5HTTLPR polymorphism of serotonin transporter yields short (S) and long (L) alleles. SS and LS genotypes are associated with reduced expression of serotonin transporter. This cross-sectional study investigated the association of 5HTTLPR with symptom severity of irritable bowel syndrome (IBS). Patients with IBS (Rome III) and healthy controls were included. Genomic DNA was extracted from saliva, and 5HTTLPR alleles were assessed by polymerase chain reaction. IBS symptom severity was evaluated by means of IBS-SSS questionnaire. Two hundreds and four IBS patients (159 females; mean age: 39.6±12.3 years; 106 with constipation: C-IBS; 98 with diarrhea: D-IBS) and 200 healthy controls (154 females; mean age: 40.4±15.8 years) were enrolled. The overall IBS-SSS value was higher in LS/SS than LL patients (319.0±71.5 versus 283.8±62.3; P = 0.0006). LS/SS patients had also higher values of abdominal pain (59.7±21.0 versus 51.0±18.8; P = 0.020) and bowel dissatisfaction (80.1±23.9 versus 70.5±22.8; P = 0.035). The overall IBS-SSS values in C-IBS and D-IBS patients were 317.2±68.3 and 296.1±71.4, respectively (P = 0.192), with significantly higher values for abdominal distension (65.0±24.4 versus 51.4±24.8; P = 0.0006), but not for bowel dissatisfaction (80.5±21.7 versus 72.9±25.7; P = 0.138). Frequencies of 5HTTLPR genotypes did not differ significantly when comparing IBS patients (overall or upon stratification in C-IBS and D-IBS) with healthy controls. In conclusion, the LS and SS genotypes are significantly correlated with IBS symptom severity, although their possible direct causal role remains to be proven. In addition, the present findings do not support an association of 5HTTLPR with IBS or its clinical presentation in terms of bowel habit predominance.
Citation:Colucci R, Gambaccini D, Ghisu N, Rossi G, Costa F, et al. (2013) Influence of the Serotonin Transporter 5HTTLPR Polymorphism on Symptom Severity in Irritable Bowel Syndrome. PLoS ONE 8(2): e54831. doi:10.1371/journal.pone.0054831
Editor: Yvette Tache, University of California, Los Angeles, United States of America
Received: July 19, 2012; Accepted: December 19, 2012; Published: February 5, 2013
Copyright: © 2013 Colucci et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding:The present work was supported by a grant from the Italian Ministry of Education, University and Research (PRIN 2007, Project number 2007Z292XF_002). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Irritable bowel syndrome (IBS) is a functional digestive disorder characterized by abdominal pain/discomfort and changes in bowel habit (constipation and/or diarrhoea), which can be associated with alterations of gastrointestinal (GI) transit, visceral hypersensitivity and psychopathological comorbidities. ,  Owing to its chronicity and substantial lack of effective cures, IBS results in a significant social burden, with a loss of work productivity, impaired quality of life, and a remarkable use of health care resources. .
From a pathogenic standpoint, IBS is a complex, heterogeneous disorder, whose development is widely considered as multifactorial in nature. ,  Based on current evidence, a gene-environment paradigm has been proposed for IBS, whereby a combination of genetic determinants and environmental factors gives rise to alterations in GI sensation and motor functions, that ultimately account for the occurrence of symptoms. ,  In this context, studies on families or twins have given support to the hypothesis of a genetic background in IBS and, consequently, intensive efforts are being made to evaluate whether specific polymorphisms of a number of candidate genes are pathogenically associated with IBS. ,  Furthermore, since genetic factors do not act necessarily as risk factors, but they can also impact on clinical phenotypes, great attention is being paid also to possible relationships linking genetic polymorphisms to intermediate phenotypes (e.g., GI transit and pain threshold to rectal distension) or clinical presentation/severity. , , .
The involvement of serotonin (5-HT) in the pathophysiology of IBS is also an area of active investigation, owing to its presence in both GI tract and brain. Indeed, 5-HT acts as a main regulator of GI motility, secretion and sensory signalling, and plays also a pivotal role in the control of mood at level of the central nervous system (CNS). ,  The magnitude and duration of 5-HT actions depend mostly on 5-HT transporter (SERT), which mediates the extracellular reuptake of 5-HT, thus ensuring its recycling and catabolic breakdown. ,  Since abnormalities in 5-HT reuptake have the potential of altering the enteric serotonergic signalling, leading to motor, secretory and sensory gut dysfunctions, it has been suggested that genetic or epigenetic SERT variations might contribute to the pathogenesis or clinical presentation of IBS. , .
The promoter region of human SERT gene contains a polymorphism, designated as ‘5-HT transporter length polymorphic region’ (5HTTLPR), which consists of a 44-base pair deletion/insertion, resulting in a short (S) and long (L) allele. ,  The implications of this polymorphism in IBS are currently under evaluation since, as compared with LL genotype, SS or SL genotypes are associated with lower levels of SERT mRNA transcripts, and thereby lower levels of SERT expression and lower efficiency of 5-HT reuptake. , ,  A meta-analysis of association studies has not supported a pathogenic link of 5HTTLPR with IBS.  By contrast, some studies have found a significant association when IBS patients were stratified by their predominant bowel habit,  or were investigated for pain sensation at rectal distension or somatic symptom scores. ,  However, whether 5HTTLPR exerts any influence on symptom severity in IBS remains undetermined. Accordingly, the present study was carried out with the primary purpose of investigating a possible association of 5HTTLPR polymorphism with overall symptom severity in IBS patients.
The primary objective was to examine the association of 5HTTLPR with the overall symptom severity in IBS patients. The secondary objectives were: 1) to evaluate the association of 5HTTLPR with the severity of different symptoms; 2) to evaluate the overall symptom severity and the severity of different IBS symptoms in patients with predominance of constipation (C-IBS) or diarrhoea (D-IBS); 3) to evaluate the association of 5HTTLPR with IBS in all IBS patients, as well as in the subgroups of C-IBS or D-IBS, by comparisons with healthy controls.
Study Design and Population
This study was conducted on native Italians of Caucasian origin, gender of either sex, age equal or higher than 18 years, and diagnosis of IBS according to Rome III criteria,  referred consecutively to the Unit of Gastroenterology from June 2009 to December 2011. Exclusion criteria included: severe organic diseases; history of major abdominal surgery; severe psychiatric disorders; significant alterations of blood chemistry, haematology, and urine analysis; organic lesions at colonoscopy, barium enema, or abdominal ultrasonography; lactose intolerance; treatment with any drug, employed for IBS or affecting the digestive system or CNS, within the previous month. IBS patients with alternation of diarrhea and constipation were also excluded, since changes in the clinical phenotype are common in this subpopulation.  To evaluate the association of 5HTTLPR with IBS, healthy volunteers, consisting of native Italians of Caucasian origin, gender of either sex, and age equal or higher than 18 years, were also enrolled. The exclusion criteria included: body mass index lower than 19 or higher than 25 kg/m2; unremarkable medical history; any functional or organic disease; history of major abdominal surgery; severe psychiatric disorders; food intolerance; any hematologic abnormality.
At least two samples of saliva were collected from each IBS patient and healthy volunteer in different days and stored at −20°C. All subsequent analytical procedures were performed at the Division of Pharmacology and Chemotherapy. The severity of IBS symptoms was evaluated by the questionnaire IBS-Symptom Severity Score (IBS-SSS).  Then all patients received the standard of care. The study protocol was approved by the Ethical Committee of Pisa and was carried out in accordance with the Helsinki Declaration (Edinburgh revision, 2000). A signed informed consent was obtained from each participant.
5HTTLPR Polymorphism Assay
Genomic DNA was isolated from saliva by the alkaline method using QIAamp DNA blood MINI kit (Qiagen, Milano, Italy), quantified by spectrophotometry, and visualized by agarose gel electrophoresis. At the first run, success rates of 97.5% and 95.5% were obtained for DNA extraction in IBS patients and healthy controls, respectively. Additional samples of saliva were then employed or collected again from subjects with extraction failure, and success rates of 100% were achieved at the second run of genomic DNA extraction. In order to avoid and properly manage genotyping errors, for each batch the following cautions were taken as suggested by Pompanon et al. : 1) the laboratory staff was blinded to sample allocation; 2) blanks and duplicate samples of control DNA were included; 3) each sample was assayed in duplicate; 4) cases of genotyping failure in at least one duplicate were resolved by assaying DNA extracted from additional samples of saliva; 5) care was taken to verify whether the genotype distribution was in Hardy-Weinberg equilibrium. The 5HTTLPR polymorphism was typed by polymerase chain reaction (PCR) using the following oligonucleotide primers: forward (LPR-F), 5′-GGCGTTGCCGCTCTGAATGC-3′, spanning from nucleotide –1416 to –1397; reverse (LPR-R), 5′-GAGGGACTGAGCTGGACAACCAC-3′, spanning from –910 to –888. PCR was performed with the GC-Rich PCR system (Roche Molecular Biochemicals), in a 50-µl reaction containing 1 µl of genomic DNA (20–50 ng), 25 µl of DNAase free H2O, 1 µl of 10 mM dNTP, 1 µl of 10 mM LPR-F primer, 1 µl of 10 mM LPR-R primer, 10 µl of BUFFER GC resolution, 10 µl of BUFFER 5× DMSO and 1 µl of AmpliTaq polymerase enzyme (ROCHE Diagnostics, Milano, Italy). DNA was denatured at 94°C for 3 min and subjected to 35 cycles of 1 min of denaturation at 94°C, 1 min of annealing at 55°C, 1 min of extension at 72°C, and 7 min of final extension at 72°C. Amplification products were resolved by electrophoresis on 2% agarose gel, and visualized with ethidium bromide staining. The image was acquired by means of a Kodak Image Station 440. The alleles containing the S or L variant of 5HTTLPR yielded PCR products of 528 and 572 base pairs, respectively. Based on PCR results, the enrolled subjects were classified as having the LL, LS or SS genotype.
Evaluation of Symptom Severity
The IBS-SSS questionnaire takes into account the following items: a) presence and severity of abdominal pain or discomfort; b) frequency of abdominal pain or discomfort; c) presence and severity of abdominal distension; d) degree of satisfaction of defecatory behaviour; e) degree of interference of IBS symptoms with daily lifestyle. Each of the above items generates a maximum score of 100, leading to an overall score of 500. .
Primary endpoint: overall IBS-SSS value, to compare LL versus LS/SS genotypes in patients. Secondary endpoints: 1) value of each IBS-SSS item, to compare LL versus LS/SS genotypes in patients; 2) overall IBS-SSS value, to compare C-IBS versus D-IBS patients; 3) value of each IBS-SSS item, to compare C-IBS versus D-IBS patients; 4) frequencies of LL and LS/SS genotypes, to compare IBS patients with healthy volunteers; 5) frequencies of LL and LS/SS genotypes, to compare C-IBS patients, D-IBS patients and healthy volunteers.
Data were expressed as mean ± standard deviation (SD) for continuous variables, and as percentage for qualitative variables. Comparisons between groups were performed by analysis of variance (ANOVA) and the non-parametric Wilcoxon unpaired test for continuous variables, and by the Pearson’s chi-square or the Fisher’s exact test for categorical variables. Adjustments for multiple comparisons were carried out by the Bonferroni correction. Comparisons between groups for IBS-SSS values were also performed by a two-factor (genotype and IBS subgroups) ANOVA, and the two-factor interaction was evaluated. The patients sample size was determined to evaluate a between-groups (LL versus LS/SS genotype) difference of 30 in the mean overall IBS-SSS value, with a standard deviation of 65, a first type error of 0.05 and a power of 0.80. A 2-sided P value <0.05 was considered to be statistically significant. Statistical analysis was performed by JMP 4.0 (SAS Institute Inc., Cary, NC, U.S.A.) and StatXact-4 (Cytel Software Corporation, Cambridge, MA, U.S.A.).
Influence of 5HTTLPR Genotypes on IBS Symptom Severity
Two hundreds and four consecutive patients (45 males, 159 females; mean age: 39.6±12.3 years), with a diagnosis of C-IBS (6 males, 100 females; mean age: 41.2±12.9 years) or D-IBS (39 males, 59 females; mean age: 38.0±11.5 years), were enrolled to assess the relationship between 5HTTLPR genotypes and IBS symptom severity. The C-IBS and D-IBS subgroups differed significantly for male/female proportion (P<0.0001), but not for age. For the purpose of analyzing the primary and secondary endpoints, the subjects with SS and LS genotypes were pooled (LS/SS), since the S allele has been reported to be dominant and both SS and LS genotypes have been associated with a lower SERT expression and reduced efficiency of 5-HT uptake, as compared with the LL genotype. ,  However, in order to perform additional exploratory evaluations, subjects with genotypes LS and SS were also analysed as separate groups.
The overall mean symptom severity, as assessed by IBS-SSS, was significantly higher in patients with LS/SS than LL genotype (Table 1). When comparing the mean values obtained for each IBS-SSS item, ‘abdominal pain severity’ and ‘bowel dissatisfaction’ were significantly higher in patients with LS/SS than LL genotype, while no significant differences were found with regard for the ‘occurrence of pain over the preceding 10 days’, ‘abdominal distension severity’, and ‘interference with quality of life’ (Table 1). These findings were confirmed also when the P values were adjusted for multiple comparisons by the Bonferroni correction. Of note, an exploratory analysis showed that, when comparing patients with LS and SS genotypes as separate groups, there were no significant differences with regard for the overall symptom severity (P = 0.496) and single-item IBS-SSS values (abdominal pain severity, P = 0.935; occurrence of pain over the preceding ten days, P = 0.348; abdominal distension severity, P = 0.968; bowel dissatisfaction, P = 0.309; interference with quality of life, P = 0.851).
Symptom severity was assessed also in C-IBS and D-IBS patients. The overall mean IBS-SSS values were found to be significantly higher in the C-IBS than D-IBS subgroup, irrespectively of their 5HTTLPR genotype (Table 2). Likewise, when evaluating symptom severity by single items, the score values for ‘abdominal distension severity’ and ‘bowel dissatisfaction’ were significantly higher in C-IBS than D-IBS patients (Table 2). However, upon application of Bonferroni correction, the significance of differences in terms of overall symptom severity and bowel dissatisfaction were lost (P = 0.192 and 0.138, respectively), while the significance of differences concerning abdominal distension severity was confirmed (P = 0.0006).
There was a lack of significant interaction between bowel habits (i.e., C-IBS and D-IBS) and 5HTTLPR genotypes, indicating no effect modification and independent effects of bowel habits and genotypes on symptom severity (interaction P values: 0.297 for overall IBS-SSS value; 0.078 for abdominal pain severity; 0.481 for occurrence of pain over the preceding 10 days; 0.811 for abdominal distension severity; 0.379 for bowel dissatisfaction; 0.406 for interference with quality of life).
Association of 5HTTLPR Polymorphism with IBS
In order to evaluate whether 5HTTLPR polymorphism is associated with IBS in the present group of patients, a comparison was made with a group of healthy controls. For this purpose, 200 healthy volunteers (46 males, 154 females; mean age: 40.4±15.8 years) were enrolled in the study. They did not differ significantly in terms of male/female proportion and mean age from the group of IBS patients.
The frequencies of 5HTTLPR genotypes in IBS patients and healthy volunteers are displayed in Table 3. Care was taken to verify that the genotype distribution in healthy volunteers was in Hardy-Weinberg equilibrium (chi-square = 0.21, P = 0.646). In order to allow comparisons with previous observations, the LS and SS genotypes were analyzed either separately or as a pooled group (LS/SS). In both cases, the frequencies of LL, LS, SS or LS/SS genotypes in IBS patients did not differ significantly from those estimated in healthy volunteers (Table 3). Likewise, genotypes frequencies did not differ significantly when the comparisons were conducted on IBS patients after their stratification into two subgroups, according to the predominance of constipation or diarrhea (Table 4).
Great attention is currently revolving around the pathogenic bases and pathophysiological mechanisms accounting for the clinical manifestations of IBS, ,  and there is consistent evidence suggesting an influence of genetic factors on this disorder. ,  In this context, our study provides the first evidence that 5HTTLPR impacts on the severity of IBS symptoms. In particular, our findings point out a higher degree of symptom severity in patients with at least one S allele, and suggest that the S variant affects mainly the severity of abdominal pain and bowel dissatisfaction. Of note, our exploratory analysis showed that IBS-SSS values did not differ significantly when comparing subgroups with LS and SS genotypes, thus suggesting that the group of patients with pooled LS/SS genotypes was a homogeneous population.
The contention that the LS/SS genotypes can increase the severity of IBS symptoms, with particular regard for abdominal pain, is supported by previous investigations. In particular our findings are in line with data from Camilleri et al.  who found that the LS/SS genotypes are associated with increased pain sensation at rectal distension. Taken together, these observations  and our results are consistent with the notion that the S allele is expected to impair the efficiency of 5-HT reuptake with a consequent prolonged and enhanced activation of serotonergic pathways mediating abdominal pain sensation. Therefore, it can be argued that the reduced 5-HT re-uptake could induce an overstimulation of extrinsic nerve afferents resulting in neuronal sensory sensitisation, which might occur at peripheral, spinal, or even higher CNS levels. ,  In this regard, an interesting study by Fukudo et al. , aimed at evaluating the link between 5HTTLPR and differential activation of brain regions by colorectal distention in humans, displayed that individuals with a weak function of serotonin transporter (i.e. S/S genotype) responded to signals from gut with higher intensity in emotion-regulating brain regions, thus suggesting that this functional gene polymorphism may partly predict the individual effects of selective serotonin reuptake inhibitors on visceral pain. .
Whether the influence of 5HTTLPR on abdominal pain results mainly from peripheral or central mechanisms, or both, is presently unknown and remains open to future investigations. However, some evidence suggests that central mechanisms may contribute to the enhanced pain perception in IBS patients with LS/SS genotypes: 1) specific brain regions of IBS patients and healthy controls are subjected to differential activation upon application of rectal stimuli;  2) brain regions highly related to pain recognition and emotion (e.g. anterior cingulated cortex) were found to be more activated by distension of descending colon in IBS patients,  and altered interactions between anterior cingulated cortex and amygdala have been reported in subjects with LS/SS genotypes;  3) individuals with the SS genotype were more likely to activate these CNS regions, thus suggesting that the S variant can be relevant in brain activation after colorectal distension in IBS patients.  Further support to the contribution of central nervous mechanisms on the association of 5HTTLPR with symptom severity in IBS comes from the observations that: 1) in IBS patients, the LS/SS genotypes were associated with high values of somatic symptom scores, suggesting that 5-HTTLPR is implicated in the responses of IBS patients to stress;  2) individuals with the S allele display higher vulnerability to stressful life events and are more prone to develop depressive symptoms. . In this respect, to assess whether the influence of S allele on abdominal pain severity, could be related to differences in patients’ psychopathological traits would be of high interest, and this issue deserves future investigations.
In the present study, when the P values were adjusted for multiple comparisons, the analysis for secondary endpoints revealed that the overall symptom severity did not differ in C- and D-IBS patients, while the analysis of single severity items displayed significant differences only for the severity of abdominal distension. Moreover, our analysis showed a lack of significant interaction between bowel habits and 5HTTLPR genotypes. These findings were not completely unexpected, since C-IBS patients are known to complain of abdominal distension more than D-IBS patients.  In addition, and most importantly, these data argue against the possibility that the differential influences of 5HTTLPR genotypes on abdominal pain severity might result from differences in bowel habit.
The influence of 5HTTLPR on IBS symptom severity and, particularly, on abdominal pain severity, might have interesting implications for the effectiveness and/or safety of drugs proposed for the therapeutic management of this syndrome. SERT is a specific target of ‘selective serotonin reuptake inhibitors’ (SSRIs) and there is evidence linking 5HTTLPR to the efficacy and safety of these drugs in patients with depression. ,  It is being also appreciated that SSRIs can exert beneficial effects on IBS, with particular regard for the control of abdominal discomfort or pain, ,  but whether SERT polymorphisms may influence such therapeutic responses remains unknown.
To date, most of the studies on the impact of 5-HT genetics on IBS have investigated the associations of 5HTTLPR with its pathogenesis or clinical presentation. In this regard, the present study was conducted also with the secondary objective of evaluating whether any of such associations could be highlighted in our IBS patients. For this purpose, the frequencies of their 5HTTLPR genotypes were compared with those of healthy controls, selected with similar demographic characteristics, and no significant association was found either for the overall IBS group or for the subgroups of C-IBS and D-IBS patients. Our results are consistent with the majority of previous studies ,  which failed in finding a link between 5HTTLPR and IBS. Moreover, while most authors did not find specific links of 5HTTLPR with C-IBS or D-IBS, , , , ,  others have reported significant associations of SS with D-IBS, ,  SS with C-IBS,  or LL with C-IBS. , ,  Among the variety of factors which might account for the heterogeneity of these observations, the most relevant relies perhaps in the different distribution of 5HTTLPR genotypes among different populations. In particular, the allele frequencies between Caucasian and Asian populations are different, since S allele is found in 42% of Caucasians and in 79% of Asians.  Furthermore, significant variations in the frequency of 5HTTLPR genotypes can be found even in populations sharing the same Caucasian origin, but belonging to distinct ethnicities.  In this respect, both the IBS patients and healthy volunteers evaluated in our study were highly homogeneous, as we enrolled only white Caucasian subjects of Italian origin.
In conclusion, the present study suggests that the LS and SS genotypes are significantly correlated with IBS symptom severity, although their possible direct causal role remains to be proven. In addition, the present findings do not support an association of 5HTTLPR with IBS or its clinical presentation in terms of bowel habit predominance.
Conceived and designed the experiments: CB MB RC SM NDB. Performed the experiments: RC NG GR. Analyzed the data: RC DG AR MGM NG MF LA MT. Contributed reagents/materials/analysis tools: NG MGM DG. Wrote the paper: MB CB SM FC GR.
- 1. Longstreth GF, Thompson WG, Chey WD, Houghton LA, Mearin F, et al. (2006) Functional bowel disorders. Gastroenterology 130: 1480–1491. doi: 10.1053/j.gastro.2005.11.061
- 2. Brandt LJ, Chey WD, Foxx-Orenstein AE, Schiller LR, Schoenfeld PS, et al. (2009) An evidence-based position statement on the management of irritable bowel syndrome. Am J Gastroenterol 104 Suppl 1S1–35.
- 3. Spiller R (2007) Clinical update: irritable bowel syndrome. Lancet 369: 1586–1588. doi: 10.1016/s0140-6736(07)60726-0
- 4. Ohman L, Simren M (2007) New insights into the pathogenesis and pathophysiology of irritable bowel syndrome. Dig Liver Dis 39: 201–215. doi: 10.1016/j.dld.2006.10.014
- 5. Hasler WL (2011) Traditional thoughts on the pathophysiology of irritable bowel syndrome. Gastroenterol Clin North Am 40: 21–43. doi: 10.1016/j.gtc.2010.12.004
- 6. Saito YA (2011) The role of genetics in IBS. Gastroenterol Clin North Am 40: 45–67. doi: 10.1016/j.gtc.2010.12.011
- 7. Camilleri M, Katzka DA (2012) Genetic epidemiology and pharmacogenetics in irritable bowel syndrome. Am J Physiol Gastrointest Liver Physiol 302: G1075–1084. doi: 10.1152/ajpgi.00537.2011
- 8. Adam B, Liebregts T, Holtmann G (2007) Mechanisms of disease: genetics of functional gastrointestinal disorders–searching the genes that matter. Nat Clin Pract Gastroenterol Hepatol 4: 102–110. doi: 10.1038/ncpgasthep0717
- 9. Hamaguchi T, Kano M, Rikimaru H, Kanazawa M, Itoh M, et al. (2004) Brain activity during distention of the descending colon in humans. Neurogastroenterol Motil 16: 299–309. doi: 10.1111/j.1365-2982.2004.00498.x
- 10. Camilleri M, Busciglio I, Carlson P, McKinzie S, Burton D, et al. (2008) Candidate genes and sensory functions in health and irritable bowel syndrome. Am J Physiol Gastrointest Liver Physiol 295: G219–225. doi: 10.1152/ajpgi.90202.2008
- 11. Fukudo S, Kanazawa M, Mizuno T, Hamaguchi T, Kano M, et al. (2009) Impact of serotonin transporter gene polymorphism on brain activation by colorectal distention. Neuroimage 47: 946–951. doi: 10.1016/j.neuroimage.2009.04.083
- 12. Kim DY, Camilleri M (2000) Serotonin: a mediator of the brain-gut connection. Am J Gastroenterol 95: 2698–2709.
- 13. Gershon MD (2005) Nerves, reflexes, and the enteric nervous system: pathogenesis of the irritable bowel syndrome. J Clin Gastroenterol 39: S184–193. doi: 10.1097/01.mcg.0000156403.37240.30
- 14. Chen JX, Pan H, Rothman TP, Wade PR, Gershon MD (1998) Guinea pig 5-HT transporter: cloning, expression, distribution, and function in intestinal sensory reception. Am J Physiol 275: G433–448.
- 15. Mawe GM, Coates MD, Moses PL (2006) Review article: intestinal serotonin signalling in irritable bowel syndrome. Aliment Pharmacol Ther 23: 1067–1076. doi: 10.1111/j.1365-2036.2006.02858.x
- 16. Colucci R, Blandizzi C, Bellini M, Ghisu N, Tonini M, et al. (2008) The genetics of the serotonin transporter and irritable bowel syndrome. Trends Mol Med 14: 295–304. doi: 10.1016/j.molmed.2008.05.001
- 17. Heils A, Teufel A, Petri S, Stober G, Riederer P, et al. (1996) Allelic variation of human serotonin transporter gene expression. J Neurochem 66: 2621–2624. doi: 10.1046/j.1471-4159.1996.66062621.x
- 18. Lesch KP (2001) Variation of serotonergic gene expression: neurodevelopment and the complexity of response to psychopharmacologic drugs. Eur Neuropsychopharmacol 11: 457–474. doi: 10.1016/s0924-977x(01)00123-7
- 19. Lesch KP, Bengel D, Heils A, Sabol SZ, Greenberg BD, et al. (1996) Association of anxiety-related traits with a polymorphism in the serotonin transporter gene regulatory region. Science 274: 1527–1531. doi: 10.1126/science.274.5292.1527
- 20. Hranilovic D, Stefulj J, Schwab S, Borrmann-Hassenbach M, Albus M, et al. (2004) Serotonin transporter promoter and intron 2 polymorphisms: relationship between allelic variants and gene expression. Biol Psychiatry 55: 1090–1094. doi: 10.1016/j.biopsych.2004.01.029
- 21. Wang YM, Chang Y, Chang YY, Cheng J, Li J, et al. (2012) Serotonin transporter gene promoter region polymorphisms and serotonin transporter expression in the colonic mucosa of irritable bowel syndrome patients. Neurogastroenterol Motil 24: 560–e255. doi: 10.1111/j.1365-2982.2012.01902.x
- 22. Van Kerkhoven LA, Laheij RJ, Jansen JB (2007) Meta-analysis: a functional polymorphism in the gene encoding for activity of the serotonin transporter protein is not associated with the irritable bowel syndrome. Aliment Pharmacol Ther 26: 979–986. doi: 10.1111/j.1365-2036.2007.03453.x
- 23. Yeo A, Boyd P, Lumsden S, Saunders T, Handley A, et al. (2004) Association between a functional polymorphism in the serotonin transporter gene and diarrhoea predominant irritable bowel syndrome in women. Gut 53: 1452–1458. doi: 10.1136/gut.2003.035451
- 24. Kim HJ, Camilleri M, Carlson PJ, Cremonini F, Ferber I, et al. (2004) Association of distinct alpha(2) adrenoceptor and serotonin transporter polymorphisms with constipation and somatic symptoms in functional gastrointestinal disorders. Gut 53: 829–837. doi: 10.1136/gut.2003.030882
- 25. Garrigues V, Mearin F, Badia X, Balboa A, Benavent J, et al. (2007) Change over time of bowel habit in irritable bowel syndrome: a prospective, observational, 1-year follow-up study (RITMO study). Aliment Pharmacol Ther 25: 323–332. doi: 10.1111/j.1365-2036.2006.03197.x
- 26. Francis CY, Morris J, Whorwell PJ (1997) The irritable bowel severity scoring system: a simple method of monitoring irritable bowel syndrome and its progress. Aliment Pharmacol Ther 11: 395–402. doi: 10.1046/j.1365-2036.1997.142318000.x
- 27. Pompanon F, Bonin A, Bellemain E, Taberlet P (2005) Genotyping errors: causes, consequences and solutions. Nature Rev Genet 6: 847–59. doi: 10.1038/nrg1707
- 28. Mayer EA, Gebhart GF (1994) Basic and clinical aspects of visceral hyperalgesia. Gastroenterology 107: 271–293.
- 29. Fukudo S, Kanazawa M, Mizuno T, Hamaguchi T, Kano M, et al. (2009) Impact of serotonin transporter gene polymorphism on brain activation by colorectal distention. Neuroimage 47: 946–951. doi: 10.1016/j.neuroimage.2009.04.083
- 30. Mertz H, Morgan V, Tanner G, Pickens D, Price R, et al. (2000) Regional cerebral activation in irritable bowel syndrome and control subjects with painful and nonpainful rectal distention. Gastroenterology 118: 842–848. doi: 10.1016/s0016-5085(00)70170-3
- 31. Pezawas L, Meyer-Lindenberg A, Drabant EM, Verchinski BA, Munoz KE, et al. (2005) 5-HTTLPR polymorphism impacts human cingulate-amygdala interactions: a genetic susceptibility mechanism for depression. Nat Neurosci 8: 828–834. doi: 10.1038/nn1463
- 32. Caspi A, Sugden K, Moffitt TE, Taylor A, Craig IW, et al. (2003) Influence of life stress on depression: moderation by a polymorphism in the 5-HTT gene. Science 301: 386–389. doi: 10.1126/science.1083968
- 33. Gerson CD, Gerson MJ, Awad RA, Chowdhury A, Dancey C, et al. (2008) Irritable bowel syndrome: an international study of symptoms in eight countries. Eur J Gastroenterol Hepatol 20: 659–667. doi: 10.1097/meg.0b013e3282f53a24
- 34. Smits KM, Smits LJ, Schouten JS, Stelma FF, Nelemans P, et al. (2004) Influence of SERTPR and STin2 in the serotonin transporter gene on the effect of selective serotonin reuptake inhibitors in depression: a systematic review. Mol Psychiatry 9: 433–441. doi: 10.1038/sj.mp.4001488
- 35. Serretti A, Calati R, Mandelli L, De Ronchi D (2006) Serotonin transporter gene variants and behavior: a comprehensive review. Curr Drug Targets 7: 1659–1669. doi: 10.2174/138945006779025419
- 36. Ford AC, Talley NJ, Schoenfeld PS, Quigley EM, Moayyedi P (2009) Efficacy of antidepressants and psychological therapies in irritable bowel syndrome: systematic review and meta-analysis. Gut 58: 367–378. doi: 10.1136/gut.2008.163162
- 37. Lee DY, Park H, Kim WH, Lee SI, Seo YJ, et al. (2004) [Serotonin transporter gene polymorphism in healthy adults and patients with irritable bowel syndrome]. Korean J Gastroenterol 43: 18–22.
- 38. Saito YA, Locke GR, 3rd, Zimmerman JM, Holtmann G, Slusser JP, et al (2007) A genetic association study of 5-HTT LPR and GNbeta3 C825T polymorphisms with irritable bowel syndrome. Neurogastroenterol Motil 19: 465–470. doi: 10.1111/j.1365-2982.2007.00905.x
- 39. Kohen R, Jarrett ME, Cain KC, Jun SE, Navaja GP, et al. (2009) The serotonin transporter polymorphism rs25531 is associated with irritable bowel syndrome. Dig Dis Sci 54: 2663–2670. doi: 10.1007/s10620-008-0666-3
- 40. Niesler B, Kapeller J, Fell C, Atkinson W, Moller D, et al. (2010) 5-HTTLPR and STin2 polymorphisms in the serotonin transporter gene and irritable bowel syndrome: effect of bowel habit and sex. Eur J Gastroenterol Hepatol 22: 856–861. doi: 10.1097/meg.0b013e32832e9d6b
- 41. Park JM, Choi MG, Park JA, Oh JH, Cho YK, et al. (2006) Serotonin transporter gene polymorphism and irritable bowel syndrome. Neurogastroenterol Motil 18: 995–1000. doi: 10.1111/j.1365-2982.2006.00829.x
- 42. Sikander A, Rana SV, Sinha SK, Prasad KK, Arora SK, et al. (2009) Serotonin transporter promoter variant: Analysis in Indian IBS patients and control population. J Clin Gastroenterol 43: 957–961. doi: 10.1097/mcg.0b013e3181b37e8c
- 43. Li Y, Nie Y, Xie J, Tang W, Liang P, et al. (2007) The association of serotonin transporter genetic polymorphisms and irritable bowel syndrome and its influence on tegaserod treatment in Chinese patients. Dig Dis Sci 52: 2942–2949. doi: 10.1007/s10620-006-9679-y
- 44. Noskova T, Pivac N, Nedic G, Kazantseva A, Gaysina D, et al. (2008) Ethnic differences in the serotonin transporter polymorphism (5-HTTLPR) in several European populations. Prog Neuropsychopharmacol Biol Psychiatry 32: 1735–1739. doi: 10.1016/j.pnpbp.2008.07.012