Kinga Kowalska-Duplaga
Jagiellonian University Medical College
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Featured researches published by Kinga Kowalska-Duplaga.
Inflammatory Bowel Diseases | 2011
Andrzej Radzikowski; Aleksandra Banaszkiewicz; Izabella Łazowska-Przeorek; Urszula Grzybowska-Chlebowczyk; Halina Woś; Tomasz Pytrus; Barbara Iwańczak; Kinga Kowalska-Duplaga; Krzysztof Fyderek; Agnieszka Gawrońska; Katarzyna Karolewska-Bochenek; Maria Kotowska; Piotr Albrecht
Background: There are only a few studies on immune response to routine vaccinations in children with inflammatory bowel disease (IBD), despite a strong need for this kind of study. The aim of the study was to evaluate the immunogenicity of an inactivated hepatitis A vaccine (HAV) in IBD pediatric patients compared with healthy controls. Methods: This was an open, prospective, and controlled study on anti‐HAV‐negative children and adolescents age 2‐18 years with IBD. HAV using 720 enzyme‐linked immunosorbent assay (ELISA) units were administered at 0 months and at 6‐12 months. Seroconversion and geometric mean titers were measured after each vaccine dose. The evidence of local and systemic adverse effects for 3 days after the first and second dose of vaccine was registered. Results: A total of 134 subjects (66 patients and 68 controls) completed the whole study course consisting of two doses of vaccine and six serum samples. There was no significant difference in the rate of seroconversion between IBD patients and controls when measured after the second dose of vaccine (97% versus 100%, P = 0.2407), but the rate was significantly lower in the IBD group when measured after the first dose (39% versus 64%, P = 0.00001). The mean geometric titers were statistically significantly lower in the IBD group than in the control group at all of the measured timepoints. There were no serious adverse events related to HAV during the study. Conclusions: HAV is both immunogenic and safe in pediatric patients with IBD. (Inflamm Bowel Dis 2010;)
Inflammatory Bowel Diseases | 2012
Aleksandra Banaszkiewicz; Kinga Kowalska-Duplaga; Tomasz Pytrus; Hanna Pituch; Andrzej Radzikowski
Background: Epidemiological and microbiological data suggest that Clostridium difficile infection (CDI) plays a substantial role in the clinical initiation of inflammatory bowel disease (IBD). The aim of the present study was to investigate the prevalence and risk factors of CDI in newly diagnosed pediatric patients with IBD. Methods: The current investigation was a retrospective study. All patients newly diagnosed with IBD in the pediatric gastroenterology clinic in Warsaw between 2007 and 2010 were included in the present study. The patients were diagnosed according to Porto criteria and microbiology evaluation screening tests for CDI were conducted. Risk factors including prior hospitalization, use of antibiotics within 2 months of CDI detection, colonic involvement, and the duration of symptoms were evaluated. CDI diagnosis was based on a positive stool enzyme immunoassay. Results: In the present study, 134 patients were evaluated (54 patients with Crohns disease, and 80 with ulcerative colitis; 87% of the patients had colonic disease). The average age of the patients was 12.3 years, and the prevalence of CDI was 47% (95% confidence interval [CI], 38%–56%). Significant differences in the prevalence of CDI between patients with Crohns disease and ulcerative colitis (P = 0.72; odds ratio [OR] = 1.187, 95% CI, 0.56–2.52) were not observed. The risk of CDI was associated with an increase in the age of the patient and the severity of the disease. Conclusions: The prevalence of CDI in newly diagnosed IBD patients was high and was independent of the type of disease. (Inflamm Bowel Dis 2011;)
Journal of Pediatric Gastroenterology and Nutrition | 2012
Tomasz Gosiewski; Magdalena Strus; Krzysztof Fyderek; Kinga Kowalska-Duplaga; Andrzej Wędrychowicz; Urszula Jedynak-Wasowicz; M. Sladek; Stanisław Pieczarkowski; Paweł Adamski; Piotr B. Heczko
Background and Aims: The commensal microbiota of the gastrointestinal tract plays an important role in the pathogenesis of inflammatory bowel disease. We examined the horizontal structure of the fecal microbiota in the colon in adolescents with Crohn disease or ulcerative colitis and a control group. Patients and Methods: Fecal samples were collected in 3 fractions from patients with Crohn disease (n = 22), ulcerative colitis (n = 12), and controls (n = 24) during preparation for colonoscopy. Additionally, biopsies from colon tissue were taken. Samples were examined using a culture technique and a fluorescent in situ hybridization method. The mucin degradation assay was carried out. Results: Quantitative composition of the microbiota was different in the consecutive 3 fecal fractions and in the colon tissue of the study groups, but in patients from the control group, the composition of microbiota in the consecutive fractions was similar. Statistical analyses showed that the total distribution of the studied bacterial taxons in the contents in all 3 fecal fractions and in the colon tissue in the given disease group, and in the control group was characteristic for the studied patient group. Differences in species distribution among the cohorts studied were highly significant (P < 0.0001). Moreover, it was shown that in the fecal fraction I and in the colon tissue samples, there is no significant difference for any of the analyzed bacterial groups, using the culture methods or fluorescent in situ hybridization, but significant results were demonstrated in the II and III fractions for specific bacterial groups. The bacterial flora attached to the mucus layer in the UC group had significantly more degraded mucus in comparison with the control group (P = 0.045). Conclusions: Distribution of the microbiota in the colon is layered, which can be called horizontal distribution of the fecal flora. Only in the ulcerative colitis group, the bacterial flora attached to the mucous layer exerts action on the mucin.
Inflammatory Bowel Diseases | 2015
Aleksandra Banaszkiewicz; Brygida Targońska; Kinga Kowalska-Duplaga; Katarzyna Karolewska-Bochenek; Agnieszka Sieczkowska; Agnieszka Gawrońska; Urszula Grzybowska-Chlebowczyk; Elżbieta Krzesiek; Izabella Łazowska-Przeorek; Maria Kotowska; Edyta Sienkiewicz; Jarosław Walkowiak; Hanna Gregorek; Andrzej Radzikowski; Piotr Albrecht
Background:There are only a few studies on immune response to pneumococcal vaccines in patients with inflammatory bowel disease (IBD); all of them assessed polysaccharide vaccines only. The aim of the study was to evaluate the immunogenicity and safety of 13-valent pneumococcal conjugate vaccine (PCV13) in IBD pediatric patients compared with healthy controls. Methods:This was a multicenter, prospective, and controlled study on children and adolescents aged 5 to 18 years with IBD with no history of pneumococcal immunization. The subjects for the study belonged to one of the following groups: patients with IBD on no immunosuppressive therapy (group A), those on tumor necrosis factor agents or immunomodulators (group B), and healthy controls (group C). The study population received 1 intramuscular injection of PCV13. The primary outcome measure was adequate vaccine response defined as postvaccination titer ≥0.35 &mgr;g/mL to all 13 serotypes. Geometric mean titers and geometric mean titer rises were measured for all serotypes. The evidence of local and systemic adverse effects for 5 days after the vaccine was registered. Results:A total of 178 subjects (122 patients and 56 controls) completed the study course. There was no significant difference in the rate of adequate vaccine response between patients with IBD and controls measured 4 to 8 weeks after vaccination (90.4% versus 96.5%, P = 0.5281). Children in group A had higher geometric mean titer rises than children in group B (P = 0.0369). There were no serious adverse events related to PCV13 during the study. Conclusions:PCV13 is both immunogenic and safe in pediatric patients with IBD.
Journal of Pediatric Gastroenterology and Nutrition | 2011
Andrzej Wędrychowicz; Kinga Kowalska-Duplaga; Urszula Jedynak-Wasowicz; Stanisław Pieczarkowski; M. Sladek; Przemyslaw Tomasik; Krzysztof Fyderek
Background and Aim: Exclusive enteral nutrition (EEN) is an effective method of treatment in achieving remission in inflammatory bowel disease (IBD); however, its mechanism of action is still poorly understood. The objective of our study was to assess the influence of EEN on serum vascular endothelial growth factor (VEGF) and transforming growth factor-beta 1 (TGF-&bgr;1) in children and adolescents with IBD. Patients and Methods: Thirty-nine children and adolescents with IBD (24 with Crohn disease [CD] and 15 with ulcerative colitis [UC]) and 25 healthy controls were enrolled in the study. VEGF and TGF-&bgr;1 were assessed at the baseline and after 2 and 4 weeks of EEN in CD and UC groups and once in controls using enzyme-linked immunosorbent assay immunoassays. Results: At the baseline, we found increased serum VEGF in the CD versus UC group and controls (P < 0.05) and serum TGF-&bgr;1 in the UC versus CD group and controls (P < 0.05). During EEN, VEGF decreased in the UC and CD groups, whereas TGF-&bgr;1 increased in the CD group and decreased in the UC group. The CD group achieved disease remission faster than the UC group, and the weight gain of patients with CD during EEN was higher compared with patients with UC. Additionally, TGF-&bgr;1 concentration correlated with protein and energies daily intake in the CD group (R = 0.95; P < 0.05). Conclusions: Different effectiveness of EEN in achieving remission in CD and UC may result from a modification of growth factor production. EEN stimulated TGF-&bgr;1 production in CD but not in UC, which possibly resulted in higher effectiveness of EEN in this group of patients.
Advances in Medical Sciences | 2016
Aleksandra Pituch-Zdanowska; Aleksandra Banaszkiewicz; Marcin Dziekiewicz; Izabella Łazowska-Przeorek; Agnieszka Gawrońska; Kinga Kowalska-Duplaga; Barbara Iwańczak; Beata Klincewicz; Urszula Grzybowska-Chlebowczyk; Jarosław Walkowiak; Piotr Albrecht
PURPOSE Determination of overweight and obesity prevalence in children with inflammatory bowel disease (IBD) at the time of diagnosis. MATERIAL AND METHODS This was a multicenter retrospective study. The study group consisted of children with new cases of IBD diagnosed in 2005-2013 according to the Porto criteria. Hospital admission records were reviewed for demographic and clinical characteristics. BMI-for-age and gender percentile charts were used to define overweight as ≥85th BMI percentile and obesity as ≥95th BMI percentile. RESULTS 675 patients were evaluated: 368 with Crohns disease (CD) and 307 with ulcerative colitis (UC). Of these, 54.8% were boys and 45.2% were girls. There were no statistically significant differences in age, weight, height and disease activity between the CD and UC patients. The UC patients had higher BMI values than the CD patients. The prevalence of overweight and obesity was higher in the UC than the CD patients (4.89% CI95 2.76-7.93 vs. 2.45% CI95 1.12-4.59 and 8.47% CI95 5.61-12.16 vs. 1.9% CI95 0.77-3.88, respectively); the differences were statistically significant (-2.44% CI95 -5.45 to 0.49 and -6.57% CI95 -10 to -3.1, respectively). The risk of overweight/obesity was 3.5 times higher for patients with UC (OR=0.272, CI95 0.14-0.49, p=0.0004). CONCLUSIONS The prevalence of overweight and obesity in newly diagnosed children with IBD was 8.4% and was higher in patients with UC than in patients with CD. The results of this study have shown that not only malnourished children may suffer from IBD but also children who are overweight or obese at the time of diagnosis.
Archives of Medical Science | 2014
Andrzej Wędrychowicz; Przemysław Tomasik; Stanisław Pieczarkowski; Kinga Kowalska-Duplaga; Zofia Grzenda-Adamek; Krzysztof Fyderek
Introduction Eosinophils contribute to the pathogenesis of inflammatory bowel disease (IBD) in the intestine. Eosinophilic cationic protein (ECP) is one of the most important eosinophilic specific mediators released during activation. The aim of the study was to evaluate the clinical value of serum ECP determination in children with active and inactive IBD and its correlation with disease activity. Material and methods There were 125 children with IBD (63 with Crohns disease – CD, 44 with ulcerative colitis – UC, 18 indeterminate colitis – IC) enrolled in the study. Among them 83 children were in the active phase of the disease, while the remaining 42 were in remission. The control group consisted of 56 healthy children. The ECP was assessed three times in children with active IBD, at baseline and after 2 and 6 weeks of treatment and once in children with inactive IBD and controls using fluoroenzymeimmunoassays. Results We found elevated ECP at baseline in the total active IBD group when compared to the inactive IBD and control groups, decreasing during treatment. Serum ECP was also elevated in the active UC and CD groups when compared to the inactive UC and CD groups, and correlated with clinical UC and CD activity (R = 0.57 and R = 0.52, p < 0.05, respectively) and duration of the clinical manifestation in UC (R = 0.62, p < 0.05) but not with the disease location in the gastrointestinal tract, or endoscopic and histopathological activity. Conclusions Evaluation of serum ECP in children with IBD may be useful in disease activity assessment at onset and during the treatment.
Gastroenterology Research and Practice | 2016
Stanisław Pieczarkowski; Kinga Kowalska-Duplaga; Przemko Kwinta; Przemysław Tomasik; Andrzej Wędrychowicz; Krzysztof Fyderek
Objectives. The aim of the study was to establish whether fecal calprotectin concentration (FCC) may be useful in children with chronic abdominal pain to differentiate between inflammatory bowel disease (IBD), other inflammatory gastrointestinal disorders, and functional gastrointestinal disorders. Methods. The study included 163 patients (median age 13 years), who were assigned to four study groups: group 0 (control), 22 healthy children; group 1, 33 children with functional gastrointestinal disorders; group 2, 71 children with inflammatory gastrointestinal disorders other than IBD; group 3, 37 children with IBD. FCC was measured using ELISA assay. Results. In group 0 and group 1 FCCs were below 100 μg/g. Low FCCs were found in 91% of patients in group 2. In patients with IBD FCCs were markedly elevated with median value of 1191.5 μg/g. However, in children with inflammatory gastrointestinal disorders other than IBD and in children with IBD mean FCCs were significantly higher compared with the control group. Significant differences in FCCs were also found between group 1 and group 2, between group 1 and group 3, and between group 2 and group 3. Conclusion. FCC is the best parameter allowing for differentiation between IBD, other inflammatory gastrointestinal disorders, and functional gastrointestinal disorders. High FCC is associated with a high probability of IBD and/or other inflammatory gastrointestinal disorders, and it allows excluding functional gastrointestinal disorders.
Archive | 2018
Kinga Kowalska-Duplaga; M. Baranowska-Nowak; M. Nescioruk; Marcin Banasiuk; Katarzyna Karolewska-Bochenek; Izabella Łazowska-Przeorek; Andrzej Radzikowski; Aleksandra Banaszkiewicz
Patients suffering from inflammatory bowel diseases (IBD) are at increased risk of infections, mainly due to immunosuppressive treatment. Moreover, infections may cause flares of IBD. Vaccination is the most effective way of preventing many infections. The aim of this study was to evaluate the vaccination status of Polish children with IBD. Individual immunization cards of children with IBD and healthy controls were reviewed. Demographic data such as age, sex, and IBD history, including therapy type, were collected. We enrolled 267 children into the study, including 214 children with IBD and 53 controls. None of the children had completed the full up-to-date routine childhood immunization schedule recommended in Poland. Controls were more than 4 times more likely to be vaccinated than the IBD patients, with the vaccines that enjoy the insurance reimbursed (OR 4.1, 95% CI 2.2-7.9). In conclusion, the study demonstrates a poor vaccination status in children suffering from IBD.
Zdrowie Publiczne i Zarządzanie | 2013
Mariusz Duplaga; Kinga Kowalska-Duplaga; Krzysztof Fyderek
Assessment of the use of information technologies among parents of children afflicted with chronic diseases Introduction and aim of the study: The support to patients with chronic conditions is an important aspect of development of e‑health systems. And yet, information about acceptance and skills related to the use of information technologies (IT) among potential end‑users is scarce. The objective of this study was assessment of the use of computer and the Internet both for general and health‑related activities in the group of parents of children suffering from chronic medical conditions. Material and methods: The survey was prepared and performed in the group of 120 parents accompanying their children during outpatient visits to speciality polyclinic (response rate 90.8%). Results: The mean age of respondents was 40.9 years; 82.6% of them were women. The use of computers was declared by 88.1% and the Internet by 80.7% of the respondents. The Internet was one of main sources of health‑related information for 77.1% of them. Checking of procedures recom‑ mended by a physician and obtaining advice from other parents were indicated most frequently among health‑related activities performed online (56,8% and 53,5% respectively). Use of the Internet depended on age, education and place of residence of respondents. These factors did not have impact on accepting of the Internet as one of the main sources of health‑related information Conclusions: The parents of children suffering from chronic conditions more frequently use IT for general and health‑related purposes than general population. Although they reveal relatively high satisfaction, there are still areas of care which could benefit from introduction of e‑health tools. How‑ ever, there are still areas which could be supported or enhanced with e‑health solutions.