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Development of functional gastrointestinal disorders after Giardia lambliainfection
© Hanevik et al; licensee BioMed Central Ltd. 2009
Received: 20 October 2008
Accepted: 21 April 2009
Published: 21 April 2009
Functional gastrointestinal disorders (FGID) may occur following acute gastroenteritis. This long-term complication has previously not been described after infection with the non-invasive protozoan Giardia lamblia. This study aims to characterize persistent abdominal symptoms elicited by Giardia infection according to Rome II criteria and symptoms scores.
Structured interview and questionnaires 12–30 months after the onset of Giardia infection, and at least 6 months after Giardia eradication, among 82 patients with persisting abdominal symptoms elicited by the Giardia infection. All had been evaluated to exclude other causes.
We found that 66 (80.5%) of the 82 patients had symptoms consistent with irritable bowel syndrome (IBS) and 17 (24.3%) patients had functional dyspepsia (FD) according to Rome II criteria. IBS was sub classified into D-IBS (47.0%), A-IBS (45.5%) and C-IBS (7.6%). Bloating, diarrhoea and abdominal pain were reported to be most severe. Symptoms exacerbation related to specific foods were reported by 45 (57.7%) patients and to physical or mental stress by 34 (44.7%) patients.
In the presence of an IBS-subtype pattern consistent with post-infectious IBS (PI-IBS), and in the absence of any other plausible causes, we conclude that acute Giardia infection may elicit functional gastrointestinal diseases with food and stress related symptoms similar to FGID patients in general.
Long term abdominal symptoms may develop after acute gastroenteritis and was first described in 1962 . These symptoms are clinically similar to functional gastrointestinal diseases (FGID) and may be classified using the Rome II criteria for such illnesses. Symptoms often fulfil the criteria for irritable bowel syndrome (IBS) and the term post-infectious irritable bowel syndrome (PI-IBS) is often used for this condition . It has been shown to occur following viral, bacterial and amoebic gastroenteritis and after trichinellosis [1, 3, 4]. A meta-analysis found the odds of developing irritable bowel syndrome (IBS) to be increased sixfold after acute gastroenteritis . Previously, Giardia infection has been found to trigger abdominal symptoms in patients with established IBS, and Giardia should be ruled out as a possible cause in patients with IBS-like symptoms. However, post-infectious functional gastrointestinal diseases elicited by infection with the non-invasive protozoan Giardia lamblia have not been described before. Similarly, the relation of patients' abdominal symptoms and food types and the influence of physical or mental stress have been well researched among IBS-patients in general[8, 9], but little data exists regarding such relations in post-infectious FGIDs.
Giardia lamblia is a parasite of the small intestine occurring endemically, or as the cause of waterborne outbreaks. The parasite is commonly found in children in developing countries and in travellers to endemic regions. It causes infections varying from asymptomatic to protracted and severe illness with diarrhoea, weight loss and malabsorbtion. After an outbreak in autumn 2004 of assemblage B giardiasis in Bergen, Norway, many patients experienced long-lasting abdominal symptoms despite one or several courses of metronidazole. They were referred to the local university hospital for evaluation. Extensive work-up revealed a surprisingly high rate of duodenal inflammation both in patients with and without evidence of chronic infection . All Giardia positive patients were treated successfully. However, symptoms remained in many patients despite eradication of the parasite, and they were followed up regularly.
The main aim of this study was to evaluate the abdominal symptoms according to the Rome II criteria for FGID among patients with persisting abdominal symptoms 12–30 months after the onset of Giardia infection, and more than 6 months after Giardia eradication. Secondarily, we included some questions about the symptoms relation to food types and stress.
This is a prospective study describing the results of questionnaires and structured interviews during follow-up visits of patients with persisting symptoms following Giardia infection. The data were collected during a 16 month period from January 2006 until April 2007.
All 82 patients included in this study had laboratory confirmed giardiasis during an outbreak in 2004. They had been successfully treated and were confirmed Giardia negative by microscopy of three or more faecal samples at least 6 months prior to inclusion in this study. An extensive work-up including upper endoscopy with duodenal biopsies, routine blood screening tests, immunoglobulins, IgE, serum anti-endomysial, anti-tissue transglutaminase antibodies and faecal calprotectin had not produced any findings to explain their symptoms . In 11 patients included in this study, repeated routine duodenal biopsies were taken approximately one year after the initial work-up, and these were reviewed with regard to inflammatory changes.
After the initial extensive work-up, patients came for follow up visits where, in addition to routine clinical examination, a structured interview was performed with regard to previous abdominal symptoms, and symptom exacerbation related to food types or physical or mental stress. In the interview most patients denied previous abdominal illness, while 14 (17.1%) had experienced some previous abdominal symptoms. All these 14 patients reported considerable more abdominal problems after Giardia infection than they had had before. Only 5 of them reported previous contact with a physician about their abdominal problems. For clarity we chose to give results for patients without previous abdominal complaints separately in the analysis.
Patients also filled in a questionnaire regarding their current abdominal symptoms allowing evaluation of IBS according to the Rome II criteria. As it became evident that functional dyspepsia (FD) was occurring in our patient population, Rome II FD criteria questions were included in the questionnaires. IBS patients were sub classified into diarrhoea-predominant IBS (D-IBS: two or more diarrhoea symptoms and a maximum of one symptom of constipation), constipation-predominant IBS (C-IBS: two or more constipation symptoms and a maximum of one symptom of diarrhoea) and alternating IBS (A-IBS: all subjects with IBS not qualifying for D-IBS or C-IBS). Symptom severity, for the last month, of nausea, bloating, abdominal pain, diarrhoea, constipation and anorexia was quantified by patients grading these symptoms on an ordinal scale from 0 – 10 with 0 = no symptoms and 10 = severe symptoms.
Statistical analysis was performed using SPSS 16.0. The Regional ethics committee and the Norwegian Social Science Data Services approved the data collection and analysis of the data.
Frequency of FGID and relation of abdominal symptoms to food types and stress
Patients withoutprevious abdominal symptoms
N = 68
N = 82
IBS all subtypes
D – IBS1
A – IBS1
C – IBS1
IBS & FD2
Other FGID (not IBS/FD)
Food related symptoms3
Stress related symptoms4
No significant sex differences were found regarding IBS subtypes, symptom scores, influence of stress or subjective food intolerance, only trends towards more FD among females (p = 0.09) and more females reporting previous abdominal symptoms (p = 0.07). Patients with FD had similar symptom scores as non-FD patients except for the constipation score which was 2.85 in FD patients and 0.65 in non-FD patients with a p-value < 0.001.
Symptom scores in IBS subtypes and in the group with other FGIDs.
N = 31
N = 30
N = 5
N = 16
N = 82
2.8 ± 0.4
3.1 ± 0.5
3.4 ± 1.5
3.0 ± 0.8
3.0 ± 0.3
6.2 ± 0.4
7.0 ± 0.4
8.0 ± 0.8
5.4 ± 0.8
6.4 ± 0.2
3.9 ± 0.5
4.6 ± 0.4
5.2 ± 1.0
3.8 ± 0.6
4.2 ± 0.3
1.7 ± 0.5
3.1 ± 0.5
3.8 ± 1.2
0.9 ± 0.3
2.2 ± 0.3
5.4 ± 0.4
4.5 ± 0.5
3.4 ± 1.0
4.3 ± 0.7
4.8 ± 0.3
2.0 ± 0.5
1.5 ± 0.4
2.4 ± 0.8
1.1 ± 0.5
1.7 ± 0.3
22.1 ± 1.5
23.9 ± 1.6
26.2 ± 5.0
19.1 ± 2.1
22.3 ± 1.0
The question of food related worsening of symptoms was answered by 78 patients. The majority of patients (57.7%) reported their post-giardiasis abdominal problems to worsen after intake of certain food items. They were asked to name the food items they had begun to avoid. Milk and milk products were mentioned spontaneously by 27% of the patients. Other common food items mentioned were alcohol containing beverages (18.4%), wheat flour products (14.5%) and coffee (6%).
In 76 patients who responded to the question about the influence of physical or mental stress on their abdominal symptoms, 44.7% felt that their abdominal illness was worsened by stress. No correlations were found between IBS-subtypes and symptoms exacerbation related to stress and food types.
Signs of inflammation with infiltration of inflammatory cells, with or without shortening and blunting of intestinal villi, were found in 8 out of 11 of these patients during the first workup in spring 2005. One year later, repeated routine duodenal biopsies were normal in ten and improved in one of these patients, although all these patients still had troubling abdominal symptoms (data not shown).
Clinical characteristics of a relatively large number of patients seeking help for long lasting abdominal symptoms after Giardia infection are described in this study. An extensive follow-up of these patients over three years has not revealed any specific illness, which can explain the symptoms seen in our study population. The prolonged symptoms in parasitologically successfully treated patients came as a surprise, as such complications have not been described after Giardia infection before.
There have been several Giardia outbreaks described, among others in Solna, Sweden, Creston, Canada  and Aspen highlands, USA. However, no follow-up studies have looked at persistent symptoms after eradication of the parasite. An epidemiological study in Michigan, USA did not find any link between Giardia infection and IBS, by correlating new Giardia cases with prescriptions of three drugs (dicyclomine, tegaserod and alosetron) used in IBS. In our study population any such correlation would probably also not have been found as patients were previously largely healthy, active young people unaccustomed to taking drugs daily. Only a few had abdominal complaints of a severity that any of these medications would be considered.
In our study population we find a pattern of IBS-subtypes with a high frequency of diarrhoeal symptoms and little constipation. This agrees well with previous descriptions of PI-IBS as a distinctive subgroup of IBS patients . In the general population in Norway a recent study with 4622 respondents showed that 10% in the relevant age group fulfilled the IBS criteria and the pattern of subtypes contrasts our findings with subtype A-IBS most commonly reported (53%), followed by similar prevalence of the other two subtypes D-IBS (23%) and C-IBS (24%) .
It is known that Giardia may cause prolonged symptoms for several weeks after successful treatment due to secondary lactose intolerance . In the present study we found that many patients reported many different kinds of food to worsen symptoms and that this persisted for years after infection. A previous study has not found lactose-intolerance to be factor in the aetiology of PI-IBS after bacterial gastroenteritis. Preliminary data from duodenal lactase activity testing in newly referred patients with post-giardiasis IBS at our hospital support this finding (unpublished).
It is known that food-related gastrointestinal symptoms are common in the general population and often coincides with IBS. A previous study found that 51% of IBS-patient considered that their symptoms were linked to individual foods , and improvement following exclusion diets have also been reported . However, objective measurements methods, like skin prick test or intestinal permeability have not been consistent with the reported food-intolerance . Outside of this study many of the patients were referred to allergologic evaluation with no specific findings. It thus seems that the food-related symptoms seen in our patient population may be intrinsically linked with the development of FGID.
The finding that around half the patients felt that physical or mental stress influence their abdominal symptoms is consistent with previous findings in patients with IBS of all causes seeking medical care in Norway .
It remains speculative what may be the reason for development of FGID after Giardia infection. Previous studies have pointed to psychological factors, young age, and severity and duration of the acute infection as factors increasing the risk of FGID after bacterial gastroenteritis [2, 5]. We showed in a former study that a high frequency of microscopic duodenal inflammation was found in our study population when illness duration was 2–4 months, indicating that the severity of host response may be a risk factor for FGID in our population . The initially high frequency of duodenal microscopic inflammation normalised within a year, but subtle low-grade inflammation, not recognised by routine microscopy might be ongoing.
The particular genotype of Giardia responsible for the epidemic may also be a relevant risk factor in itself, as different strains have been shown to differ in their ability to induce small intestinal injury in rats . The higher proportion of females in our study population is probably not indicating an increased risk, but rather a reflection of more females contracting giardiasis during the epidemic, probably as a consequence of higher water intake . Host factors like age, no previous Giardia exposure or infection, pre-existing intestinal microbiota, immunologic and genetic predisposition may also play a role. These will be interesting issues for further research.
All patients were treated with one or more courses of metronidazole for their giardiasis. Although one study points to a link between antibiotic treatment in general and FGID, prolonged gastrointestinal symptoms is not reported as a side effect of metronidazole. Although we can not fully exclude this possibility, we think the Giardia infection is a far more plausible cause of the later FGID than its treatment.
A strength of this study is the relatively large number of laboratory confirmed giardiasis cases who have been thoroughly investigated and followed for a long period of time. However, it is therefore also important to note that our data are drawn from a population likely to be the more severely affected, and may not represent patients with milder post-giardiasis abdominal symptoms. A control group presented with the same follow-up and questionnaire would have been desirable.
Patients were asked about previous abdominal complaints retrospectively, one to two years after their Giardia infection. Recall bias might influence the answers given. Some caution should also be taken regarding the exclusion of chronic giardiasis. Microscopy of three stool samples for Giardia cysts has a sensitivity of 85 – 90%. Our patient population had repeated series of Giardia negative faecal samples before referral and during the hospital workup, thus we consider the risk of low-grade chronic infections to be very small.
Due to the subtype pattern consistent with PI-IBS, no other discernable cause, and symptoms being elicited by a symptomatic, laboratory confirmed Giardia infection, we here document for the first time that the non-invasive protozoan pathogen Giardia lamblia may induce irritable bowel syndrome and functional dyspepsia. Utilising the unique setting of around 1300 laboratory confirmed Giardia cases, we are planning follow up studies of the frequency and characteristics of FGID after Giardia infection including population based approaches.
We want to thank Per Olav Vandvik, Innlandet Hospital Health Authority, Gjøvik for valuable advice, the staff at the out-patient clinic who made this study possible and the patients who filled in forms and answered questions. This study was funded by the Medical Department, Haukeland University Hospital and by the Faculty of Medicine, University of Bergen. Data were analysed and evaluated independently by the authors, without any interference from the funding institution.
- Chaudhary NA, Truelove SC: The irritable colon syndrome. A study of the clinical features, predisposing causes, and prognosis in 130 cases. Q J Med. 1962, 31: 307-322.PubMedGoogle Scholar
- Spiller RC: Is IBS caused by infectious diarrhea?. Nat Clin Pract Gastroenterol Hepatol. 2007, 4: 642-643. 10.1038/ncpgasthep0983.View ArticlePubMedGoogle Scholar
- Marshall JK, Thabane M, Garg AX, Clark WF, Salvadori M, Collins SM: Incidence and epidemiology of irritable bowel syndrome after a large waterborne outbreak of bacterial dysentery. Gastroenterology. 2006, 131: 445-450. 10.1053/j.gastro.2006.05.053.View ArticlePubMedGoogle Scholar
- Soyturk M, Akpinar H, Gurler O, Pozio E, Sari I, Akar S, et al: Irritable bowel syndrome in persons who acquired trichinellosis. Am J Gastroenterol. 2007, 102: 1064-1069. 10.1111/j.1572-0241.2007.01084.x.View ArticlePubMedGoogle Scholar
- Thabane M, Kottachchi DT, Marshall JK: Systematic review and meta-analysis: The incidence and prognosis of post-infectious irritable bowel syndrome. Aliment Pharmacol Ther. 2007, 26: 535-544.View ArticlePubMedGoogle Scholar
- D'Anchino M, Orlando D, De Feudis L: Giardia lamblia infections become clinically evident by eliciting symptoms of irritable bowel syndrome. J Infect. 2002, 45: 169-172. 10.1016/S0163-4453(02)91038-8.View ArticlePubMedGoogle Scholar
- Grazioli B, Matera G, Laratta C, Schipani G, Guarnieri G, Spiniello E, et al: Giardia lamblia infection in patients with irritable bowel syndrome and dyspepsia: a prospective study. World J Gastroenterol. 2006, 12: 1941-1944.View ArticlePubMedPubMed CentralGoogle Scholar
- Simren M, Mansson A, Langkilde AM, Svedlund J, Abrahamsson H, Bengtsson U, et al: Food-related gastrointestinal symptoms in the irritable bowel syndrome. Digestion. 2001, 63: 108-115.View ArticlePubMedGoogle Scholar
- Vandvik PO, Wilhelmsen I, Ihlebaek C, Farup PG: Comorbidity of irritable bowel syndrome in general practice: a striking feature with clinical implications. Aliment Pharmacol Ther. 2004, 20: 1195-1203. 10.1111/j.1365-2036.2004.02250.x.View ArticlePubMedGoogle Scholar
- Ortega YR, Adam RD: Giardia: Overview and update. Clinical Infectious Diseases. 1997, 25: 545-549. 10.1086/513745.View ArticlePubMedGoogle Scholar
- Hanevik K, Hausken T, Morken MH, Strand EA, Morch K, Coll P, et al: Persisting symptoms and duodenal inflammation related to Giardia duodenalis infection. J Infect. 2007, 55: 524-530. 10.1016/j.jinf.2007.09.004.View ArticlePubMedGoogle Scholar
- Morch K, Hanevik K, Robertson LJ, Strand EA, Langeland N: Treatment-ladder and genetic characterisation of parasites in refractory giardiasis after an outbreak in Norway. J Infect. 2008, 56: 268-273. 10.1016/j.jinf.2008.01.013.View ArticlePubMedGoogle Scholar
- Thompson WG, Longstreth GF, Drossman DA, Heaton KW, Irvine EJ, Muller-Lissner SA: Functional bowel disorders and functional abdominal pain. Gut. 1999, 45 (Suppl 2): II43-II47.PubMedPubMed CentralGoogle Scholar
- Ljungstrom I, Castor B: Immune response to Giardia lamblia in a water-borne outbreak of giardiasis in Sweden. J Med Microbiol. 1992, 36: 347-352.View ArticlePubMedGoogle Scholar
- Isaac-Renton JL, Cordeiro C, Sarafis K, Shahriari H: Characterization of Giardia duodenalis isolates from a waterborne outbreak. J Infect Dis. 1993, 167: 431-440.View ArticlePubMedGoogle Scholar
- Istre GR, Dunlop TS, Gaspard GB, Hopkins RS: Waterborne giardiasis at a mountain resort: evidence for acquired immunity. Am J Public Health. 1984, 74: 602-604. 10.2105/AJPH.74.6.602.View ArticlePubMedPubMed CentralGoogle Scholar
- Penrose AS, Wells EV, Aiello AE: Infectious causation of chronic disease: examining the relationship between Giardia lamblia infection and irritable bowel syndrome. World J Gastroenterol. 2007, 13: 4574-4578.View ArticlePubMedPubMed CentralGoogle Scholar
- Dunlop SP, Jenkins D, Spiller RC: Distinctive clinical, psychological, and histological features of postinfective irritable bowel syndrome. Am J Gastroenterol. 2003, 98: 1578-1583. 10.1111/j.1572-0241.2003.07542.x.View ArticlePubMedGoogle Scholar
- Vandvik PO, Lydersen S, Farup PG: Prevalence, comorbidity and impact of irritable bowel syndrome in Norway. Scand J Gastroenterol. 2006, 41: 650-656. 10.1080/00365520500442542.View ArticlePubMedGoogle Scholar
- Farthing MJ: Giardiasis. Gastroenterol Clin North Am. 1996, 25: 493-515. 10.1016/S0889-8553(05)70260-0.View ArticlePubMedGoogle Scholar
- Parry SD, Barton JR, Welfare MR: Is lactose intolerance implicated in the development of post-infectious irritable bowel syndrome or functional diarrhoea in previously asymptomatic people?. Eur J Gastroenterol Hepatol. 2002, 14: 1225-1230. 10.1097/00042737-200211000-00010.View ArticlePubMedGoogle Scholar
- Nanda R, James R, Smith H, Dudley CR, Jewell DP: Food intolerance and the irritable bowel syndrome. Gut. 1989, 30: 1099-1104. 10.1136/gut.30.8.1099.View ArticlePubMedPubMed CentralGoogle Scholar
- Dainese R, Galliani EA, De Lazzari F, Di LV, Naccarato R: Discrepancies between reported food intolerance and sensitization test findings in irritable bowel syndrome patients. Am J Gastroenterol. 1999, 94: 1892-1897. 10.1111/j.1572-0241.1999.01226.x.View ArticlePubMedGoogle Scholar
- Cevallos A, Carnaby S, James M, Farthing JG: Small intestinal injury in a neonatal rat model of giardiasis is strain dependent. Gastroenterology. 1995, 109: 766-773. 10.1016/0016-5085(95)90383-6.View ArticlePubMedGoogle Scholar
- Nygard K, Schimmer B, Sobstad O, Walde AK, Tveit I, Langeland N, et al: A large community outbreak of waterborne giardiasis-delayed detection in a non-endemic urban area. BMC Public Health. 2006, 6: 141-10.1186/1471-2458-6-141.View ArticlePubMedPubMed CentralGoogle Scholar
- Maxwell PR, Rink E, Kumar D, Mendall MA: Antibiotics increase functional abdominal symptoms. Am J Gastroenterol. 2002, 97: 104-108. 10.1111/j.1572-0241.2002.05428.x.View ArticlePubMedGoogle Scholar
- Goka AK, Rolston DD, Mathan VI, Farthing MJ: The relative merits of faecal and duodenal juice microscopy in the diagnosis of giardiasis. Trans R Soc Trop Med Hyg. 1990, 84: 66-67. 10.1016/0035-9203(90)90386-S.View ArticlePubMedGoogle Scholar
- The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-230X/9/27/prepub
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