receiving, respectively, semi-synthetic diet with or without inulin (in a lower (LD) or higher (HD) dose: 2.5 % or 5 % of total dietary content of mass) for a period of 6 weeks. Selected nutritional parameters were assessed throughout the study. Histopathological and immunohistochemical analysis of pouch mucosa specimens was also performed. The energy intake, weight gain, feeding efficiency, quality of stools were comparable in all studied groups. The intensity of inflammation (Moskovitz scale) and adaptive changes (Laumonier scale) did not differ between compared groups. The tissue expression of pro- and anti-inflammatory interleukins (IL-1α, IL-6, IL-10 and IL-12) was not different either. Inulin supplementation does not improve the quality of stools or the expression of intestinal inflammation in rats with induced pouchitis. It has no impact on the intensity of pouch adaptation or on feeding efficiency.
Źródło:
Acta Biochimica Polonica; 2011, 58, 3; 381-384
0001-527X
Pojawia się w:
Acta Biochimica Polonica
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Maślany w nieswoistych zapaleniach jelit
Autorzy:
Drzymała-Czyż, Sławomira
Banasiewicz, Tomasz
Biczysko, Maciej
Walkowiak, Jarosław
Powiązania:
https://bibliotekanauki.pl/articles/551999.pdf
Data publikacji:
2011
Wydawca:
Stowarzyszenie Przyjaciół Medycyny Rodzinnej i Lekarzy Rodzinnych
Tematy:
maślany
kwas masłowy
nieswoiste zapalenia jelit
proktokolektomia odtwórcza
Źródło:
Family Medicine & Primary Care Review; 2011, 2; 305-307
1734-3402
Pojawia się w:
Family Medicine & Primary Care Review
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Niedobór witaminy K u niemowląt chorych na mukowiscydozę
Autorzy:
Krzyżanowska, Patrycja
Lisowska, Aleksandra
Woś, Halina
Trawińska-Bartnicka, Maria
Bober, Lyudmyla
Rohovyk, Nataliya
Rachel, Marta
Walkowiak, Jarosław
Powiązania:
https://bibliotekanauki.pl/articles/552145.pdf
Data publikacji:
2011
Wydawca:
Stowarzyszenie Przyjaciół Medycyny Rodzinnej i Lekarzy Rodzinnych
Tematy:
mukowiscydoza, witamina K
niekarboksylowana protrombina
Źródło:
Family Medicine & Primary Care Review; 2011, 2; 171-173
1734-3402
Pojawia się w:
Family Medicine & Primary Care Review
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Nietolerancja laktozy i jej uwarunkowania
Autorzy:
Fidler-Witoń, Ewa
Mądry, Edyta
Krasińska, Beata
Walkowiak, Jarosław
Powiązania:
https://bibliotekanauki.pl/articles/552232.pdf
Data publikacji:
2011
Wydawca:
Stowarzyszenie Przyjaciół Medycyny Rodzinnej i Lekarzy Rodzinnych
Tematy:
laktaza
nietolerancja laktozy
uwarunkowania genetyczne
Źródło:
Family Medicine & Primary Care Review; 2011, 2; 308-310
1734-3402
Pojawia się w:
Family Medicine & Primary Care Review
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Vitamin K status in peritoneally dialyzed patients with chronic kidney disease
Autorzy:
Stankowiak-Kulpa, Hanna
Krzyżanowska, Patrycja
Kozioł, Lidia
Grzymisławski, Marian
Wanic-Kossowska, Maria
Moczko, Jerzy
Walkowiak, Jarosław
Powiązania:
https://bibliotekanauki.pl/articles/1039864.pdf
Data publikacji:
2011
Wydawca:
Polskie Towarzystwo Biochemiczne
Tematy:
dialysis
vitamin K
kidney disease
Opis:
Abnormal vitamin K status was documented in patients with chronic kidney diseases (CKD), especially those undergoing hemodialysis. The data related to patients undergoing peritoneal dialysis (PD) are contradictory. Therefore, in the present study we aimed to evaluate vitamin K status in patients with CKD who are treated with continuous ambulatory PD. Twenty-eight patients entered into the study. Dialysis vintage ranged from 3 to 89 months. Vitamin K status was assessed in all subjects using undercarboxylated prothrombin measurement (PIVKA-II). In addition, total protein and albumin levels, total cholesterol, LDL cholesterol, triglyceride, calcium, urea and creatinine concentrations were determined. PIVKA-II concentrations were abnormal in 13 (46.4 %) subjects. BMI values, both total and LDL cholesterol concentrations were significantly higher in patients with than those without vitamin K deficiency. Moreover, PIVKA II levels correlated with BMI values (r = 0.441, p < 0.019), LDL cholesterol (r = 0.434, p < 0.021) and creatinine (r = 0.406, p < 0.032) concentrations. However, through the use of logistic regression analysis and multiple regression analysis, no clinical factor was documented to be the independent risk factor of vitamin K deficiency. In conclusion, vitamin K deficiency is a frequent condition in peritoneally dialyzed patients. Assessment of vitamin K status should become a standard procedure in this group of patients.
Źródło:
Acta Biochimica Polonica; 2011, 58, 4; 617-620
0001-527X
Pojawia się w:
Acta Biochimica Polonica
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Trace elements and rat pouchitis
Autorzy:
Drzymała-Czyż, Sławomira
Banasiewicz, Tomasz
Walas, Stanisław
Kościński, Tomasz
Wenska-Chyży, Ewa
Drews, Michał
Walkowiak, Jarosław
Powiązania:
https://bibliotekanauki.pl/articles/1039660.pdf
Data publikacji:
2012
Wydawca:
Polskie Towarzystwo Biochemiczne
Tematy:
pouchitis
selective deficiency
restorative proctocolectomy
trace elements
Opis:
The procedure of restorative proctocolectomy is associated with a complete removal of the colon and slight reduction of ileum length, which together can lead to systemic shortages of trace elements. Inflammatory changes in the pouch mucosa may also have some impact. However, there is no data on trace elements in pouchitis. Therefore, in the present study we aimed to assess the effect of acute pouchitis on the status of selected trace elements in rats. Restorative proctocolectomy with the construction of intestinal J-pouch was performed in twenty-four Wistar rats. Three weeks after the surgery, pouchitis was induced. Eight untreated rats created the control group. Liver concentrations of selected micronutrients (Zn, Cu, Co, Mn, Se) were measured in both groups six weeks later, using inductively coupled plasma mass spectrometry. Liver concentrations of trace elements did not differ between the study and the control groups. However, copper, cobalt and selenium concentrations [μg/g] were statistically lower (p<0.02, p<0.05 and p<0.04, respectively) in rats with severe pouchitis (n=9) as compared with rats with mild pouchitis (n=7) [median (range): Cu - 7.05 (3.02-14.57) vs 10.47 (5.16-14.97); Co - 0.55 (0.37-0.96) vs 0.61 (0.52-0.86); Se - 1.17 (0.69-1.54) vs 1.18 (0.29-1.91)]. In conclusion, it seems that acute pouchitis can lead to a significant deficiency of trace elements.
Źródło:
Acta Biochimica Polonica; 2012, 59, 4; 599-601
0001-527X
Pojawia się w:
Acta Biochimica Polonica
Dostawca treści:
Biblioteka Nauki
Artykuł

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