Literature DB >> 28814899

Irritable bowel symptoms and the development of common mental disorders and functional somatic syndromes identified in secondary care - a long-term, population-based study.

Chalotte Heinsvig Poulsen1,2, Lene Falgaard Eplov2, Carsten Hjorthøj2, Marie Eliasen1, Sine Skovbjerg1, Thomas Meinertz Dantoft1, Andreas Schröder3, Torben Jørgensen1,4,5.   

Abstract

OBJECTIVE: Irritable bowel syndrome (IBS) is associated with mental vulnerability, and half of patients report comorbid somatic and mental symptoms. We aimed to investigate the relationship between an IBS symptom continuum and the subsequent development of common mental disorders (CMDs) and functional somatic syndromes (FSSs). METHODS AND STUDY
DESIGN: A longitudinal population-based study comprising two 5-year follow-up studies, Dan-MONICA 1 (1982-1987) and Inter99 (1999-2004), recruited from the western part of Copenhagen County. The total study population (n = 7,278) was divided into symptom groups according to the degree of IBS definition fulfillment at baseline and/or follow-up and was followed until December 2013 in Danish central registries. Cox regression was used for the analyses, adjusting for age, sex, length of education and cohort membership. In a subsequent analysis, we adjusted for mental vulnerability as a risk factor for both CMDs and FSSs, including IBS.
RESULTS: Over a 5-year period, 51% patients had no IBS symptoms, 17% patients had IBS symptoms without abdominal pain, 22% patients had IBS symptoms including abdominal pain and 10% patients fulfilled the IBS definition. IBS and IBS symptoms including abdominal pain were significantly associated with the development of CMDs and other FSSs identified in secondary care. When adjusting for mental vulnerability, IBS and IBS symptoms including abdominal pain were no longer associated with CMDs, but the significant relationship to other FSSs remained.
CONCLUSION: In a clinical setting, the perspective should be broadened to individuals not fulfilling the symptom cluster of IBS but who report frequent abdominal pain. Additionally, it is important to combine symptom-based criteria of IBS with psychosocial markers such as mental vulnerability, because it could guide clinicians in decisions regarding prognosis and treatment.

Entities:  

Keywords:  abdominal pain; comorbidity; functional gastrointestinal symptoms; neuroticism; somatization

Year:  2017        PMID: 28814899      PMCID: PMC5546191          DOI: 10.2147/CLEP.S141344

Source DB:  PubMed          Journal:  Clin Epidemiol        ISSN: 1179-1349            Impact factor:   4.790


Introduction

With a prevalence of ~11–16%,1,2 “irritable bowel syndrome” (IBS) is a common functional gastrointestinal disorder that is associated with substantial costs for patients, health care systems and society.3 Approximately half of IBS patients report additional mental and somatic symptoms.4 In a Norwegian population-based study, the presence of comorbid symptoms beyond IBS symptoms was associated with a higher functional impairment, more psychological distress and increased health care use.5 Thus, IBS patients have an increased prevalence of mental disorders, especially anxiety and depression.6 Moreover, IBS has a significant symptom overlap with other functional gastrointestinal disorders such as dyspepsia and functional somatic syndromes (FSSs), eg, fibromyalgia and chronic fatigue syndrome.4,7 These findings illustrate the need for more knowledge about the prognosis of IBS, eg, the potential development of mental and functional comorbidities. This knowledge could guide clinicians and policy makers in decisions regarding treatment, disease prevention and health-promoting strategies. Most of the literature in this field has certain methodological limitations such as cross-sectional design, selected patient populations and uncertainties in delimitation of the FSSs including IBS.4,6,7 Recently, IBS has been defined as a disorder of gut–brain interaction;8 that is why studies focusing on IBS and subsequent development of mental and functional comorbidities have become of increasing interest.9–12 Never theless, the focus is on IBS and “non-IBS” cases, although other population-based studies have shown the importance of broadening the perspective to individuals not fulfilling the symptom cluster of IBS.2,13,14 Additionally, other population-based studies have shown that mental vulnerability, illness anxiety and somatic symptom burden predict development of IBS.15,16 These results indicate the need for addressing both somatic and psychological factors in the early examination of individuals with IBS. Mental vulnerability represents both a symptom state related to somatization and a personality trait related to neuroticism.17 Neuroticism has been shown to be a risk marker in the development of common mental disorders (CMDs).18 In addition, both neuroticism and somatization have been linked to the development of IBS and other FSSs.19,20 Therefore, long-term population-based studies taking psychosocial factors such as mental vulnerability into account are warranted. In the present study, we hypothesized that mental and functional comorbidities also are present among individuals not fulfilling the IBS definition. We therefore broadened the perspective to a continuum of IBS symptoms in a general population. Furthermore, we combined cohort studies with Danish nationwide registers and aimed to investigate the association between IBS symptoms and the subsequent development of CMDs and FSSs other than IBS. Additionally, we hypothesized that mental vulnerability can act as a confounder, because it may contribute to both predisposition and maintenance of IBS symptoms.19 We therefore aimed to investigate these associations both with and without taking mental vulnerability into account.

Methods and study design

The study design has previously been presented as a longitudinal study consisting of two population-based cohorts, Dan-MONICA 1 (1982–1987) and Inter99 (1999–2004), both examined twice with 5-year interval.14 The two cohorts were followed until December 2013 in Danish central registries.

Study populations

The two study populations have previously been described in detail.21,22 They were drawn as age- and sex-matched samples from the Danish Civil Registration System (CRS) using computer-generated random numbers. Both study populations were recruited from the western part of Copenhagen County, which constitutes 7% of the total Danish population and is representative of Danes living in the suburbs. In brief, the Dan-MONICA 1 study population comprised 4,807 men and women of ages 30, 40, 50 and 60 years.21 All individuals were invited for a general health examination conducted in 1982–1984. Individuals not of Danish nationality (n = 226) were excluded, reducing the sample to 4,581. Of them, 3,608 (79%) individuals participated in the baseline study. At the 5-year follow-up, 3,498 individuals were accessible for invitation to a similar health examination. Among them, 2,987 (85%) individuals participated. Individuals not responding were re-invited twice.23 The Inter99 study population comprised 13,016 men and women of ages 30, 35, 40, 45, 50, 55 and 60 years.22 Eligible individuals (n = 12,934) were invited for a health screening program conducted in 1999–2001, and 6,906 (53%) individuals turned up for the examination. Individuals with linguistic barriers, alcoholism or drug abuse were excluded, leaving 6,784 (52.5%) participants in the baseline study. The Inter99 study was designed as an intervention study for prevention of ischemic heart disease. The participants were therefore divided into two random samples: a high-intensity intervention group (A) and a low-intensity intervention group (B). At the 5-year follow-up, 6,536 individuals were accessible for invitation to the second study. Among them, 4,513 (69%) individuals participated. Individuals not responding were re-invited.24 Both cohorts comprised information on self-reported IBS symptoms from a questionnaire and were pooled in the present study, reducing the sample to 7,500 individuals who participated both at baseline and at 5-year follow-up. The data from Dan-MONICA 1 and Inter99 are available for researchers who meet the criteria, for access to confidential data contact information: torben.joergensen@regionh.dk.

IBS symptom groups

The used IBS definition was based on a symptom cluster of frequent self-reported IBS symptoms in the past 12 months found in a previous study of Dan-MONICA 1: “Individuals stating that they often experience both abdominal pain and distension and, additionally, either borborygmus or altering stool consistency, or both”.25 Frequent IBS symptoms were defined as experiencing them at least once a month (abdominal pain) or frequently or daily/almost constantly (distension, borborymus and altering stool consistency). The total study population was divided into four symptom groups according to the degree of IBS definition fulfillment at baseline and/or 5 years follow-up: 1) IBS; 2) IBS symptoms including abdominal pain; 3) IBS symptoms without abdominal pain and 4) reference group without IBS symptoms. Individuals in group 1 fulfilled the IBS definition at baseline and/or 5-year follow-up. Individuals in group 2 and 3 had IBS symptoms with and without abdominal pain at baseline and/or at 5-year follow-up but did not fulfill the IBS definition at any time. The reference group had no IBS symptoms at baseline or at 5-year follow-up. The symptom groups have previously been presented. The study showed that fulfillment of the used IBS definition delimitated individuals not associated with severe gastrointestinal diseases including inflammatory bowel disorders.14 In total, 222 individuals were excluded from the study population due to missing data on IBS symptoms, reducing the sample to 7,278 individuals.

Outcomes

The total study population was linked through the unique personal identification number to the CRS, the Danish Psychiatric Central Research Register (PCRR) and the National Patient Register (NPR). The personal identification number is used in all the registries, insuring complete linkage between databases. The information in the CRS is considered to be of high validity.26 Although both the content and the definitions of single variables may have changed over time, the PCRR and the NPR are considered as valuable tools in epidemiological research.27,28 In this study, we obtained information on psychiatric and somatic inpatient admissions from the PCRR since 1969 and the NPR since 1977 until the end of register extraction (December 31, 2013). From 1995 and onward, the registers also included information of outpatient treatment and emergency room contacts. We based the delimitation of CMDs and other FSSs on systematic reviews and recent register-based studies on the most common mental and functional comorbidities in IBS.4,6,7,10,29 Thus, CMDs were defined as first hospital contact with a diagnosis of a neurotic, stress-related, anxiety or mood affective disorder classified according to the International Classification of Diseases revision 8 (ICD-8) and International Classification of Diseases revision 10 (ICD-10; Table 1). Hypochondriasis was included as an anxiety disorder, because both scientific evidence and clinical evidence support the view that it is a distinct “health anxiety” disorder that can be treated effectively and only partly overlaps with FSSs.30 Other FSSs were defined as first hospital contact for a diagnosis of interstitial cystitis, postviral fatigue syndrome, malaise and fatigue, myalgia/rheumatism unspecified, fibromyalgia, pain not elsewhere classified, temporomandibular joint disorders, sprain and strain of cervical spine (whiplash), somatoform disorders and neurasthenia classified according to ICD-8 and ICD-10 (Table 1).4,6,7,10 In the delimitation, we included unspecific symptom codes due to uncertainties in the registration practice of the syndrome codes.10 We did not include functional gastrointestinal disorders due to the significant symptom overlap with IBS.31,32
Table 1

Definitions of CMDs and FSSs according to ICD-8 and ICD-10

ClassificationCodesClassificationCodes

ICD-8 (1965)ICD-10 (1990)
Neurotic, stress-related and anxiety disorders
Phobic neurosis300.29Phobic anxiety disordersF40
Anxiety/hysterical neurosis300.09–300.19Other anxiety disordersF41
Obsessive–compulsive neurosis300.39Obsessive–compulsive disorderF42
Reaction to severe stress and adjustment disordersF43
Depersonalization syndrome300.69Dissociative (conversion) disordersF44
Hypochondriacal neurosis and other300.79–300.99Hypochondriacal disorderF45.2
Mood affective disorders
Manic-depression psychosis, manic/circular type296.19+296.39Manic episode and bipolar disordersF30–F31
Affective psychoses, depressed type296.09+296.29+ 296.89+296.99+ 300.49Depressive episode and recurrent depressive disordersF32–F33
Other mood affective disordersF34–F39
Functional somatic syndromes
Interstitial cystitis (chronic)N30.1
Postviral fatigue syndromeG93.3
Malaise and fatigueR53
Other muscular rheumatism, fibrositis and myalgia717.99Myalgia/rheumatism unspecifiedM79.0–M79.1
FibromyalgiaM79.7
Pain – not elsewhere classifiedR52
Temporomandibular joint disordersK.07.6
Sprain and strain of other and unspecified parts of backN847Sprain and strain of cervical spine (whiplash)S13.4
Physical disorders, presumably of psychogenic origin305Somatoform disordersF45–F45.1+F45.3–F45.9
Neurasthenia300.59NeurastheniaF48.0

Abbreviations: CMDs, common mental disorders; FSSs, functional somatic syndromes; ICD-8, International Classification of Diseases revision 8; ICD-10, International Classification of Diseases revision 10.

Covariates

Age at health examination and sex were obtained from the CRS. Education was self-reported and obtained from the questionnaires used at the health examinations.21,22 Length of education was categorized as no/under education, <2 years of education (short education, special workers or apprentices), 2–4 years of education (middle length education or technician training) and >4 years of education (academic or higher education). Only eight individuals were under education, and they were categorized as individuals not having an education. The Mental Vulnerability Questionnaire was developed by the Military Psychological Services in Denmark in the 1960s and used as a screening instrument to assess mental fitness for military service. The questionnaire was similar to international instruments developed in the same period.33,34 We used the 12-item Mental Vulnerability Scale (Table S1) that was developed from a 22-item scale derived from the original 27-item Mental Vulnerability Questionnaire.35 The 12-item Mental Vulnerability Scale has been shown to be a predictor of several health outcomes, including IBS, upper dyspepsia and depression.15,36–38 Moreover, the 12-item scale has been validated as a reliable and stable measure of overall mental vulnerability.17 Mental vulnerability was categorized as not vulnerable (zero to two affirmative answers), moderately vulnerable (three to four affirmative answers) and highly vulnerable (five or more affirmative answers).

Statistical analysis

We analyzed data using SAS 9.3 software (SAS Institute Inc., Cary, NC, USA). The associations between each of the symptom groups, CMDs and FSSs were assessed using Cox proportional hazards regression models to estimate hazard ratios (HRs) with 95% confidence intervals (CIs). Follow-up time was calculated as the time from the 5-year follow-up assessment to event or censoring, because the exposed individuals were defined according to IBS symptoms at both baseline and 5-year follow-up. Individuals who had a diagnosis of a CMD (n = 249) or an FSS (n = 216) before the follow-up assessment were excluded. Furthermore, a total of 282 and 285 individuals were censored due to migration before the follow-up study, leaving 6,747 and 6,777 individuals for the primary analyses of CMDs and FSSs, respectively. Individuals were followed until first contact to the secondary health care system with a CMD or an FSS diagnosis and censored at first migration, death or December 31, 2013, whichever came first. Analyses were adjusted for cohort membership, which was created as a three-level variable consisting of Dan-MONICA 1 and Inter99 intervention group (A) and (B). Additionally, analyses were adjusted for age, sex and length of education. Mental vulnerability can be viewed as a confounder on the outcomes. In a subsequent analysis, we therefore adjusted the results for mental vulnerability and presented the results both with and without this additional adjustment. Furthermore, we conducted a sensitivity analysis where the item “Do you often have pain in different parts of your body, eg, your stomach, neck, back or chest?” was excluded from the 12-item mental vulnerability scale due to the possible symptom overlap with the abdominal pain item in the IBS definition. Moreover, we performed an additional Cox regression to investigate the associations between mental vulnerability and the outcomes. The associations were investigated both with and without taking IBS at baseline into account.

Ethical approval

Dan-MONICA 1 and Inter99 were approved by the local ethical committee at the time of data collection.21,22 The participants were informed that all information was to be used for research purposes only and gave written informed consent. The present study was approved by the Danish Data Protection Agency (2012-58-0009).

Results

The IBS symptom groups and the baseline characteristics are presented in Table 2. Further details can be found elsewhere.14 In the pooled cohort, 714 (10%) patients had IBS, 1,589 (22%) patients had IBS symptoms including abdominal pain, 1,276 (17%) patients had IBS symptoms without abdominal pain and 3,699 (51%) patients reported no IBS symptoms over the 5-year period. At baseline, mental vulnerability significantly increased with increasing fulfillment of the IBS definition. In total, 56% of patients with IBS were moderately/highly vulnerable, whereas 10% of those without IBS symptoms were moderately/highly vulnerable (Table 2).
Table 2

Irritable bowel symptom groups and baseline characteristics, pooled Dan-MONICA 1 and Inter99 cohort, n = 7,278

Baseline characteristicsIBS, n (%)IBS symptoms including abdominal pain, n (%)IBS symptoms without abdominal pain, n (%)Reference: no IBS symptoms, n (%)p
Pooled cohort714 (10)1,589 (22)1,276 (17)3,699 (51)
Dan-MONICA 1 cohort (n = 2,955)249 (8)724 (25)469 (16)1,513 (51)<0.001*
Inter99 cohort (n = 4,323)465 (11)865 (20)807 (19)2,186 (50)
Age (years)
Mean age (standard deviation)43.8 (8.6)44.5 (9.3)45.5 (9.0)46.6 (9.3)<0.001**
Sex
Women510 (71)910 (57)677 (53)1,517 (41)<0.001***
Men204 (29)679 (43)599 (47)2,182 (59)
Length of educationa
No/under educationb109 (16)246 (16)182 (15)458 (13)<0.001***
<2 years of education203 (30)554 (36)368 (30)1,161 (33)
2–4 years of education312 (46)632 (41)566 (46)1,565 (44)
>4 years of education50 (8)104 (7)104 (9)362 (10)
Mental vulnerabilityc
Highly vulnerable188 (26)211 (13)96 (7)88 (2)<0.001***
Moderately vulnerable209 (30)325 (21)225 (18)290 (8)
Not vulnerable315 (44)1,051 (66)955 (75)3,318 (90)

Notes:

Missing items on length of education (n = 302).

Individuals under education (n = 8) were categorized as individuals not having an education.

Missing items on mental vulnerability (n = 7).

Multinomial logistic regression adjusted for age and sex.

Kruskal–Wallis test.

Chi-square test.

Abbreviation: IBS, irritable bowel syndrome.

Development of CMDs and FSSs identified in secondary care

There was an increased risk of CMD development in secondary care both among individuals with IBS and IBS symptoms including abdominal pain (HR: 1.74 [95% CI: 1.18–2.56] and HR: 1.74 [95% CI: 1.31–2.31], respectively; Table 3) compared to individuals reporting no IBS symptoms. IBS symptoms without abdominal pain were not associated with subsequent registration of CMDs identified in secondary care (HR: 1.23 [95% CI: 0.87–1.73]; Table 3). When additionally adjusting the results for mental vulnerability, the HR estimates decreased, and overall, the IBS symptom groups were not significantly associated with CMD development in secondary care (Table 3). The sensitivity analysis using the reduced mental vulnerability scale showed an increased risk of CMD development among individuals with IBS symptoms including abdominal pain, but the overall association between symptom groups and the outcome remained insignificant. Across all symptom groups, depression, other anxiety, reaction to severe stress and adjustment disorders were the most frequent CMDs registered in secondary care (data not shown). There was an increased risk of FSS development in secondary care both among individuals with IBS and IBS symptoms including abdominal pain (HR: 1.94 [95% CI: 1.34–2.80] and HR: 1.76 [95% CI: 1.31–2.35], respectively; Table 4) compared to individuals reporting no IBS symptoms. IBS symptoms without abdominal pain were not associated with subsequent registration of FSSs identified in secondary care (HR: 1.32 [95% CI: 0.94–1.85]; Table 4). When additionally adjusting the results for mental vulnerability, the HR estimates decreased, but the overall association between symptom groups and the development of FSSs remained statistically significant (Table 4). The sensitivity analysis using the reduced mental vulnerability scale slightly increased the HR estimates, and the association remained significant (Table 4). In the registration of FSSs in secondary care, the syndrome codes were infrequently used compared to the unspecified symptom codes. Across all symptom groups, pain not elsewhere classified, myalgia/rheumatism unspecified and malaise and fatigue were the most frequently registered diagnoses (data not shown).
Table 3

Development of CMDs identified in secondary care for each irritable bowel symptom group, pooled Dan-MONICA 1 and Inter99 cohort

Irritable bowel symptom groupsCMDs, nHR (95% CI)a, n = 6,480b
pfHR (95% CI)c, n = 6,477d
pfHR (95% CI)c, n = 6,477d
pf
–MV adjustment+MV adjustment+MV adjustmente
IBS371.74 (1.18–2.56)1.06 (0.70–1.61)1.18 (0.78–1.77)
IBS symptoms including abdominal pain901.74 (1.31–2.31)1.31 (0.98–1.76)1.39 (1.04–1.87)
IBS symptoms without abdominal pain471.23 (0.87–1.73)1.11 (0.77–1.54)1.10 (0.78–1.56)
Reference: no IBS symptoms1161<0.00110.3210.17

Notes:

Adjusted for age, sex, length of education and study cohort.

Missing items on length of education (n = 267).

Adjusted for age, sex, length of education, study cohort and mental vulnerability.

Missing items on length of education (n = 267) and mental vulnerability (n = 3).

Reduced mental vulnerability scale without the item about pain in different parts of body, eg, stomach, neck, back and chest.

Cox regression: overall statistical association between symptom groups and CMDs.

Abbreviations: CMDs, common mental disorders; HR, hazard ratio; CI, confidence interval; MV, mental vulnerability; IBS, irritable bowel syndrome.

Table 4

Development of other FSSs for each irritable bowel symptom group, pooled Dan-MONICA 1 and Inter99 cohort

FSSs, nHR (95% CI)a, n = 6,507b
pfHR (95% CI)c, n = 6,504d
pfHR (95% CI)c, n = 6,504d
pf
–MV adjustment+MV adjustment+MV adjustmente
IBS431.94 (1.34–2.80)1.48 (1.00–2.20)1.63 (1.11–2.40)
IBS symptoms including abdominal pain831.76 (1.31–2.35)1.52 (1.12–2.06)1.60 (1.19–2.16)
IBS symptoms without abdominal pain491.32 (0.94–1.85)1.21 (0.86–1.71)1.26 (0.90–1.77)
Reference: no IBS symptoms1161<0.00110.04310.010

Notes:

Adjusted for age, sex, length of education and study cohort.

Missing items on length of education (n = 270).

Adjusted for age, sex, length of education, study cohort and mental vulnerability.

Missing items on length of education (n = 270) and mental vulnerability (n = 3).

Reduced mental vulnerability scale without the item about pain in different parts of body, eg, stomach, neck, back and chest.

Cox regression: overall statistical association between symptom groups and FSSs.

Abbreviations: FFSs, functional somatic syndromes; HR, hazard ratio; CI, confidence interval; MV, mental vulnerability; IBS, irritable bowel syndrome.

There was no statistically significant interaction between the IBS symptom groups and cohort membership on any outcome (p > 0.05). A high/moderate mental vulnerability was statistically significantly associated with subsequent CMDs and FSSs (HR: 2.72 [95% CI: 2.14–3.45] and HR: 1.97 [95% CI: 1.54–2.52], respectively). When accounting for the IBS symptom group at baseline, the estimates slightly decreased (HR: 2.53 [95% CI: 1.96–3.26] and HR: 1.72 [95% CI: 1.32–2.24], respectively), but the overall significant association between mental vulnerability and the outcomes remained (both p < 0.001).

Discussion

Individuals both fulfilling and not fulfilling the IBS definition but who reported IBS symptoms including abdominal pain more often developed CMDs and FSSs identified in second ary care compared to individuals reporting no IBS symptoms. Individuals with IBS symptoms without abdominal pain were not associated with subsequent CMDs or FSSs. When accounting for mental vulnerability, the estimates decreased and only the associations between IBS, IBS symptoms including abdominal pain and the development of other FSSs remained significant.

Interpretation and explanation of the findings

Mental vulnerability is defined as a low threshold for susceptibility.38 Psychometric evaluation has shown that the 12-item mental vulnerability scale has a strong association with somatization and the personality trait neuroticism.17 Somatization refers to a tendency to experience and communicate somatic distress in response to psychosocial stress and seek medical help for it.39 Neuroticism is widely defined as a tendency to experience negative emotions and bodily sensations, especially when threatened, frustrated or facing loss.18 In this study, mental vulnerability showed to be a strong predictor of both outcomes, independent of the presence of IBS. The primary results indicated that when accounting for the tendency to be mentally vulnerable, individuals reporting IBS symptoms in a general population were not more likely to be classified in secondary health care with CMDs than individuals without IBS symptoms. In addition, both neuroticism and somatization have been linked to explain the frequent comorbid symptoms and related functional comorbidities of IBS.4,20 Our study indicated that the association between IBS symptoms and the subsequent registration of other FSSs could not be explained by mental vulnerability only.

Relation to other studies

In this longitudinal study of a general adult Danish population, we found that 10% fulfilled the definition of IBS over a 5-year follow-up period. Moreover, 56% of these individuals reported comorbid symptoms and traits equivalent to a moderate or high mental vulnerability. Mental vulnerability has been shown to be a predictor of increased health care use and a broad variety of health outcomes.37,40,41 In this study, we confirmed previous longitudinal findings that IBS is associated with subsequent development of CMDs.9,11,12 For example, a large register-based study from Taiwan showed an increased risk of depression, anxiety, sleep and bipolar disorders following a diagnosis of IBS.9 However, the study was based on a selected patient population newly diagnosed with IBS caused by gastroenteritis. In our population-based sample, we showed this increased risk also among individuals not fulfilling the symptom cluster of IBS over a 5-year period but who reported frequent abdominal pain. A recent nationwide Italian cohort study found a significant relationship between migraine/headache, IBS and fatigue among primary care patients and later development of depressive disorders in general practice.42 Our study added that the increased risk of CMDs in secondary care is likely to be explained by subgroups of individuals with IBS symptoms who also are mentally vulnerable. An 8-year follow-up study of 493 Swedish IBS patients identified in primary care showed a similar mental and functional comorbidity pattern in secondary care compared to our study.10 However, the two studies were difficult to compare due to different methods, differences in delimitation of IBS and lack of information about the specific register diagnoses used. In our population-based study, we showed an increased risk of FSS development also among individuals not fulfilling the IBS definition over a 5-year period but who reported frequent abdominal pain. These findings support the growing recognition that there is a significant overlap among FSSs with persistent pain as a predominant feature. Moreover, there has been a growing recognition of a shared underlying mechanism, primarily central sensitization of the central nervous system.43 In addition, bidirectional communication from the gut to the brain and from the brain to the enteric nervous system is likely to explain symptoms outside the gastrointestinal system.44 Although the precise mechanisms are not fully understood, it is possible that these “gut–brain” pathways play a role in the development of mental comorbidity and functional comorbidity at least in subgroups of patients with IBS.

Methodological considerations

Until now, few population-based studies have investigated the associations between IBS and subsequent CMDs and FSSs identified in secondary care. Furthermore, none of these studies have included mental vulnerability or performed subgroup analyses based on the nature of IBS symptom reporting.9–12 In this study, the exposure was based on the 5-year follow-up period and we focused on the long-term incidence of CMDs and FSSs in the two time periods 1987–2014 and 2004–2014. The linkage to Danish national registers ensured accurate and precise information about deaths, migration and date of first hospital contact with a specific diagnostic code. The diagnoses in the registers were registered by medical specialists in secondary care. The available data were not collected to define IBS according to the present Rome IV criteria.8 The Rome criteria developed at the time of data collection were not sufficient to define IBS in a general population (abdominal pain was not mandatory and the criteria did not require any frequency of symptoms).45 Therefore, we used an IBS definition defined according to valid statistical criteria in population-based data.25,46 However, it was a limitation that we only had information on self-reported IBS symptoms in the past 12 months and no information on symptom duration and severity. This could have introduced some misclassification of IBS. Nevertheless, in this study, we focused on self-reported IBS symptoms in a general population and not on incident IBS patients. With this symptom approach, we did not delimitate IBS from other functional gastrointestinal disorders. The focus on IBS symptoms among individuals participating in two general health examinations could have introduced some selection bias toward a more healthy population sample. Some of the nonparticipants and the nonattenders to the 5-year follow-up studies could have been individuals with persistent and severe symptoms. Moreover, the exclusion of previous diagnoses with CMDs and FSSs could have excluded the most vulnerable individuals. This could imply an underestimation of the association between fulfillment of IBS and the outcomes. The possible selection bias may be largest in the Inter99 study due to the low participation rate and its intervention design. However, we found no significant interaction between cohort membership and the IBS symptom groups in relation to the outcomes, indicating that this selection bias was of lower importance. Nevertheless, Koloski et al. have shown that gut-brain pathways in IBS are bi-directional.12 Therefore, the study design limited the focus to individuals with IBS developing mental and functional comorbidities later in life. Individuals were randomly selected from the CRS and were therefore equally likely to be selected to the study. However, only individuals of age 30–60 years were invited, and individuals not of Danish nationality were excluded, because the study is primarily generalizable to an adult Danish-speaking population. In relation to the outcomes, we only had information about severe CMDs treated in secondary care and we did not have information about milder versions of these conditions treated in primary care. Moreover, the registration practice of FSSs across medical specialties is unclear and may have changed over time. We addressed this limitation by including unspecific symptom diagnoses in our delimitation of FSSs. As expected, the syndrome diagnoses were infrequently used compared to the unspecific symptom diagnoses. Finally, we included few potential confounders due to uncertainties about risk factors to IBS and did not address other possible explaining factors such as gastrointestinal infections,16 food intolerances47 and use of medicine.48

Conclusion and implications

Mental vulnerability may explain the increased risk of CMD development in secondary care among individuals reporting IBS symptoms. Moreover, individuals with abdominal pain including those fulfilling the IBS definition have an increased risk of FSS development in secondary care, and this association cannot be explained by mental vulnerability only. These findings support the recognition of a significant overlap among FSSs. In a clinical setting, it is important to broaden the perspective to patients not fulfilling the symptom cluster of IBS and especially patients reporting frequent abdominal pain. Additionally, it is important to combine symptom-based criteria of IBS with psychosocial markers such as mental vulnerability, because it could guide clinicians in decisions regarding prognosis and treatment. The 12-item mental vulnerability scale
Table S1

The 12-item mental vulnerability scale

We would like to ask you some questions regarding your personal well-being. Please do not think too much about the answers – just answer as you find most suitable
1. Do your hands easily shake?
2. Do you often suffer from loss of appetite?
3. Do you often suffer from sleeplessness?
4. Do you often feel very tired?
5. Do you often take medicine, such as headache tablets, sleeping pills, tranquilizers or the like?
6. Do you often have pain in different parts of your body, eg, your stomach, neck, back or chest?
7. Do you often suffer from fits of dizziness?
8. Does your heart often beat very fast for no particular reason?
9. Is it difficult for you to make friends?
10. Do small things get on your nerves?
11. Do you constantly have thoughts which trouble and worry you?
12. Do you usually feel misunderstood by other people?
  45 in total

1.  Rome IV-Functional GI Disorders: Disorders of Gut-Brain Interaction.

Authors:  Douglas A Drossman; William L Hasler
Journal:  Gastroenterology       Date:  2016-05       Impact factor: 22.682

2.  Mental vulnerability as a risk factor for depression: a prospective cohort study in Denmark.

Authors:  Ditte Østergaard; Susanne Oksbjerg Dalton; Pernille Envold Bidstrup; Aslak Harbo Poulsen; Kirsten Frederiksen; Lene Falgaard Eplov; Christoffer Johansen; Erik Lykke Mortensen
Journal:  Int J Soc Psychiatry       Date:  2011-03-25

3.  The brain--gut pathway in functional gastrointestinal disorders is bidirectional: a 12-year prospective population-based study.

Authors:  N A Koloski; M Jones; J Kalantar; M Weltman; J Zaguirre; N J Talley
Journal:  Gut       Date:  2012-01-10       Impact factor: 23.059

4.  The Danish Psychiatric Central Research Register.

Authors:  Ole Mors; Gurli P Perto; Preben Bo Mortensen
Journal:  Scand J Public Health       Date:  2011-07       Impact factor: 3.021

5.  The Danish Civil Registration System.

Authors:  Carsten Bøcker Pedersen
Journal:  Scand J Public Health       Date:  2011-07       Impact factor: 3.021

6.  Evidence that independent gut-to-brain and brain-to-gut pathways operate in the irritable bowel syndrome and functional dyspepsia: a 1-year population-based prospective study.

Authors:  N A Koloski; M Jones; N J Talley
Journal:  Aliment Pharmacol Ther       Date:  2016-07-22       Impact factor: 8.171

7.  Epidemiology of upper dyspepsia in a random population. Prevalence, incidence, natural history, and risk factors.

Authors:  L Kay; T Jørgensen
Journal:  Scand J Gastroenterol       Date:  1994-01       Impact factor: 2.423

8.  Incidence of gallstones in a Danish population.

Authors:  K H Jensen; T Jørgensen
Journal:  Gastroenterology       Date:  1991-03       Impact factor: 22.682

Review 9.  The epidemiology of irritable bowel syndrome.

Authors:  Caroline Canavan; Joe West; Timothy Card
Journal:  Clin Epidemiol       Date:  2014-02-04       Impact factor: 4.790

10.  Effect of screening and lifestyle counselling on incidence of ischaemic heart disease in general population: Inter99 randomised trial.

Authors:  Torben Jørgensen; Rikke Kart Jacobsen; Ulla Toft; Mette Aadahl; Charlotte Glümer; Charlotta Pisinger
Journal:  BMJ       Date:  2014-06-09
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  4 in total

Review 1.  Extraintestinal manifestations in irritable bowel syndrome: A systematic review.

Authors:  Bodil Ohlsson
Journal:  Therap Adv Gastroenterol       Date:  2022-08-09       Impact factor: 4.802

2.  Irritable bowel syndrome in women: Association between decreased insular subregion volumes and gastrointestinal symptoms.

Authors:  Nawroz Barazanji; J Paul Hamilton; Adriane Icenhour; Rozalyn A Simon; Olga Bednarska; Sofie Tapper; Anders Tisell; Peter Lundberg; Maria Engström; Susanna Walter
Journal:  Neuroimage Clin       Date:  2022-07-28       Impact factor: 4.891

3.  Leveraging 16S rRNA Microbiome Sequencing Data to Identify Bacterial Signatures for Irritable Bowel Syndrome.

Authors:  Yuxia Liu; Wenhui Li; Hongxia Yang; Xiaoying Zhang; Wenxiu Wang; Sitong Jia; Beibei Xiang; Yi Wang; Lin Miao; Han Zhang; Lin Wang; Yujing Wang; Jixiang Song; Yingjie Sun; Lijuan Chai; Xiaoxuan Tian
Journal:  Front Cell Infect Microbiol       Date:  2021-06-11       Impact factor: 5.293

4.  The impact of mental vulnerability on the relationship between cardiovascular disease and depression.

Authors:  Terese Sara Høj Jørgensen; Marie Kim Wium-Andersen; Martin Balslev Jørgensen; Merete Osler
Journal:  Eur Psychiatry       Date:  2020-02-14       Impact factor: 5.361

  4 in total

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