TY - JOUR T1 - Çölyak hastalarında ve sağlıklı çocuklarda laktoz malabsorbsiyonu TT - Lactose malabsorption in children with celiac disease and healthy children AU - Comba, Atakan AU - Demirbaş, Fatma AU - Eren, Esra AU - Çaltepe, Gönül AU - Yüce, Özlem AU - Kalaycı, Ayhan Gazi PY - 2019 DA - May Y2 - 2019 DO - 10.31362/patd.531821 JF - Pamukkale Medical Journal JO - Pam Med J PB - Pamukkale University WT - DergiPark SN - 1308-0865 SP - 321 EP - 328 VL - 12 IS - 2 LA - tr AB - Amaç Laktoz malabsorbsiyonu, doğuştan, primer veyasekonder olarak ortaya çıkabilir. Çölyak hastalığı, sekonder laktozmalabsorbsiyona neden olan birhastalıktır. Bu çalışmada, çölyak hastası çocuklar ile sağlıklıçocuklarda laktoz hidrojen nefes testi ile laktoz malabsorbsiyon sıklığınınbelirlenmesi amaçlanmıştır.Gereçve Yöntem Çalışmaya, 64 çölyakhastası ve 52 sağlıklı çocuk dahil edildi. Çölyak hastaları yeni tanı alanlarve takipli çölyak hastaları olarak iki gruba ayrıldı. Takipli çölyak hastaları tedaviye(glutensiz diyete) tam uyumlu olanlar ve tedaviye uyumsuz olanlar olarak ikigrupta incelendi. Laktoz hidrojen nefes testi 0-500 ppm hidrojen seviyesinialgılayabilen ve 1 ppm düzeyinde duyarlı gaz analiz cihazı kullanılarakyapıldı. BulgularÇocukların ortalama yaşı 10,4 ±4,5 yıldı. Çölyak hastalarının 16’sıyeni tanılı, 48’i takipli idi. Takipli çölyakların 24’ü (%50) glutensiz diyetetam uyumluydu. Yeni tanı çölyak hastalarının %62,5’inde, glutensiz diyeteuyumsuz olanların %54,2’sinde, glutensiz diyete tam uyumluların %33,3’ünde,sağlıklı çocukların ise %19,2’sinde laktoz hidrojen nefes testi pozitifti. Yenitanılı ve glutensiz diyete uymayan çölyak hastalarının laktoz hidrojen nefestesti pozitiflik oranı (sırasıyla, %62,5; %54,2), sağlıklı çocuklardan (%19,2)anlamlı olarak yüksekti (sırasıyla, p=0,002ve p=0,003). Hem çölyak hastalarındahem de sağlıklı çocuklarda, laktoz hidrojen nefes testi pozitif olanların bedenkitle indeksi z skoru, negatif olan çocuklardan anlamlı olarak düşüktü (p<0,001,p=0,041; sırasıyla).SonuçÇalışmada, çölyak serolojisi pozitif olan hastalarda laktoz hidrojen nefestesti pozitifliği anlamlı olarak yüksek bulundu. Çölyak hastalığında laktozhidrojen nefes testi ile laktoz malabsorbsiyon sıklığı ve mukozal hasarindirekt olarak saptanabilir. Laktoz malabsorbsiyonu, beden kitle indeksi düşükolan çocuklarda daha sık görülmektedir. KW - çocuk KW - çölyak hastalığı KW - hidrojen nefes testi KW - laktoz malabsorbsiyonu N2 - Purpose.Lactose malabsorption(LM) can be congenital, primary, or secondary. Celiacdisease (CD) is a secondary cause of lactose malabsorption. This study aimed todetermine lactose malabsorption frequency using a lactose hydrogen breath test(LHBT) in children with celiac disease and healthy children. Materials and methods.The study included 64 children with CD and 52 healthy controls. Celiac patients were dividedinto groups as newly diagnosed and followed celiac patients. The latter weredivided into groups as compliance or noncompliance with gluten-free diet (GFD).LHBT was performed using a gas analyser with a1-ppm sensor sensitivity of hydrogen levels of 0–500 ppm.Results.Mean age of thechildren was 10.4 ± 4.5 years. Sixteen of the patients had newly diagnosedceliac disease, and 24 (50%) were compliant with GFD. LHBT results were positive in 62.5% of the newly diagnosed CDpatients, 33.3% of those compliant with GFD,54.2% of those non-compliant with GFD,and 19.2% of controls. Asignificantly higher proportion of newly diagnosed CD (62.5%) and non-compliantwith GFD (54.2%) had positive LHBTresults than controls (19.2%) (p=0.002and p=0.003, respectively). The body mass index z scores of the childrenwith LHBT positivity were significantly lower than others in both healthychildren and children with CD (p<0.001,p=0.041, respectively).Conclusion.In our study, the frequency of LHBT positivity was significantly higher inceliac patients with positive celiac serology.LHBTidentified mucosal damage as indirect in celiac disease. Lactose malabsorptionis more common in children who have low body mass index. CR - Kaynaklar1. Guandalini S, Setty M. Celiac disease. Curr Opin Gastroenterol 2008;24:707-712. doi: 10.1097/MOG.0b013e32830f4527.2. Kang JY, Kang AH, Green A, Gwee KA, Ho KY. Systematic review: Worldwide variation in the frequency of celiac disease and changes over time. Aliment Pharmacol Ther 2013;38:226-245. doi: 10.1111/apt.12373.3. Lionetti E, Catassi C. New clues in celiac disease epidemiology, pathogenesis, clinical manifestations, and treatment. Int Rev Immunol 2011;30:219-231. doi: 10.3109/08830185.2011.602443.4. 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UR - https://doi.org/10.31362/patd.531821 L1 - https://dergipark.org.tr/en/download/article-file/725442 ER -