The DOI matches its Crossref record; 32 of the 32 references it cites were found in a registry or an index.
Distinctive Clinical, Psychological, and Histological Features of Postinfective Irritable Bowel Syndrome
Abstract
OBJECTIVE: Irritable bowel syndrome after gastroenteritis is well recognized. Our aim was to determine whether postinfective IBS (PI-IBS) has histological or clinical features that are distinct from those of IBS patients with no history of preceding infection. METHODS: A total of 75 consecutive IBS outpatients and 36 healthy control subjects completed a questionnaire detailing symptoms, mode of onset, and previous psychiatric history. All underwent a full diagnostic workup including rectal biopsy, which included immunostaining and quantification for lamina propria or intraepithelial T lymphocytes, serotonin-containing enterochromaffin (EC), and mast cells. Patients were divided according to onset of symptoms into PI-IBS (n = 23) or non-PI-IBS (n = 52) patients. RESULTS: Diarrhea predominance occurred more frequently in PI-IBS (70%) than in non-PI-IBS (42%) patients (p = 0.03). A history of previous treatment for anxiety or depression was present in 26% of PI-IBS patients compared to 54% of non-PI-IBS (p = 0.02). Biopsy results for all patients were normal using conventional criteria; however, quantification revealed that PI-IBS showed increased EC cells compared to those of non-PI-IBS patients (p = 0.017) and controls (p = 0.02). Lamina propria T lymphocytes were increased in PI-IBS (p = 0.026) and non-PI-IBS (p = 0.011) patients compared to controls. Mast cells were increased in non-PI-IBS patients (p = 0.054) compared to controls. CONCLUSIONS: Individuals with PI-IBS are a clinically distinct subgroup characterized by diarrheal symptoms, less psychiatric illness, and increased serotonin-containing EC cells compared to those with non-PI-IBS.
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In the citing paper
“Other investigators have reported increased gastrointestinal permeability and elevated immune cell counts, even in patients with IBS without an infective aetiology. 54,55”
From Irritable bowel syndrome (2020) · cites this paper as [55]
In the citing paper
“Additionally, increased concentrations of CD3+ T cells in the colon and rectum and in the myenteric plexus of the small intestine were increased in these patients compared with normal controls (36, 46, 57, 58, 89, 94, 133, 168, 174).”
From Intestinal microbiota and immune function in the pathogenesis of irritable bowel syndrome (2013) · cites this paper as [58]
In the citing paper
“However, as with mast cells, IELs are not consistently elevated in IBS patients (57, 58, 133).”
From Intestinal microbiota and immune function in the pathogenesis of irritable bowel syndrome (2013) · cites this paper as [58]
In the citing paper
“However, some studies failed to demonstrate increased activated mast cells in IBS patients (35, 36, 57, 58, 168) and there are no consistent differences in the tissue concentrations of activated mast cells in patients with different IBS subtypes (36, 189).”
From Intestinal microbiota and immune function in the pathogenesis of irritable bowel syndrome (2013) · cites this paper as [58]
In the citing paper
“The importance of the interaction between the intestinal microbiota and immune system in IBS patients is demonstrated by a few studies in patients with PI-IBS, indicating activation of the GI immune system following the acute GI infection (57, 58, 75, 89, 94, 124, 168, 170, 187)”
From Intestinal microbiota and immune function in the pathogenesis of irritable bowel syndrome (2013) · cites this paper as [58]
In the citing paper
“The evidence from these in vitro studies may shed light on the reported association of stressful life events with the duration of gastroenteritis, and with the subsequent development of postinfectious IBS.37”
From Principles and clinical implications of the brain-gut-enteric microbiota axis (2009) · cites this paper as [37]
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Chronic Complications After Travelers' Diarrhea
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Tuteja, A. K., Leung, D. T., Fang, J. C., Talley, N. J., & Stoddard, G. J. (2024) · Neurogastroenterology & Motility · doi:10.1111/nmo.14889 · Cited by 5
Blackshaw, L. A., Brierley, S. M., Harrington, A. M., & Hughes, P. A. (2013) · The Open Pain Journal · doi:10.2174/1876386301306010023 · Cited by 4
“Allodynia and hyperalgesia to mechanical events like distension and contraction are hallmarks of chronic visceral pains [88-90], along with inflammation, which may be very low-grade histologically [91-93].”
BackgroundParasitosis y síndrome de intestino irritable
Ibarra, C. C., Herrera, V., de Arce, E. P., Gil, L. C., Madrid, A. M., Valenzuela-Pérez, L., & Beltrán, C. J. (2016) · Revista chilena de infectología · doi:10.4067/s0716-10182016000300003 · Cited by 4
Irritable Bowel Syndrome Onset after New Coronavirus Infection COVID-19
Feklina, I. Y., Mnatsakanyan, M. G., Павлович, П. А., & Валерьевна, Т. О. (2022) · Russian Journal of Gastroenterology Hepatology Coloproctology · doi:10.22416/1382-4376-2021-31-6-23-28 · Cited by 4
“сообщают о СРК-З менее чем в 10 % случаев [10].”
The Relationship of Enteric Microbial Infection and Functional Bowel Disorders
Collins, S. (2007) · Journal of Clinical Gastroenterology · doi:10.1097/mcg.0b013e31802db351 · Cited by 6
Role of antispasmodics in the treatment of irritable bowel syndrome
Drozdov, V., Arefev, K. I., Serebrova, S., Komissarenko, I., Shikh, E., & Starodubtsev, A. K. (2021) · Meditsinskiy sovet = Medical Council · doi:10.21518/2079-701x-2021-5-155-164 · Cited by 1
The evolution of irritable bowel syndrome as a group of organic diseases: a narrative review
Saidara, E., Barlow, G. M., & Pimentel, M. (2025) · Expert Review of Gastroenterology & Hepatology · doi:10.1080/17474124.2025.2549381 · Cited by 3
“Some studies have found mast cell hyperplasia to be more common in IBS-D, and others found it not to be related to PI-IBS [139–141].”
Duan, S., Kanda, H., Zhu, F., Okubo, M., Koike, T., Ohno, Y., Tanaka, T., Harima, Y., Miyamichi, K., Fukui, H., et al. (2025) · Cellular and Molecular Gastroenterology and Hepatology · doi:10.1016/j.jcmgh.2025.101658 · Cited by 4
Trastornos funcionales digestivos post-infecciosos: del episodio agudo a la molestia crónica
Mearin, F., & Balboa, A. (2011) · Gastroenterología y Hepatología · doi:10.1016/j.gastrohep.2011.03.016 · Cited by 3
Pathophysiological approach to chronic diarrhoea
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Hicks, G. A. (2007) · Elsevier eBooks · doi:10.1016/b0-08-045044-x/00283-2 · Cited by 3
Acuña, R. (2015) · Revista Médica Clínica Las Condes · doi:10.1016/j.rmclc.2015.09.010 · Cited by 3
Blackett, J. W., Elkind, M. S. V., O’Byrne, S. M., Wainberg, M. L., Purpura, L. J., Chang, L., & Freedberg, D. E. (2023) · Gastro Hep Advances · doi:10.1016/j.gastha.2023.06.006 · Cited by 3
“It is well-known that chronic GI symptoms can develop in response to infections of the digestive tract, a phenomenon known as postinfection IBS 7 – 10 and approximately 10% of patients meet criteria for IBS after a diagnosis of infectious enteritis.”
BackgroundNeuropathophysiology of the Irritable Bowel Syndrome
Wood, J. D. (2018) · Elsevier eBooks · doi:10.1016/b978-0-12-809954-4.00067-0 · Cited by 3
Functional abdominal pain disorders and asthma: two disorders, but similar pathophysiology?
Kumari, M. V., Amarasiri, L., Rajindrajith, S., & Devanarayana, N. M. (2020) · Expert Review of Gastroenterology & Hepatology · doi:10.1080/17474124.2020.1821652 · Cited by 3
Mindfulness for the Treatment of Stress Disorders
Pallesen, K. J., Dahlgaard, J., & Fjorback, L. O. (2015) · Springer eBooks · doi:10.1007/978-3-319-22255-4_8 · Cited by 3
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Etiology and pathophysiology of irritable bowel syndrome and chronic constipation
Camilleri, M. (2005) · Advanced studies in medicine · Cited by 3
Immune activation in irritable bowel syndrome: from basic to clinic
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Chronic symptoms persisting after travel-related infections
Bogacka, A., & Gajewski, M. (2018) · International Maritime Health · doi:10.5603/imh.2018.0033 · Cited by 4
“PI-IBS is diagnosed according to the Rome IV criteria, with the additional criterion of onset following an acute infectious gastroenteritis characterised by two or more symptoms such as fever, vomiting, diarrhoea, and a positive stool culture result [14, 15].”
MethodTalley, N. J. (2010) · Elsevier eBooks · doi:10.1016/b978-1-4160-6189-2.00118-9 · Cited by 3
PATHOPHYSIOLOGICAL FACTORS OF IRRITABLE BOWEL SYNDROME, AND THE EFFECTS OF PROBIOTIC SUPPLEMENTATION
Kajander, K. (2008) · Työväentutkimus Vuosikirja · Cited by 3
Michail, S. K. (2009) · Humana Press eBooks · doi:10.1007/978-1-60327-289-6_10 · Cited by 3
Psychiatric Disease and Functional GI Disorders in the Community: More Evidence for a Casual Link?
Locke, G. R., Lin, S.-C., & Talley, N. J. (2005) · The American Journal of Gastroenterology · doi:10.1111/j.1572-0241.2005.41277_3.x · Cited by 3
Moyer, M. B. L., & Shenk, M. K. (2025) · American Journal of Biological Anthropology · doi:10.1002/ajpa.70104 · Cited by 3
“Another, separate causal trajectory of IBS may be post-infectious in origin, resulting as a downstream health concern from bacterial gastrointestinal illnesses (Dunlop et al. 2003).”
Metadata
- Authors
- Dunlop, S. P., Jenkins, D., & Spiller, R. C.
- Affiliations
- Nottingham University Hospitals NHS Trust (GB)
- ORCID
- Jenkins, David
- Venue
- American Journal of Gastroenterology
- Published
- 2003-07
- Volume
- 98
- Issue
- 7
- Pages
- 1578-1583
- ISSN
- 0002-9270 (ISSN-L)
- OpenAlex
- W2033889517
- Cited by
- 359
- References
- 32
- Citations by year
- 2026: 1 · 2025: 6 · 2024: 4 · 2023: 6 · 2022: 6 · 2021: 5 · 2020: 10 · 2019: 9 · 2018: 14 · 2017: 13 · 2016: 17 · 2015: 14 · 2014: 28 · 2013: 24 · 2012: 23
- FWCI
- 12.90
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- The American Journal of Gastroenterology (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Gastroenterology › Gastrointestinal motility and disorders
- Health Sciences › Medicine › Gastroenterology › Microscopic Colitis
- Health Sciences › Medicine › Gastroenterology › Inflammatory Bowel Disease
- Keywords
- irritable bowel syndrome, gastroenteritis, rectal biopsy, enterochromaffin cells, serotonin, mast cells, diarrhea, psychiatric comorbidity, anxiety, depression, immunohistochemistry
- MeSH terms
- Adult, Mental Disorders, Biopsy, Cell Count, Colonic Diseases, Functional, Diarrhea, Enterochromaffin Cells, Female, Gastroenteritis, Humans, Immunohistochemistry, Male, Mast Cells, Middle Aged, Rectum, Serotonin, T-Lymphocytes
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