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The intrinsic fluorescence spectrum of dilute gastric juice as a novel diagnostic tool for gastric cancer
Author(s) -
ZHOU Li Ya,
LIN San Ren,
LI Yuan,
GENG Qiu Ming,
DING Shi Gang,
MENG Ling Mei,
SUN Xiao Ning,
WANG Jing Tong,
XU Zhi Jie,
GUO Hui Lan,
LI Cheng Gang,
CUI Rong Li
Publication year - 2011
Publication title -
journal of digestive diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.684
H-Index - 51
eISSN - 1751-2980
pISSN - 1751-2972
DOI - 10.1111/j.1751-2980.2011.00507.x
Subject(s) - cancer , medicine , fluorescence , receiver operating characteristic , excitation wavelength , gastroenterology , stomach , nuclear medicine , pathology , physics , quantum mechanics
OBJECTIVE: To investigate the intrinsic fluorescence spectrum of gastric juice as a diagnostic method for gastric cancer. METHODS: We collected gastric juice by gastroscopy in 1870 patients from May 2001 to March 2006, of whom 202 were involved in a preliminary test, 162 in experimental optimization and 1506 in clinical verification. The best dilution and pH value were chosen in the experimental optimization phase. Clinical verification was based on optimized samples. Intrinsic fluorescence spectra were measured in all samples with a fluorescence spectrophotometer using an excitation wavelength of 288 nm. RESULTS: The first peak of fluorescence intensity (P 1 FI) of the intrinsic fluorescence spectrum was significantly higher in gastric juice from patients with gastric cancer than from those with benign lesions. There was no significant difference in the P 1 FI differences between patients with benign and malignant lesions with samples diluted by 20‐fold to 80‐fold and from pH 9 to pH 11. Clinical verification in 1506 patients showed that P 1 FI ≥ 76.5 was the optimal cut‐off on the receiver operating characteristic curve for diagnosing gastric cancers: sensitivity was 83.2%, specificity 80.7% and accuracy 82.0%. CONCLUSIONS: P 1 FI of the intrinsic fluorescence at 288 nm is significantly higher in patients with gastric cancers than in individuals with benign lesions. As a clinical indicator of gastric cancer, its sensitivity, specificity and accuracy were high.