Can neopterin be a useful immune biomarker for differentiating gastric intestinal metaplasia and gastric atrophy from non-atrophic non-metaplastic chronic gastritis? ¿Puede la neopterina ser un biomarcador inmunológico para diferenciar la metaplasia intestinal gástrica y la atrofia gástrica de la gastritis crónica no atrófica y no metaplásica?

Kutluana U., Kilciler A. G., MIZRAK S., Dilli U.

Gastroenterologia y Hepatologia, cilt.42, sa.5, ss.289-295, 2019 (SCI-Expanded) identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 42 Sayı: 5
  • Basım Tarihi: 2019
  • Doi Numarası: 10.1016/j.gastrohep.2019.01.005
  • Dergi Adı: Gastroenterologia y Hepatologia
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.289-295
  • Anahtar Kelimeler: C-reactive protein, Gastric atrophy, Gastric intestinal metaplasia, Helicobacter pylori, Neopterin
  • Uşak Üniversitesi Adresli: Evet

Özet

Introduction: Helicobacter pylori (H. pylori)is closely related to pre-neoplastic lesions such as gastric atrophy (GA), gastric intestinal metaplasia (GIM)and eventually gastric cancer (GC). The diagnosis of GIM and GA is usually based on endoscopic and histopathological features. Nowadays, there are no recognized good serological markers of GIM and GA. Neopterin is an important marker of cellular inflammation. In this study, we aimed to comparatively evaluate C-reactive protein (CRP)and neopterin levels in patients with GIM, GA and chronic gastritis, and to show the increased serum neopterin levels in GIM and GA according to non-atrophic and non-metaplastic chronic gastritis. Patients and methods: 98 patients with GIM and 68 patients with GA and 70 patients with non-atrophic non-metaplastic gastritis were included in the study. CRP and neopterin levels were assessed in patients and controls. Results: CRP and neopterin levels were significantly higher in patients with GIM and GA than in controls (p < 0.05 and p < 0.001, respectively). A multiple logistic regression analysis showed that high levels of serum neopterin were positively correlated with GIM and GA. According to the ROC curve analysis, the best cut-off value to differentiate between patients with GIM and/or GA from controls was ≥10.15 nmol/l (p < 0.001)for serum neopterin levels and ≥1.95 mg/l (p < 0.001)for serum CRP levels. Discussion: CRP and neopterin levels are significantly increased in GIM and GA. Neopterin may be a useful biomarker and diagnostic test for detecting GIM and GA in clinical practice. CRP levels may be helpful for this observation.