2022
DOI: 10.1016/j.amsu.2022.103844
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Serum pepsinogen: A potential non-invasive screening method for moderate and severe atrophic gastritis among an asian population

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Cited by 4 publications
(7 citation statements)
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References 28 publications
(43 reference statements)
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“…The diagnostic value of PG testing has been assessed in several studies using different methods (enzyme-linked immunosorbent assay, ELISA; Chemiluminescent Immunoassay, CLEIA), with a different cut-off value for each method and adjusted for different population/ethnicity [30][31][32][33][34][35][36][37][38] (Table 1). The role of PG serology in atrophic gastritis has been underlined in several international recommendations: MAPS I and II consensus stated that serum pepsinogen levels can predict extensive CAG.…”
Section: Blood Biomarkers 131 Validated and Commercially Available Bi...mentioning
confidence: 99%
See 2 more Smart Citations
“…The diagnostic value of PG testing has been assessed in several studies using different methods (enzyme-linked immunosorbent assay, ELISA; Chemiluminescent Immunoassay, CLEIA), with a different cut-off value for each method and adjusted for different population/ethnicity [30][31][32][33][34][35][36][37][38] (Table 1). The role of PG serology in atrophic gastritis has been underlined in several international recommendations: MAPS I and II consensus stated that serum pepsinogen levels can predict extensive CAG.…”
Section: Blood Biomarkers 131 Validated and Commercially Available Bi...mentioning
confidence: 99%
“…Presented outcomes reflect a diagnosis of CAG based on histopathological examination. Still, PGI and PGI/II also showed similar outcomes in the endoscopic diagnosis of atrophy using the Kimura–Takemoto classification [ 32 , 37 , 39 ]. Also, PG testing is effective in the prediction of atrophy based on the origin of gastritis.…”
Section: Introductionmentioning
confidence: 98%
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“…Currently, biomarkers including CEA, CA19‐9, and CA72‐4 are frequently utilized in the detection of patients with GC, although their diagnosis is somewhat limited due to their low sensitivity or specificity 3 . Additionally, PG I, PG II, and PG I/II have less usefulness in the diagnosis of GC 4 . Finding new biomarkers for the early diagnosis, therapy, and prognostic evaluation of GC becomes critical and necessary.…”
Section: Introductionmentioning
confidence: 99%
“… 3 Additionally, PG I, PG II, and PG I/II have less usefulness in the diagnosis of GC. 4 Finding new biomarkers for the early diagnosis, therapy, and prognostic evaluation of GC becomes critical and necessary.…”
Section: Introductionmentioning
confidence: 99%