TY - JOUR
T1 - Increased risk of irritable bowel syndrome in university students due to gastrointestinal symptom-specific anxiety
AU - Saigo, Tatsuo
AU - Tayama, Jun
AU - Ogawa, Sayaka
AU - Bernick, Peter J.
AU - Takeoka, Atsushi
AU - Hayashida, Masaki
AU - Shirabe, Susumu
N1 - Funding Information:
We would like to express our gratitude to the participants of the present study. This study was supported by the Center for Health and Community Medicine at Nagasaki University and the Japan Society for the Promotion of Science (JSPS) KAKENHI (Grant Number 15K21234).
Publisher Copyright:
© 2018, Nagasaki University School of Medicine. All rights reserved.
PY - 2018/3
Y1 - 2018/3
N2 - Background: Gastrointestinal symptom-specific anxiety (GSA) has been reported to impact symptom severity in irritable bowel syndrome (IBS), suggesting that GSA may be an important treatment outcome. The present study explored whether higher levels of GSA were associated with increased risk of having IBS, and whether individuals with IBS were at greater risk for severe gastrointestinal (GI) symptoms. Methods: Participants comprised 1156 university students. The Rome III modular questionnaire was used to assess for IBS. GSA was measured using the Japanese version of the Visceral Sensitivity Index (VSI). IBS-SI was used to assess severity of GI symptoms. Data were analyzed using univariate and multivariate logistic regression analysis. Results: The prevalence rate of IBS (provisional diagnosis, based on Rome III questionnaire responses) was 21%. Logistic regression analysis was performed using the VSI cutoff point as the independent variable, and the presence or absence of IBS as the dependent variable. Results indicate that for individuals above the VSI cutoff point, the adjusted odds ratio for having IBS was 2.64 (95% CI: 1.87-3.71). Furthermore, results indicate that in participants with high GSA, adjusted odds ratios for severity of IBS symptoms were 0.44 (95% CI: 0.33-0.58) for subclinical, 1.15 (95% CI: 0.90–1.46) for mild symptoms, 2.19 (95% CI: 1.57–3.07) for moderate symptoms, and 5.63 (95% CI: 2.24–14.15) for severe symptoms. Conclusion: Higher VSI scores were associated with having risk factors for IBS and greater severity of IBS symptoms.
AB - Background: Gastrointestinal symptom-specific anxiety (GSA) has been reported to impact symptom severity in irritable bowel syndrome (IBS), suggesting that GSA may be an important treatment outcome. The present study explored whether higher levels of GSA were associated with increased risk of having IBS, and whether individuals with IBS were at greater risk for severe gastrointestinal (GI) symptoms. Methods: Participants comprised 1156 university students. The Rome III modular questionnaire was used to assess for IBS. GSA was measured using the Japanese version of the Visceral Sensitivity Index (VSI). IBS-SI was used to assess severity of GI symptoms. Data were analyzed using univariate and multivariate logistic regression analysis. Results: The prevalence rate of IBS (provisional diagnosis, based on Rome III questionnaire responses) was 21%. Logistic regression analysis was performed using the VSI cutoff point as the independent variable, and the presence or absence of IBS as the dependent variable. Results indicate that for individuals above the VSI cutoff point, the adjusted odds ratio for having IBS was 2.64 (95% CI: 1.87-3.71). Furthermore, results indicate that in participants with high GSA, adjusted odds ratios for severity of IBS symptoms were 0.44 (95% CI: 0.33-0.58) for subclinical, 1.15 (95% CI: 0.90–1.46) for mild symptoms, 2.19 (95% CI: 1.57–3.07) for moderate symptoms, and 5.63 (95% CI: 2.24–14.15) for severe symptoms. Conclusion: Higher VSI scores were associated with having risk factors for IBS and greater severity of IBS symptoms.
KW - Gastrointestinal symptom-specific anxiety
KW - Irritable bowel syndrome
KW - Visceral sensitivity index
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M3 - Article
AN - SCOPUS:85048536312
SN - 0001-6055
VL - 61
SP - 137
EP - 143
JO - Acta Medica Nagasakiensia
JF - Acta Medica Nagasakiensia
IS - 4
ER -