Skip to main content
Gastroenterology Research and Practice logoLink to Gastroenterology Research and Practice
. 2015 Dec 31;2016:3186016. doi: 10.1155/2016/3186016

Functional Constipation and Constipation-Predominant Irritable Bowel Syndrome in the General Population: Data from the GECCO Study

Paul Enck 1,*, Johannes Leinert 2, Menno Smid 2, Thorsten Köhler 2, Juliane Schwille-Kiuntke 1
PMCID: PMC4736007  PMID: 26880887

Abstract

Background. The prevalence of constipation in the (German) population has been shown to be 14.9% in a telephone survey, but more detailed data are required to characterize the sociographics and clinical characteristics of persons with different types of functional constipation, either constipation-predominant irritable bowel syndrome (IBS-C) or functional constipation with or without meeting Rome criteria. Methods. Of 2239 constipated individuals identified during the telephone interview, 1037 (46.3%) were willing to provide a postal address for a questionnaire, of which 589 (56.8%) returned the questionnaire, inquiring about sociographic data, clinical symptoms, and health care behavior related to constipation, as well as health-related quality-of-life (SF12). Subgroups of functionally constipated individuals were compared. Results. More than 50% of the respondents reported a somatic comorbid condition and/or regular medication intake that may contribute to constipation. We split the remaining individuals (N = 214) into three groups, matching Rome-criteria for IBS (IBS-C, n = 64) and for functional constipation (FC-R, n = 36) and FC not matching Rome criteria (n = 114). Nearly all sociographic and clinical characteristics were equal among them, and all individuals with constipation had similar and lowered QOL on the SF-12 physical health domain, but in IBS-C the scores were also significantly lower in comparison to FC-R and FC, in both the physical health and the mental health domain. Conclusion. Only a fraction of individuals with chronic constipation match Rome criteria for IBS-C or FC, but subgroups do not differ with respect to most other measures except quality-of-life profiles.

1. Background

Prevalence of chronic constipation has been reported to range between 5% and 15% of the general population, depending on the size and type of assessment, the definition of constipation, and variables such as nationality, culture, and the health care system [13]. In a recent paper we reported constipation to be 14.9% [4] in a representative sample from Germany, which is almost identical with the 14% reported pooled prevalence across 41 studies worldwide [5].

Constipation-predominant IBS (IBS-C) represents a subgroup of all IBS patients in whom abdominal pain is associated with constipation, while other predominant bowel symptoms (diarrhea, alternating diarrhea, and constipation) are labeled as IBS-D and IBS-M [6] when matching Rome criteria for IBS definitions [7]. Another Rome-defined functional bowel disorder with constipation as predominant symptom is “functional constipation” (FC-R). This definition requires not classifying for IBS-C, and at least 2 of six symptoms (need for straining, lumpy or hard stools, sensation of incomplete evacuation, sensation of anorectal obstruction, and need for manual maneuvers to facilitate defecation more than occasionally) or less than 3 defecations/week. Since constipation is (at least in epidemiological surveys) symptom-based and self-defined, there may as well be a group of people that perceive themselves as being constipated without matching Rome or other criteria [7], for example, reporting no abdominal pain or none of the additionally required symptoms. All these subgroups may be labeled “functional constipation”; their differential clinical phenotypes have only occasionally been described.

When patients with IBS-C were compared to patients with functional constipation matching or not matching Rome criteria, Rey et al. [6] found patients with painful or painless constipation not matching IBS-C criteria to be moderately younger and more frequently consulters in comparison to IBS-C, while Zhao et al. [8] comparing IBS-C to functional non-IBS constipation showed IBS-C to have a lesser need to strain but more incomplete evacuations after defection. Only the mental health subscale of the SF-36 was significantly lowered in IBS-C. Some differences were found with respect to upper GI symptoms: Koloski et al. [9] compared patients meeting Rome criteria for functional to patients with IBS-C and found only higher age at constipation onset, less likelihood to exercise, and higher mental health compared to IBS-C. Finally, Heidelbaugh et al. [10] compared patients with chronic idiopathic constipation with or without abdominal pain and IBS-C patients and found both IBS-C and chronic idiopathic constipation patients with pain significantly more bothered than constipation patients without pain.

Constipation may also occur as a secondary symptom, for example, in a number of neurological (e.g., stroke, Parkinson's disease, and spinal cord injury), systemic (diabetes, hypothyroidism, and scleroderma), and other disorders, to intestinal or nonintestinal surgery [1113] or to a variety of medications used for treatment of chronic clinical conditions, for example, calcium antagonists for high blood pressure [14], opioids for chronic pain [15], and tricyclic antidepressants for major depression [16].

Quality-of-life (QoL) has been reported to be low in functional constipation as well as in IBS-C when assessed with both constipation-specific QoL instruments [17] and generic QoL tests in comparison to other chronic conditions [18, 19]; however they have yet not been compared between subgroups (except [6, 8]).

The purpose of the present evaluation of the German Chronic Constipation (GECCO) study data was to compare different populations with functional constipation with or without abdominal pain with respect to sociographic, clinical, and quality-of-life data. We assumed representativeness of our samples allowing conclusions on the population prevalence of the different subgroups but tested for response biases beforehand.

2. Methods

The aim of GECCO study was to (a) determine the prevalence of chronic constipation among adults in Germany and (b) obtain information on their quality-of-life and further medical parameters by a subsequent written survey. The prevalence data from a telephone interview with 15.000 representative adults were recently [4] reported.

The 10-minute interview concluded with sociographic data (education and training, professional status, and family income). Only if constipation had been acknowledged were they asked whether they would provide a postal address for sending a more elaborate questionnaire on this topic.

2.1. The Questionnaire

The 8 pages' (37 + 3 items) questionnaire was sent within 2 weeks following the interview. If the questionnaire was not sent back (by a prepaid envelop) within 3 weeks, a reminding letter was sent to the person to ask for completion; a second reminding letter would follow if again no response occurred within three weeks.

The questionnaire was composed of 4 modules (1: General Health; 2: Concurrent Diseases/Medication; 3: Health Care Utilization; 4: Constipation and IBS) and started with some general questions to overall health that contained the items of the Short-Form 12 (SF-12) [20]. Module 2 inquired about the presence of pregnancy and of GI and non-GI diseases (Crohn's disease, ulcerative colitis, GI cancer, celiac disease, and prolapse) and nonintestinal disorders (diabetes, hypothyroidism, stroke, Parkinson's disease, multiple sclerosis) (yes, no) that are frequently associated with constipation and about medication intake of the most frequent drugs (generic and brands) on the German market (contraceptives, beta-blockers, ACE inhibitors, calcium antagonists, diuretics, statins, L-thyroxin, antidiabetics, PPI, pain medication, antidepressants, barbiturates, and sedatives), each to be answered for their frequency (daily, at least twice/week, and less). Similarly, drugs taken for constipation (macrogol, lactulose, sorbitol, bisacodyl, sodium bicarbonate, prucalopride, psyllium, senna, and Glauber's salt) were checked for intake frequency (daily, at least twice/week, and less), efficacy, and side effects. Patients were also asked for changes of nutritional habits because of constipation.

Module 3 inquired about consultation of specialists in the past 12 months, sick-days because of constipation, inpatient treatment, diagnostic procedures performed, and complementary and alternative remedies taken because of CC, including the amounts spent that were not reimbursed by health insurance plans. These data will be reported in a separate paper.

Module 4 contained questions from the Rome III modular questionnaire for IBS and for functional constipation [7].

Final three questions referred to statistics and the willingness to participate in a future follow-up questionnaire study.

The protocol of the study methodology had been reviewed by the Ethics Committee of the Tübingen University Medical School, and the study was conducted in accordance with approved standards for epidemiological research [21].

2.2. Statistics

Usually, response rates are reported and used without additionally checking for the representativeness of the cohort. To control for potential self-selection biases in the questionnaire data, we compared individuals with constipation who provided a postal address for sending the questionnaire to those that refused to participate with respect to the sociographic data available from the interview. We also compared those that returned the questionnaire to those that did not, using the same data set. These comparisons were done by groupwise t-tests and chi-square tests, where appropriate.

Constipation subsamples were constructed based on predefined criteria: patients with at least one somatic diagnosis and/or more than twice weekly intake of medication for nonconstipation reasons constituted a group labeled “constipation probably associated with a somatic condition” (= putative comorbid constipation) and were excluded from the present analysis; we will report these data in a separate paper.

Among the remaining cases, those meeting Rome III criteria for IBS (based on the algorithm provided by the Rome committee [7]) were labeled IBS-C, those meeting Rome criteria for functional constipation but not IBS-C were called FC-R, and the remaining cases were labeled FC. Subgroups were compared by parametric (ANOVA) and nonparametric tests (chi-square test) where appropriate.

All data are reported as mean ± SD and are unweighted with respect to the initial representative survey. The significance level was set to 0.05 for all tests. Post hoc t-tests and chi-square test of subgroup comparisons were not corrected for multiple comparisons but instead only performed when the main (ANOVA, chi-square test) analysis was significant.

3. Results

During the telephone survey [4], we identified 2239 individuals acknowledging the presence of constipation symptoms during the preceding 12 months [4]. Of these, 1037 (46.3%) were willing to provide a postal address and were sent the questionnaire. Of these 1037 individuals, 589 returned the questionnaire and provided useable data (56.8%).

3.1. Self-Selection Bias Control

We compared the data available from the telephone survey [4] between those constipated individuals that would (n = 1037) or would not (n = 1202) provide a postal address for sending the questionnaire and between those that did (n = 589) or did not (n = 448) return the questionnaire (see Table 1).

Table 1.

Test for self-selection biases between those providing a post address for sending the questionnaire and those who did not and between those who send back the questionnaire and those who did not. Compared are the data provided during the telephone interview prior to asking for the postal address. Data are unweighted.

Questionnaire received Questionnaire returned
Yes: n = 1037 No: n = 1203 Stats Yes: n = 589 No: n = 448 Stats
Personal data
Age (mean, SD) 51.3 ± 0.6 49.9 ± 0.6 n.s. 55.3 ± 0.7 46.0 ± 0.9 p < 0.001
Male : female 352 : 685 453 : 750 n.s. 201 : 388 151 : 297 n.s.
Height (m) 1.69 ± 0.01 1.69 ± 0.01 n.s. 1.69 ± 0.01 1.69 + 0.01 n.s.
Weight (kg) 74.6 ± 0.5 74.9 ± 0.2 n.s. 74.7 ± 0.7 74.5 ± 0.9 n.s.
BMI 26.1 ± 0.2 25.9 ± 0.1 n.s. 26.2 ± 0.2 26.0 ± 0.3 n.s.

Social situation
Education: secondary+ 256 284 n.s. 155 101 p = 0.010
Full-time/part time (1) 375 449 1/2 versus 3/5
4 excluded:
n.s.
195 179 1/2 versus 3/5
4 excluded:
p = 0.016
Mini job, occasional (2) 72 86 46 27
Not working, training (3) 186 244 94 92
Parent time (4) 54 39 18 35
Retired (5) 347 379 234 113
Income: >2,500€/mo 284 221 160 123 n.s.

Life satisfaction
Fully (1) 309 350 1/2 versus 3/4:
p < 0.001
186 123 1/2 versus 3/4:
p = 0.007
Rather (2) 531 689 308 223
Rather not (3) 134 111 68 66
Not at all (4) 59 49 25 34

General health
Very good (1) 111 141 1/2 versus 3/4/5:
n.s.
63 48 1/2 versus 3/4/5:
n.s.
Good (2) 360 421 217 143
Satisfactory (3) 305 351 168 137
Less good (4) 166 176 91 74
Bad (5) 90 113 48 43

Health problems
Sick the last 4 wks: no 705 899 p < 0.001 410 295 n.s.
Back pain: yes 684 771 n.s. 390 293 n.s.
Circulation: yes 433 486 n.s. 225 208 p = 0.008
Gynacological: yes 106/685 91/750 n.s. 61/388 44/297 n.s.
Urological: yes 145 156 n.s. 82 63 n.s.
Gastrointestinal: yes 330 377 n.s. 189 141 n.s.

Constipation characteristics
Duration (years) 9.7 ± 0.5 9.2 ± 0.5 n.s. 11.3 ± 0.7 7.8 ± 0.6 p < 0.001
12 months' prevalence 614 762 p = 0.042 352 262 n.s.
4 weeks' prevalence 422 441 p = 0.052 237 185 n.s.
Acute constipation 196 191 p = 0.047 104 92 n.s.
To doctor 240 200 p < 0.001 131 109 n.s.
Medication 353 345 p = 0.004 194 159 n.s.
<3 stools/week 380 398 p = 0.055 199 181 p = 0.029
Straining 659 653 p < 0.001 388 271 n.s.
Hard stools 764 830 p = 0.005 439 325 n.s.

+Number with secondary school finished (maturation); Statistics: t-test or chi-square test; n.s.: not significant.

As can be seen, the two steps (accepting the questionnaire to be sent and returning the questionnaire) generated two distinct self-selection biases in the sample: the first with respect to the severity of the constipation symptoms and the latter with respect to the age and health comorbidity conditions. Patients with more severe constipation symptoms, more acute problems, more medication intake and doctor visits because of constipation, and a higher burden by different constipation symptoms were more willing to provide further information and accepted the questionnaire to be sent.

After they had received the questionnaire, another self-selection bias is apparent: those that returned the questionnaire were on average 10 years older than those that did not respond, and this was associated with a higher percentage being retired, having lower overall life satisfaction, additional (circulation) problems, and a longer duration of constipation. However, second, this self-selection was not based on constipation symptom severity.

3.2. IBS-Associated Symptoms in Functional Constipation

Table 2 shows the distribution of the 589 respondents across the IBS and functional constipation-associated symptoms as defined by the Rome criteria.

Table 2.

IBS and constipation symptoms according to the Rome Modular Questionnaire (RMQ) (validated German version). Absolute number of respondents is given. Please note that the sequence of questions was different than in the RMQ because all participants were asked for their constipation symptoms first (52–58, 59), followed by the abdominal pain/discomfort questions (41, 45, 43, 46–50, and 44). Data are unweighted.

RMQ item Question Number of respondents (N = 589)+
Frequency of symptoms 0 1 2 3 4
52 Less than 3 stools/week 312 128 72 28 20
53 Hard or lumpy stools 107 262 117 59 7
54 Straining for stools 92 226 132 66 31
55 Feeling of incomplete evacuation 143 222 143 34 12
56 Obstructed defecation 257 193 77 23 7
57 Digital manipulation needed 321 161 41 12 6
58 Problems to relax for evacuation 226 233 59 20 9
46 Pain improved w/defecation 73 95 100 126 96
47 Onset associated w/defecation 264 126 35 39 12
48 Less stools with pain/discomfort 231 148 44 28 13
49 Softer stool with pain/discomfort 202 149 47 56 16
50 Harder stools w/pain/discomfort 165 172 86 53 13
44 Pain/discomfort affecting daily life 251 195 70 17 8
59 Constipation starting > 6 months No: 203 Yes: 339
Frequency# 0 1 2 3 4 5 6
41 Abdominal pain/discomfort 149 97 46 129 61 71 17
45 Pain/discomfort for > 6 months No: 238 Yes: 301
43 Associated w/menstruation° No: 211 Yes: 37

0: never or rarely; 1: sometimes; 2: often; 3: almost always; 4: always; #0: never; 1: <1 day/month; 2: 1 day/month; 3: 2-3 days/month; 4: 1 day/week; 5: >1 day/week; 6: every day; +remainder to 586 are missing/no response; °only women (N = 297).

All symptoms associated with IBS are present to an almost equal extent, and similarly all constipation symptoms are. Also, abdominal pain and discomfort was reported by 4/5, but only a small fraction (approx. 25%) experienced abdominal pain/discomfort at least once a week or more, thus matching the minimal requirement for IBS.

3.3. Comorbid Constipation

Among all 589 respondents, 9 women acknowledged being pregnant—they were excluded—leaving 580 data sets to be entered into this analysis.

When asked for concurrent GI and non-GI diagnoses, 245 persons reported one or more diagnoses to be present, and in 314 cases medication was taken at least twice per week, resulting in 366 cases of putative “comorbid constipation” (62.9%). The data of this subsample were excluded from this analysis but will be reported in a separate paper. The 214 remaining cases of “functional constipation” (38.1%) were included and are presented here.

3.4. Functional Constipation (IBS-C versus FC-R versus FC)

Of all patients with assumed nonsomatic (“functional”) constipation (n = 214), n = 64 (11.0% of the total cohort of n = 580) met criteria for IBS-C according to the Rome III definition [7], that is, abdominal pain/discomfort at least 3 days per month in addition to constipation, for more than 6 months, not associated with the menstrual cycle, and at least 2 of the following symptoms: symptom improvement with defecation, onset associated with a change in stool frequency, and onset associated with a change in stool form. Of the remaining cases, n = 36 (6.2%) met Rome III criteria for functional constipation (FC-R): not meeting the criteria for IBS-C, and at least 2 of the following six symptoms: need for straining, lumpy or hard stools, sensation of incomplete evacuation, sensation of anorectal obstruction, and need for manual maneuvers to facilitate defecation more than occasionally, or less than 3 defecations/week. The remaining 114 cases (19.7%) were classified as “functional constipation” (FC).

Age and sex distribution were similar in all three groups (Table 3) as were social factors (education, income, and job situation).

Table 3.

Sociographic data and health problems and life satisfaction in functionally constipated participants (n = 214) in the telephone survey by type of constipation (IBS-C, FC-R, and FC—see text for definitions). Data are unweighted.

Variable name IBS-C, N = 64 FC-R, N = 36 FC, N = 114 Statistics#
ANOVA or chi-square Pairwise post hoc test
1-2 1–3 2-3
Personal data
Age (mean, SD) 44.1 ± 1.6 44.6 ± 2.9 43.2 ± 1.5 n.s.
Male : female 17 : 47 12 : 24 41 : 73 n.s.
Height (m) 1.70 ± 0.01 1.68 ± 0.02 1.70 ± 0.01 n.s.
Weight (kg) 72.0 ± 2.2 65.9 ± 1.9 72.2 ± 1.5 n.s.
BMI 24.7 ± 0.6 23.3 ± 0.5 24.8 ± 0.5 n.s.

Social situation
Education: secondary+ 27 9 39 n.s.
Full-time/part time (1) 31 25 56 1/2 versus 3/5
4 excluded:
n.s.
Mini job, occasional (2) 9 5 11
Not working, training (3) 13 3 12
Parent time (4) 3 0 9
Retired (5) 8 3 16
Income: >2,500€/mo 24 17 39 n.s.

Life satisfaction
Fully (1) 15 14 40 1/2 versus 3/4:
p = 0.048
n.s. n.s.
Rather (2) 36 21 59
Rather not (3) 7 1 15
Not at all (4) 6 0 0

General health
Very good (1) 13 6 30 1/2 versus 3/4/5:
n.s.
Good (2) 28 20 52
Satisfactory (3) 12 8 21
Less good (4) 8 3 9
Bad (5) 4 0 2

Health problems
Sick the last 4 wks: no 48 33 93 n.s.
Back pain: yes 43 22 59 n.s.
Circulation: yes 22 10 21 n.s.
Gynacological: yes 8/47 1/24 12/73 n.s.+
Urological: yes 1 4 8 n.s.+
Gastrointestinal: yes 29 9 22 p < 0.001 n.s. ∗∗∗ n.s.

#ANOVA: univariate, 3 groups, or 2 × 3 chi-square: in case of significance, pairwise post hoc comparisons; +number with secondary school finished (maturation); ∗∗∗post hoc testing: ∗∗∗ p < 0.001; ∗∗ p < 0.01; p < 0.05; +Fisher's Exact Test; n.s.: not significant.

When asked for their acute health problems, again no major differences occurred between the functional constipation subgroups except that significantly more gastrointestinal symptoms beyond constipation were reported in individuals with IBS-C as compared to FC.

As shown in Table 4, no differences were found for the duration of constipation, doctor visits for constipation during the last 12 months, and medication intake for constipation. While an equal number of the constipated individuals report the presence of hard stools, stool frequency lower than 3/week and straining were more present in the IBS-C and FC-R group as compared to FC.

Table 4.

Clinical data and health care behaviors in the functionally constipated participants (n = 214) in the questionnaire by type of constipation (IBS-C, FC-R, and FC—see text for definitions). Data are unweighted.

IBS-C, N = 64 FC-R, N = 36 FC, N = 114 Statistic#
ANOVA Post hoc test
1-2 1–3 2-3
Constipation characteristics
Duration of C (in years) 9.1 ± 1.4 9.6 ± 2.4 8.6 ± 1.2 n.s.
To doctor for C: yes 13 2 15 n.s.
Medication for C: yes 21 6 23 n.s.
<3 stools/w: yes 27 19 32 p = 0.004 n.s. ∗∗
Straining: yes 51 20 65 p = 0.006 ∗∗ n.s.
Hard stools: yes 54 28 79 n.s.

Health care behaviors
Current medication: yes 11 8 11 n.s.
Does it help: yes 11 8 11 n.s.
Side effects: yes 14 (11) 5 11 n.s.
Changed diet: yes 41 21 36 p < 0.001 n.s. ∗∗∗ ∗∗
Sick leave for C: yes 4 0 6 n.s.+
Inpatient for C: yes 0 0 2 n.s.+
CAM for C: yes 13 4 6 p = 0.008 n.s. ∗∗ n.s.
Currently working: yes 43 28 78 n.s.
Yes: clean WC available∗∗ 37 25 65 n.s.+
Yes: WC visit any time∗∗ 12 10 32 n.s.

C: constipation; CAM: complementary and alternative medicine; #ANOVA: univariate, 3 groups, or chi-square: “IBS” versus “functional constipation” (FC-R + FC): only in case of significance, pairwise post hoc comparisons; only those who take meds; ∗∗only those who are working; ∗∗∗post hoc testing: ∗∗∗ p < 0.001; ∗∗ p < 0.01; p < 0.05; +Fisher's Exact Test; n.s.: not significant.

Current medication intake for constipation was similar for IBS-C (17.2%), FC-R (22.2%), and FC (9.6%) (Table 3), but complementary and alternative medicines (CAM) (homeopathy, acupuncture, and Chinese herbal medicines) for constipation were used by more IBS-C than FC individuals (20.3, 11.1, and 5.2%, resp., p = 0.008). A majority of individuals with IBS-C and FC-R claimed to have changed diet to counteract constipation (64.1, 58.3, and 31.6%, resp., p < 0.001), and the dietary actions include all measures listed in the questionnaire (more vegetables, more legumes, liquid intake, probiotics, etc.).

Individuals with constipation had similar and lowered QoL on the SF-12 physical health domain in all three groups (IBS-C, FC-R, and FC) compared to population norms of the test, but in IBS-C the scores were also significantly lower in comparison to FC-R and FC, in both the physical health and the mental health domain (Figure 1).

Figure 1.

Figure 1

Quality-of-life in groups of constipated participants (individuals with IBS-C, FC-R, and FC, see text for definitions) as measured by the SF-12 (arbitrary units, mean ± SD) in the physical domain (a) and the mental domain (b). F-values indicate significance in the between-group ANOVA. “” indicating significance in post hoc t-tests (uncorrected): ∗∗∗ p < 0.001; ∗∗ p < 0.01; p < 0.05.

4. Discussion

Comparing the responses of individuals reporting to have been constipated in the past 12 months during a telephone interview [4] and after returning a mailed questionnaire, we found only half of the sample to have functional constipation while in the remaining coexistence of somatic disorders (and respective medication intake) may contribute to the constipation symptoms. In search for possible explanations for this effect that has not been described in previous reports, we performed a bias analysis by comparing those that accepted a follow-up questionnaire and those that did not, as well as between those that returned the questionnaire and those that did not. Such post hoc self-selection bias analyses have rarely been reported in previous population surveys on constipation, IBS, and related gastrointestinal issues; they are, however, known from other epidemiological health surveys [22] and assessments of screening programs [23], for example, in the area of pain, cancer, and sexuality [24, 25], and are subject to statistical research on potential correction factors [26]. Usually, response rates are reported and used as if not affecting the representativeness of the cohort. However, as we show here, a strong self-section bias was apparent in our sample: elderly people especially with somatic comorbidity chose to return the questionnaire, while younger ones are underrepresented. We are not reporting the data of this subsample of “somatic constipation” but will do so in our next analysis step and will compare it to other recent reports on comorbidity in constipation [27].

This had also consequences for the remaining and assumed functionally constipated individuals, as it challenges to label these data as representative for Germany, as we did with the data from the telephone survey [4]. However, we have gained a much better characterization and understanding of constipation, either of purely functional origin or with a putative somatic comorbidity.

However, while we may have lost the representativity of our sample of functionally constipated individuals, we have no evidence indicating that the ratio between the three subgroups (IBS-C, FC-R, and FC) has changed; neither is the sex distribution nor the age or any other descriptor any different between them. Thus we can assume that, in Germany, more than half of individuals with functional constipation do not match Rome criteria, neither for IBC-C nor for functional constipation. Whether this holds also true for the other IBS-associated symptoms, specifically diarrhea and alternating bowel habits, cannot be answered with our data, as we did not include patients reporting diarrhea in our survey, neither during telephone interviewing nor with the questionnaire. Hence, we cannot conclude either whether the ratio between IBS-subtypes that has been reported from other countries [28] is maintained in Germany.

Individuals with functional constipation (IBS-C, FC-R, and FC) appear to be similar with respect to most of the social and clinical descriptors assessed in our survey. For example, differential profile has not been observed before. The individual burden of constipation is well established [18, 19, 29, 30], as is its severity association with loss of work productivity [31] and consultation behavior [32]. When patients with IBS-C were compared to patients with FC-R and/or FC, few differences were found: non-IBS patients with painful constipation were younger, were more frequently consulters in comparison to IBS-C [6], had a higher need to strain and more incomplete evacuations [8], and had a higher age at constipation onset and higher mental health compared to IBS-C [9], and both IBS-C and FC patients with pain were significantly more bothered than patients without pain [10]. However, all four surveys did not identify specific and/or homogeneous clinical and QoL profiles as we did in our sample. In our hands, these subgroups did not differ with respect to most measures except for quality-of-life, as measured by SF-12. It appears that the major factor driving the specificity of the QoL profiles is the presence or absence of abdominal pain (Figure 1) because pain (as defined in IBC-C) lowers QoL both in the physical domain and in the emotional domain compared to other functionally constipated individuals. This is in agreement with previous reports indicating abdominal pain being the major determinant of lowered QoL in IBS [10]. When IBS-C and chronically constipated patients not matching IBS criteria were compared to patients with functional dyspepsia (FD) and gastroesophageal reflux disease (GERD) [31], those in which symptoms overlapped reported significantly higher health care utilization—an aspect we will control next in our sample.

One other characteristic of IBS-C patients is evident from our analysis of the telephone survey data (Table 3): IBS-C patients report significantly more general “gastrointestinal symptoms” than individuals with functional constipation not matching Rome criteria (FC). Whether this reflects the fact that these IBS patients suffer from abdominal pain predominantly, or whether this (also) refers to other upper and lower gastrointestinal symptoms, can unfortunately not be explored since neither the telephone survey nor the questionnaire did address such other intestinal symptoms.

Some more limitations of our data analysis need acknowledgement, beyond the self-selection biases discussed above. We also used rather liberal criteria to define “comorbid constipation” based on self-reported diagnoses and/or regular medication intake, the latter with a cut-off of 2 or more days per week. This may have inflated the number of individuals that were assembled in the group with “comorbid constipation” and downsized the number of patients with functional constipation for this analysis, since regular use of a PPI does not necessarily imply functional dyspepsia or gastric ulcer or GERD, and the frequent use of sleeping pills does not necessarily indicate a central or autonomic nervous system disturbance. In some cases, individuals reported intake of diabetic medication but not the diagnosis of diabetes, which my shed light on the comprehension of the questionnaire by some participants. Finally, the presence of a somatic disease does not necessarily indicate that constipation is caused by this disease; it may be incidental comorbidity, and the absence of a somatic condition in those labeled functional constipation does not confirm that a comorbid somatic condition does not exist; epidemiological data relying solely on subjective reports always carry the risk of false information. Therefore, some of the volunteers labeled “comorbid constipation” and excluded for this analysis may instead belong into one of the groups included in the present analysis, and such correction may diminish some of the found differences, although the opposite may happen as well.

Acknowledgments

This research was supported by a grant from Shire-Movetis NV, Belgium. The authors would like to thank Alain Joseph (Shire, Eysins, Switzerland) and Paul Hodgkins (Shire Development LLC, Wayne, Pennsylvania, USA) for their help during development of the questionnaire. They also acknowledge support by Deutsche Forschungsgemeinschaft and Open Access Publishing Fund of the University of Tübingen.

Disclosure

Johannes Leinert, Menno Smid, and Thorsten Köhler are employees of infas Institute, Bonn, Germany, and conducted the study based on a contract with the University Hospital Tübingen.

Conflict of Interests

This research was supported by a grant from Shire-Movetis NV, Belgium, to Paul Enck at the University Hospital Tübingen. Paul Enck has served as consultant in an advisory board and as speaker for Shire Germany. The authors Johannes Leinert, Menno Smid, Thorsten Köhler, and Juliane Schwille-Kiuntke declare that there is no conflict of interests regarding the publication of this paper.

Authors' Contribution

Paul Enck had the idea for the study, and Paul Enck and Juliane Schwille-Kiuntke designed the interview and questionnaire. Johannes Leinert, Menno Smid, and Thorsten Köhler contributed to interview and questionnaire design, supervised the data collection performed “in-house” at infas, conducted quality-control measures of the data, and provided the raw data (tabled, as SPSS file) for Paul Enck who evaluated the data and Paul Enck and Juliane Schwille-Kiuntke who wrote the paper.

References

  • 1.Johanson J. F., Kralstein J. Chronic constipation: a survey of the patient perspective. Alimentary Pharmacology and Therapeutics. 2007;25(5):599–608. doi: 10.1111/j.1365-2036.2006.03238.x. [DOI] [PubMed] [Google Scholar]
  • 2.Pare P., Ferrazzi S., Thompson W. G., Irvine E. J., Rance L. An epidemiological survey of constipation in Canada: definitions, rates, demographics, and predictors of health care seeking. The American Journal of Gastroenterology. 2001;96(11):3130–3137. doi: 10.1016/s0002-9270(01)03821-7. [DOI] [PubMed] [Google Scholar]
  • 3.Chu H., Zhong L., Li H., Zhang X., Zhang J., Hou X. Epidemiology characteristics of constipation for general population, pediatric population, and elderly population in China. Gastroenterology Research and Practice. 2014;2014:11. doi: 10.1155/2014/532734.532734 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 4.Enck P., Leinert J., Smid M., Köhler T., Schwille-Kiuntke J. Prevalence of constipation in the German population—a representative survey (GECCO) United European Gastroenterology Journal. 2015 doi: 10.1177/2050640615603009. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 5.Suares N. C., Ford A. C. Prevalence of, and risk factors for, chronic idiopathic constipation in the community: systematic review and meta-analysis. The American Journal of Gastroenterology. 2011;106(9):1582–1591. doi: 10.1038/ajg.2011.164. [DOI] [PubMed] [Google Scholar]
  • 6.Rey E., Balboa A., Mearin F. Chronic constipation, irritable bowel syndrome with constipation and constipation with pain/discomfort: similarities and differences. The American Journal of Gastroenterology. 2014;109(6):876–884. doi: 10.1038/ajg.2014.18. [DOI] [PubMed] [Google Scholar]
  • 7.Drossman D. A. The functional gastrointestinal disorders and the Rome III process. Gastroenterology. 2006;130(5):1377–1390. doi: 10.1053/j.gastro.2006.03.008. [DOI] [PubMed] [Google Scholar]
  • 8.Zhao Y.-F., Guo X.-J., Zhang Z.-S., et al. Epidemiology of functional diarrhea and comparison with diarrhea-predominant irritable bowel syndrome: a population-based survey in China. PLoS ONE. 2012;7(8) doi: 10.1371/journal.pone.0043749.e43749 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 9.Koloski N. A., Jones M., Young M., Talley N. J. Differentiation of functional constipation and constipation predominant irritable bowel syndrome based on Rome III criteria: a population-based study. Alimentary Pharmacology and Therapeutics. 2015;41(9):856–866. doi: 10.1111/apt.13149. [DOI] [PubMed] [Google Scholar]
  • 10.Heidelbaugh J. J., Stelwagon M., Miller S. A., Shea E. P., Chey W. D. The spectrum of constipation-predominant irritable bowel syndrome and chronic idiopathic constipation: US survey assessing symptoms, care seeking, and disease burden. The American Journal of Gastroenterology. 2015;110(4):580–587. doi: 10.1038/ajg.2015.67. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 11.Chen H., Huang X., Guo X., Peddada S. Individual and joint prevalence of three nonmotor symptoms of PD in the US general population. Movement Disorders. 2014;29(10):1316–1319. doi: 10.1002/mds.25950. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 12.Oh J.-H., Choi M.-G., Kang M.-I., et al. The prevalence of gastrointestinal symptoms in patients with non-insulin dependent diabetes mellitus. Korean Journal of Internal Medicine. 2009;24(4):309–317. doi: 10.3904/kjim.2009.24.4.309. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 13.Omair M. A., Lee P. Effect of gastrointestinal manifestations on quality of life in 87 consecutive patients with systemic sclerosis. Journal of Rheumatology. 2012;39(5):992–996. doi: 10.3899/jrheum.110826. [DOI] [PubMed] [Google Scholar]
  • 14.Triantafyllou K., Vlachogiannakos J., Ladas S. D. Gastrointestinal and liver side effects of drugs in elderly patients. Best Practice & Research: Clinical Gastroenterology. 2010;24(2):203–215. doi: 10.1016/j.bpg.2010.02.004. [DOI] [PubMed] [Google Scholar]
  • 15.Dorn S., Lembo A., Cremonini F. Opioid-induced bowel dysfunction: epidemiology, pathophysiology, diagnosis, and initial therapeutic approach. The American Journal of Gastroenterology Supplements. 2014;2(1):31–37. doi: 10.1038/ajgsup.2014.7. [DOI] [PubMed] [Google Scholar]
  • 16.Watanabe N., Omori I. M., Nakagawa A., et al. Safety reporting and adverse-event profile of mirtazapine described in randomized controlled trials in comparison with other classes of antidepressants in the acute-phase treatment of adults with depression: systematic review and meta-analysis. CNS Drugs. 2010;24(1):35–53. doi: 10.2165/11319480-000000000-00000. [DOI] [PubMed] [Google Scholar]
  • 17.Dubois D., Gilet H., Viala-Danten M., Tack J. Psychometric performance and clinical meaningfulness of the Patient Assessment of Constipation-Quality of Life questionnaire in prucalopride (RESOLOR) trials for chronic constipation. Neurogastroenterology and Motility. 2010;22(2):e54–e63. doi: 10.1111/j.1365-2982.2009.01408.x. [DOI] [PubMed] [Google Scholar]
  • 18.Nellesen D., Yee K., Chawla A., Lewis B. E., Carson R. T. A systematic review of the economic and humanistic burden of illness in irritable bowel syndrome and chronic constipation. Journal of Managed Care Pharmacy. 2013;19(9):755–764. doi: 10.18553/jmcp.2013.19.9.755. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 19.Wald A., Scarpignato C., Kamm M. A., et al. The burden of constipation on quality of life: results of a multinational survey. Alimentary Pharmacology and Therapeutics. 2007;26(2):227–236. doi: 10.1111/j.1365-2036.2007.03376.x. [DOI] [PubMed] [Google Scholar]
  • 20.Ware J. E., Jr., Kosinski M., Keller S. D. A 12-item short-form health survey: construction of scales and preliminary tests of reliability and validity. Medical Care. 1996;34(3):220–233. doi: 10.1097/00005650-199603000-00003. [DOI] [PubMed] [Google Scholar]
  • 21.American Association for Public Opinion Research. Standard Definitions: Final Dispositions of Case Codes and Outcome Rate for Survey. American Association for Public Opinion Research; 2015. https://www.aapor.org/AAPORKentico/AAPOR_Main/media/publications/Standard-Definitions2015_8theditionwithchanges_April2015_logo.pdf. [Google Scholar]
  • 22.Bender A. M., Jørgensen T., Pisinger C. Is self-selection the main driver of positive interpretations of general health checks? The Inter99 randomized trial. Preventive Medicine. 2015;81:42–48. doi: 10.1016/j.ypmed.2015.07.004. [DOI] [PubMed] [Google Scholar]
  • 23.van der Waal D., Broeders M. J., Verbeek A. L., Duffy S. W., Moss S. M. Case-control studies on the effectiveness of breast cancer screening: insights from the UK age trial. Epidemiology. 2015;26(4):590–596. doi: 10.1097/EDE.0000000000000285. [DOI] [PubMed] [Google Scholar]
  • 24.Wallander L., Tikkanen R. H., Mannheimer L. N., Östergren P.-O., Plantin L. The problem of non-response in population surveys on the topic of HIV and sexuality: a comparative study. European Journal of Public Health. 2014;25(1):172–177. doi: 10.1093/eurpub/cku154. [DOI] [PubMed] [Google Scholar]
  • 25.Khazaal Y., van Singer M., Chatton A., et al. Does self-selection affect samples' representativeness in online surveys? An investigation in online video game research. Journal of Medical Internet Research. 2014;16(7, article e164) doi: 10.2196/jmir.2759. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 26.Spix C., Berthold F., Hero B., Michaelis J., Schilling F. H. Correction factors for self-selection when evaluating screening programmes. Journal of Medical Screening. 2015 doi: 10.1177/0969141315597959. [DOI] [PubMed] [Google Scholar]
  • 27.Choung R. S., Rey E., Locke G. R., III, et al. Chronic constipation and co-morbidities: a prospective population-based nested case-control study. United European Gastroenterology Journal. 2014 doi: 10.1177/2050640614558476. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 28.Hungin A. P. S., Whorwell P. J., Tack J., Mearin F. The prevalence, patterns and impact of irritable bowel syndrome: an international survey of 40,000 subjects. Alimentary Pharmacology and Therapeutics. 2003;17(5):643–650. doi: 10.1046/j.1365-2036.2003.01456.x. [DOI] [PubMed] [Google Scholar]
  • 29.Wald A., Sigurdsson L. Quality of life in children and adults with constipation. Best Practice & Research: Clinical Gastroenterology. 2011;25(1):19–27. doi: 10.1016/j.bpg.2010.12.004. [DOI] [PubMed] [Google Scholar]
  • 30.Koloski N. A., Jones M., Wai R., Gill R. S., Byles J., Talley N. J. Impact of persistent constipation on health-related quality of life and mortality in older community-dwelling women. The American Journal of Gastroenterology. 2013;108(7):1152–1158. doi: 10.1038/ajg.2013.137. [DOI] [PubMed] [Google Scholar]
  • 31.Neri L., Basilisco G., Corazziari E., et al. Constipation severity is associated with productivity losses and healthcare utilization in patients with chronic constipation. United European Gastroenterology Journal. 2014;2(2):138–147. doi: 10.1177/2050640614528175. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 32.Vakil N., Stelwagon M., Shea E. P., Miller S. Symptom burden and consulting behavior in patients with overlapping functional disorders in the US population. United European Gastroenterology Journal. 2015 doi: 10.1177/2050640615600114. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Gastroenterology Research and Practice are provided here courtesy of Wiley

RESOURCES