Marco Valvano, Chiara Giansante, Antonio Vinci, Massimo Maurici, Stefano Fabiani, Gianpiero Stefanelli, Nicola Cesaro, Angelo Viscido, Claudia Caloisi, Giovanni Latella
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引用次数: 0
Abstract
Background: The main treatment for Celiac Disease (CD) is the gluten-free diet (GFD). However, in some CD patients, iron deficiency anemia can be persistent despite a GFD.
Aim: In this study, we aim to evaluate the prevalence of anemia in both adults and children with CD at the diagnosis and during the GFD.
Methods: In this cross-sectional study including both adults and children with CD, the demographic characteristics and hemoglobin, iron, folate and vitamin B12 levels were retrospectively retrieved from patients' medical records at the time of diagnosis (T0); after 3-5 years (T1) and after 8-10 years (T2) of GFD.
Results: 311 CD patients (184 adults and 127 pediatric patients) were included in the study. No difference was observed in the prevalence of anemia in the overall population after 3-5 years of GFD in both adult and pediatric patients compared to the diagnosis. At 8-10 years, in the adult patient's group, a significant reduction in the prevalence of anemia was observed (24% vs. 17.8% p = 0.043).
Conclusions: Despite the GFD and a very long observational period the diagnosis of anemia persists in 17.8% and 4.4% of adult and pediatric patients, respectively. The diagnostic delay (longer in adult patients) and a more pronounced ultrastructural mucosal injury could play a role in the persistence of anemia despite the GFD.
背景:乳糜泻(CD)的主要治疗方法是无麸质饮食(GFD)。然而,在一些乳糜泻患者中,尽管有GFD,缺铁性贫血仍可能持续存在。目的:在本研究中,我们旨在评估成人和儿童乳糜泻在诊断时和GFD期间贫血的患病率。方法:在这项横断面研究中,包括成人和儿童的CD,回顾性地从患者诊断时的医疗记录中检索人口统计学特征和血红蛋白、铁、叶酸和维生素B12水平(T0);3-5年(T1)和8-10年(T2)。结果:311例CD患者(184例成人和127例儿科患者)纳入研究。与诊断相比,在成人和儿童GFD患者3-5年后,总体人群中贫血的患病率没有差异。在8-10年,在成人患者组中,观察到贫血患病率显著降低(24%对17.8% p = 0.043)。结论:尽管有GFD和很长的观察期,17.8%和4.4%的成人和儿童患者仍然诊断为贫血。诊断延迟(成人患者较长)和更明显的超微结构粘膜损伤可能在GFD后持续贫血中发挥作用。
期刊介绍:
BMC Gastroenterology is an open access, peer-reviewed journal that considers articles on all aspects of the prevention, diagnosis and management of gastrointestinal and hepatobiliary disorders, as well as related molecular genetics, pathophysiology, and epidemiology.