S3097 Combined Oral Contraceptives Are Associated With Increased Risk of Developing Small Intestinal Bacterial Overgrowth in Pre-Menopausal Women

Introduction: SIBO disproportionately affects women. Sex hormones may influence the higher prevalence of SIBO in women. This study investigated the effects of combined oral contraceptives (COC) on SIBO and its related symptoms, medication use, and diagnostic testing in pre-menopausal women. Methods: Utilizing the TriNetX platform, we conducted a large population-based cohort study involving pre-menopausal women aged 18-49, with and without COC (estrogen and progesterone). 1:1 propensity score matching was performed to adjust for age, race, and ethnicity. Exclusion criteria included International Classification of Diseases codes for menopause, ulcerative colitis, Crohn’s, diabetes, irritable bowel syndrome, proton pump inhibitor usage, gastroparesis, lactose intolerance, functional dyspepsia, pancreatic insufficiency, liver disease, intestinal pseudo-obstruction, adhesions, connective tissue disorders, opiate use, intestinal malignant neoplasms, bariatric and surgical procedures. Odds ratios with 95% confidence intervals were calculated. Results: After applying exclusion criteria, we identified 1,443,477 pre-menopausal women prescribed COC and 11,929,503 not prescribed COC. Post-propensity matching, each cohort comprised 1,421,461 patients. 239 pre-menopausal women prescribed COC developed SIBO at least 30 days after being prescribed COC compared to 96 pre-menopausal women not prescribed COC (OR = 2.49, 95% CI [1.96-3.15]). These associations persisted in sensitivity analysis over 3 years (OR = 1.56 95% CI [1.16-2.28]). COC were associated with increased GI symptoms including abdominal pain (OR = 2.11 95% CI [2.06-2.16]), gas pain (OR = 2.98 95% CI [2.79-3.18]), abdominal distention (OR = 3.02 95% CI [2.93-3.12]), flatulence (OR = 2.84 95% CI [2.67-3.03]), intestinal malabsorption (OR = 1.94 95% CI [1.85-2.04]), abnormal weight loss (OR = 2.92 95% CI [2.83-3.01]), diarrhea (OR = 2.21 95% CI [2.17-2.25]), and b12 deficiency (OR = 2.16 95% CI [1.97-2.37]). Medications including rifaximin (OR = 3.53 95% CI [3.12-4.01]) and neomycin (OR = 2.25 95% CI [2.19-2.32]) were more likely to be prescribed in pre-menopausal women on COC. Colonoscopy (OR = 2.28 95% CI[1.65-3.15]), and hydrogen/methane breath test (OR 1.79 95% CI [1.58-2.02]) were more likely to be performed in pre-menopausal women prescribed COC. Conclusion: Our study reveals a compelling association between COC and an increased risk of developing SIBO, which persists overtime. Additionally, COC are correlated with elevated gastrointestinal symptoms, augmented medication utilization, and heightened diagnostic testing commonly seen in patients with SIBO.

Publication Details

Journal
The American Journal of Gastroenterology
Published
2025-10-01
DOI
https://doi.org/10.14309/01.ajg.0001139848.32641.e9
Primary Topic
Inflammatory Bowel Disease
Type
article
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article

S3097 Combined Oral Contraceptives Are Associated With Increased Risk of Developing Small Intestinal Bacterial Overgrowth in Pre-Menopausal Women

The American Journal of Gastroenterology
Inflammatory Bowel Disease
article

S3097 Combined Oral Contraceptives Are Associated With Increased Risk of Developing Small Intestinal Bacterial Overgrowth in Pre-Menopausal Women

article en

Abstract

Introduction: SIBO disproportionately affects women. Sex hormones may influence the higher prevalence of SIBO in women. This study investigated the effects of combined oral contraceptives (COC) on SIBO and its related symptoms, medication use, and diagnostic testing in pre-menopausal women. Methods: Utilizing the TriNetX platform, we conducted a large population-based cohort study involving pre-menopausal women aged 18-49, with and without COC (estrogen and progesterone). 1:1 propensity score matching was performed to adjust for age, race, and ethnicity. Exclusion criteria included International Classification of Diseases codes for menopause, ulcerative colitis, Crohn’s, diabetes, irritable bowel syndrome, proton pump inhibitor usage, gastroparesis, lactose intolerance, functional dyspepsia, pancreatic insufficiency, liver disease, intestinal pseudo-obstruction, adhesions, connective tissue disorders, opiate use, intestinal malignant neoplasms, bariatric and surgical procedures. Odds ratios with 95% confidence intervals were calculated. Results: After applying exclusion criteria, we identified 1,443,477 pre-menopausal women prescribed COC and 11,929,503 not prescribed COC. Post-propensity matching, each cohort comprised 1,421,461 patients. 239 pre-menopausal women prescribed COC developed SIBO at least 30 days after being prescribed COC compared to 96 pre-menopausal women not prescribed COC (OR = 2.49, 95% CI [1.96-3.15]). These associations persisted in sensitivity analysis over 3 years (OR = 1.56 95% CI [1.16-2.28]). COC were associated with increased GI symptoms including abdominal pain (OR = 2.11 95% CI [2.06-2.16]), gas pain (OR = 2.98 95% CI [2.79-3.18]), abdominal distention (OR = 3.02 95% CI [2.93-3.12]), flatulence (OR = 2.84 95% CI [2.67-3.03]), intestinal malabsorption (OR = 1.94 95% CI [1.85-2.04]), abnormal weight loss (OR = 2.92 95% CI [2.83-3.01]), diarrhea (OR = 2.21 95% CI [2.17-2.25]), and b12 deficiency (OR = 2.16 95% CI [1.97-2.37]). Medications including rifaximin (OR = 3.53 95% CI [3.12-4.01]) and neomycin (OR = 2.25 95% CI [2.19-2.32]) were more likely to be prescribed in pre-menopausal women on COC. Colonoscopy (OR = 2.28 95% CI[1.65-3.15]), and hydrogen/methane breath test (OR 1.79 95% CI [1.58-2.02]) were more likely to be performed in pre-menopausal women prescribed COC. Conclusion: Our study reveals a compelling association between COC and an increased risk of developing SIBO, which persists overtime. Additionally, COC are correlated with elevated gastrointestinal symptoms, augmented medication utilization, and heightened diagnostic testing commonly seen in patients with SIBO.

The American Journal of GastroenterologyVol. 120(10S2)
Good health and well-being
Openalex Percentile: Top 27%
Inflammatory Bowel Disease
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