Background
Inflammatory bowel disease (IBD), including Crohn`s disease (CD) and ulcerative colitis (UC), is characterized by chronic, recurrent inflammation of the gastrointestinal tract. In UC, inflammation is located in the colonic mucosa and varies in extent. However, in CD, inflammation may affect the entire gastro-intestinal tract, from the mouth to the anus. The pathogenesis of IBD is not completely understood but is commonly regarded as a dysregulation of the immune response against the intestinal microbiota in genetically susceptible individuals [1]. The course of IBD may be unpredictable, ranging from mild symptoms with rare relapses to serious intestinal inflammation, requiring long-term immunosuppressive medical treatment, hospitalization, and, in some cases, surgery [2].
Symptoms associated with IBD are predominantly diarrhea with or without mucus and blood, as well as abdominal pain, tenesmus, rectal urgency, rectal bleeding, weight loss, anorexia, and fever [3, 4]. Furthermore, fatigue, anxiety, sleep impairment, psychological distress, and depression are commonly reported in patients with IBD [5‐8]. Even though symptoms are more common during periods of active disease, they can also occur and persist when patients are in remission [7, 9‐11]. A symptom can be defined as “a manifestation of disease apparent to the patient himself, while a sign is a manifestation of disease that the physician perceives” [12]. In IBD, symptom research has gained increased attention in the last decades, and studies have also shown a discrepancy between how patients and physicians view the impact of IBD on daily life [13].
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In order to understand the relationship between symptoms as well as their potential combined impact on patient outcomes, the concept of symptom clusters has been introduced and investigated in several medical conditions, including cancer, cardiovascular disease, kidney disease, human immunodeficiency virus infection, and chronic obstructive pulmonary disease [14‐18]. Symptom clusters, defined by Kim et al. [14] as “two or more symptoms that are related to each other and that occur together,” [14] are particularly relevant in IBD since patients seldom present with just one single symptom [11, 19]. Symptom clusters are furthermore defined as “stable groups of symptoms are relatively independent of other clusters, and may reveal specific underlying dimensions of symptoms” [14].
To our knowledge, only one cohort study [20] and one retrospective study [21] have investigated symptom clusters in IBD. Perler et al. investigated disease-specific symptoms in patients prior to diagnosis, [20] and Conley et al. investigated physical, as well as psychological symptoms, in patients with long disease durations [21]. As the available research on IBD is limited, [20, 21] there is a need for improved understanding of symptoms and symptom clusters as well as their association with clinical and demographic factors. This knowledge may potentially guide future symptom management strategies.
Thus, the primary aim of this study was to estimate the prevalence of symptoms as well as the occurrence of symptom clusters in a population-based cohort of patients newly diagnosed with IBD. Moreover, the study aimed to assess potential associations between specific clusters and socio-demographic and clinical factors.
Methods
Study design, population, and data collection
The Inflammatory Bowel Disease in South-Eastern Norway III (IBSEN III) study is a prospective population-based inception cohort that included all new cases of IBD and symptomatic non-IBD controls from a well-defined geographical area in the south-eastern part of Norway (catchment area of 2.95 million inhabitants in 2017) from 2017 to 2019. All patients with symptoms and clinical findings suspicious of IBD were referred to their local hospital by general practitioners and private gastroenterology centres in the South-East Health Region. Standardized clinical, biochemical, endoscopic and demographic data were collected and analysed at baseline in line with the study`s standard operating procedure. Analyses of routine blood samples were performed at the local laboratories as a part of the routine follow-up. Calprotectin analyses were performed at the same laboratory for all patients. Further details on study design and patient inclusion are described elsewhere [22]. The diagnosis of CD and UC was based on the Lennard-Jones criteria [23]. Patients were excluded if they had no histopathological or radiological findings of CD or UC or were diagnosed with bowel inflammation due to other causes. At the three largest hospitals in the research catchment area (Oslo University Hospital, Akershus University Hospital, and Vestfold Hospital Trust), adult patients (age, ≥ 18 years) were asked to complete an extensive set of patients’ reported outcome measures (PROMs), as described below.
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Clinical and sociodemographic data
At the time of diagnosis, all patients underwent colonoscopies with biopsies. Fecal samples for the analysis of calprotectin as a biomarker of disease activity and blood samples were collected. Clinical disease activity was assessed using the Harvey Bradshaw Index (HBI) for CD [24] and the Simple Clinical Colitis Activity Index (SCCAI) for UC [25]. An HBI score ≤ 4 and SCCAI score < 2.5 were used as cut-off values for inactive disease in CD and UC, respectively [26]. Fecal calprotectin values of < 250 and ≥ 250 µg/g were defined as remission and active inflammation, respectively [27‐29]. Hemoglobin (Hgb) levels of < 12 g/dl for females and < 13 g/dl for men were defined as anemia, [30] and a 25(OH) vitamin D value of < 50 nmol/L was defined as deficiency [31]. Ferritin values of < 30 and < 100 µg/L were defined as indicative of iron deficiency in patients with calprotectin levels of < 250 and ≥ 250 µg/g, respectively [30]. Fecal calprotectin was chosen as an indicator of disease activity as it has been shown to be a superior biomarker compared with CRP and leucocytes [32]. Sociodemographic data were self-reported and included age, gender, marital status, level of education, and current smoking and work status. Marital status was dichotomized into living together (married/co-inhabitant) or living alone (single/widow(er), separated/divorced). Educational status was dichotomized into higher education (> 12 years, upper secondary school, college, or university) and basic education only (≤ 12 years). Work status was dichotomized into work-related activity (employed/student) and no work-related activity (homemaker, disability beneficiary, unemployed, or retired).
Memorial symptom assessment scale (MSAS)
To investigate symptoms and potential symptom clusters in IBD, the Memorial Symptom Assessment Scale (MSAS) questionnaire was used. Portenoy et al. developed the original MSAS to provide information about a diverse group of common symptoms among patients with malignant diseases [33]. The questionnaire contains 32 physical and psychological symptoms, asking patients to report the presence or absence on these symptoms during the past week. The MSAS has been psychometrically tested and found to be a reliable, valid, and comprehensive instrument for the assessment of symptom prevalence, characteristics, and distress [33]. The questionnaire has been translated into Norwegian [34] but has not been specifically validated in a population with IBD. MSAS was administered electronically to the patients using an internet-based system for patient-reported outcome measures (ViedocMe).
Statistical analyses
Continuous data are presented as median and range for variables with skewed distribution and mean and standard deviation for normally distributed data. Categorical variables are presented as counts and percentages. Group comparisons were performed using independent t-tests for normally distributed data, chi-square tests for categorical data, or Mann–Whitney U-tests for non-normally distributed continuous data.
We assessed the symptom prevalence in CD and UC separately (Supplementary Table 1), and the most prevalent symptoms in the two diagnostic groups were comparable. We therefore concluded that analyzing IBD collectively was an acceptable solution in this study to investigate symptom clusters. To investigate the presence of possible symptom clusters, we used exploratory principal component analysis (PCA). This technique allows a large number of variables to be reduced or summarized into smaller components, called clusters, while keeping most of the variation intact: it identifies groupings of variables and examines the relationship between variables [35]. PCA was executed using the symptoms experienced by ≥ 50% of the included patients. Seventeen out of 350 patients had missing data on the MSAS and were consequently excluded from the cluster analysis. An eigenvalue > 1 was used to extract clusters, and, in addition, scree plots were inspected. The factor loading threshold was set at 0.4 in accordance with recommendations in the literature [36]. When interpreting the results, a symptom could only load on one cluster and the highest factor loading determined which cluster each evaluated symptom belonged to. We chose the number of extracted clusters to be three as this solution explained the highest amount of the total variance, and the extracted clusters were formed with variables that could be interpreted in a clinically meaningful way.
Multinominal logistic regression was performed to assess the relationship between symptom cluster membership as described above (i.e., dependent variable) and selected sociodemographic and clinical variables. Variables with an association with the cluster membership with a p-value < 0.20 in univariate analyses were included in a multinomial regression model, together with gender and age. Backwards selection was performed to evaluate the strength of the association between the independent variables and cluster membership. Effect estimates were presented as odds ratios (ORs) with 95% confidence intervals (CIs). To improve precision, we used bootstrapping with 10,000 repetitions and bias correction to derive CIs. All analyses were considered exploratory; thus, no correction for multiple testing was performed. All tests were two-sided, and p-values ≤ 0.05 were considered statistically significant. All data were analyzed using IBM SPSS, version 28 (IBM Corp., Armonk, NY, USA).
Results
Study population
Of the 573 patients (age, ≥ 18 years) with a verified diagnosis of UC or CD, 350 completed the MSAS questionnaire (61.1%) (Fig. 1). When comparing those who answered the MSAS questionnaire (responders) with those who did not (non-responders), the groups were comparable with regards to gender, age, education and disease activity, except for smoking, which was significantly more prevalent among the non-responders (14% vs. 7.4%, p = 0.03). Patient characteristics are presented in Table 1.
Fig. 1
Patient enrollment flowchart
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Table 1
Characteristics of patients newly diagnosed with inflammatory bowel disease (N = 350)
IBD | CD | UC | |
|---|---|---|---|
N = 350
|
n = 119
|
n = 231
| |
Sociodemographic characteristics
| |||
Age (mean, SD) | 39.0 (14.4) | 40.1 (15.4) | 38.5 (13.9) |
Gender, n (%) | |||
Female | 174 (49.7) | 68 (57.1) | 106 (45.9) |
Male | 176 (50.3) | 51 (42.9) | 125 (54.1) |
Education, n (%) | |||
University; ≥2 years | 177 (50.6) | 57 (47.9) | 120 (51.9) |
Elementary/upper secondary | 173 (49.4) | 62 (52.1) | 111 (48.1) |
Marital status, n (%) | |||
Married/co-inhabitant | 236 (67.4) | 75 (63.0) | 161 (69.7) |
Single/widow(ed) | 114 (32.6) | 44 (37.0) | 70 (30.3) |
Work status, n (%) | |||
Working | 297 (84.9) | 96 (80.7) | 201 (87.0) |
Not working | 53 (15.1) | 23 (19.3) | 30 (13.0) |
Clinical characteristics
| |||
Diagnosis, n (%) | |||
Crohn’s disease | 119 (34.0) | ||
Ulcerative colitis | 231 (66.0) | ||
Montreal - location for CD, n (%) | |||
Ileal (L1) | 61 (51.3) | ||
Colonic (L2) | 24 (20.2) | ||
Ileocolonic (L3) | 34 (28.6) | ||
Upper tract only or modifier (L4)a
| 2 (1.7) | ||
Montreal – behavior for CD, n (%) | |||
Non-stricturing, non-penetrating (B1) | 92 (77.3) | ||
Stricturing (B2) | 25 (21.0) | ||
Penetrating (B3) | 2 (1.7) | ||
Perianal disease (B4)a
| 10 (8.4) | ||
Montreal – extent for UC, n (%) | |||
Ulcerative proctitis (E1) | 94 (40.7) | ||
Left-sided UC (E2) | 53 (22.9) | ||
Extensive UC (E3) | 84 (36.4) | ||
Montreal disease severity for UC, n (%) | |||
Clinical remission (S0) | 4 (1.7) | ||
Mild UC (S1) | 92 (39.8) | ||
Moderate UC (S2) | 115 (49.8) | ||
Severe UC (S3) | 20 (8.7) | ||
Calprotectin ≥ 250 µg/g | 158 (52.0) | 56 (54.4) | 102 (50.7) |
Missing, n (%)
|
46 (13.1)
| ||
Elevated HBI/SCCAIb, n (%) | 190 (55.6) | 56 (48.3) | 134 (59.3) |
Missing, n (%)
|
8 (2.3)
| ||
25-OH Vitamin D deficiencyc, n (%)
| 98 (28.2) | 29 (24.6) | 69 (30.1) |
Missing, n (%)
| 3 (0.9) | ||
Anemiad, n (%) | 45 (12.9) | 16 (13.4) | 29 (12.7) |
Missing, n (%)
| 2 (0.6) | ||
Iron deficiencye, n (%)
| 104 (34.4) | 30 (29.4) | 74 (37.0) |
Missing, n (%)
| 48 (13.8) | ||
Current tobacco use, n (%) | 26 (7.4) | 13 (10.9) | 13 (5.6) |
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Symptom prevalence
The prevalence of each of the 32 MSAS symptoms is listed in Fig. 2. The 11 most prevalent symptoms reported by at least half of the patients with IBD were feeling bloated (83%), feeling drowsy (81%), lack of energy (81%), pain (75%), worrying (71%), diarrhea (65%), feeling irritable (66%), difficulty sleeping (58%), feeling sad (55%), difficulty concentrating (53%), and feeling nervous (51%). We also assessed the prevalence in CD and UC separately (Supplementary Table 1), and these 11 most prevalent symptoms were present in both groups.
Fig. 2
Prevalence of self-reported symptoms in patients newly diagnosed with IBD. *Other < 30%: itching, cough, numbness and tingling in hands and feet, shortness of breath, changes in skin, mouth sores, hair loss, ”don’t look like myself,” problems with urination, change in the way food tastes, swelling of arms or legs, difficulty swallowing, or vomiting
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When data were categorized according to clinical disease activity status (Table 2), a significantly higher proportion of patients with active disease, compared with those with inactive disease, reported lack of energy (87.2%, 95% CI [81.5–91.6] vs. (73.2%, 95% CI [65.3–80.1]), diarrhea (77.2%, 95% CI [70.6–83.0] vs. (50.3%, 95% CI [42.1–58.6]), problems with sexual interest/activity (53.5%, 95% CI [46.1–60.8] vs. (31.3%, 95% CI [24.0-39.4]), and dizziness (53.2%, 95% CI [45.8–60.5] vs. (34.7%, 95% CI [27.1–42.9]).
Table 2
Prevalence of symptoms in patients newly diagnosed with inflammatory bowel disease specified by clinical disease activity statusa
Symptom | Active disease (n = 190) | Inactive disease (n = 152) | ||||||
|---|---|---|---|---|---|---|---|---|
n | missing | % | 95% CI | n | missing | % | 95% CI | |
Feeling bloated | 164 | 3 | 87.7 | 82.1–92.0 | 118 | 1 | 78.1 | 71.0-84.5 |
Lack of energy | 163 | 3 |
87.2
|
81.5–91.6
| 109 | 3 |
73.2
|
65.3–80.1
|
Feeling drowsy | 157 | 2 | 83.5 | 77.4–88.5 | 116 | 3 | 77.9 | 70.3–84.2 |
Pain | 149 | 1 | 78.8 | 72.3–84.4 | 101 | 4 | 68.2 | 60.1–75.6 |
Diarrhea | 146 | 1 |
77.2
|
70.6–83.0
| 76 | 1 |
50.3
|
42.1–58.6
|
Worrying | 140 | 1 | 74.1 | 67.2–80.2 | 98 | 3 | 64.8 | 57.6–73.3 |
Feeling irritable | 124 | 2 | 66.0 | 58.7–72.7 | 85 | 3 | 57.0 | 48.7–65.1 |
Difficulty sleeping | 119 | 3 | 63.6 | 56.3–70.5 | 74 | 5 | 50.3 | 42.0-58.7 |
Feeling sad | 113 | 1 | 59.8 | 52.4–66.8 | 72 | 3 | 48.3 | 40.1–56.6 |
Difficulty concentrating | 109 | 2 | 58.0 | 50.6–65.1 | 68 | 2 | 45.3 | 37.2–53.7 |
Problems with sexual interest/activity | 100 | 3 |
53.5
|
46.1–60.8
| 47 | 2 |
31.3
|
24.0-39.4
|
Feeling nervous | 101 | 1 | 53.4 | 46.1–60.7 | 72 | 3 | 48.3 | 40.1–56.6 |
Dizziness | 100 | 2 |
53.2
|
45.8–60.5
| 52 | 2 |
34.7
|
27.1–42.9
|
Nausea | 85 | 2 | 45.2 | 38.0-52.6 | 50 | 2 | 33.3 | 25.9–41.5 |
Lack of appetite | 81 | 2 | 43.1 | 36.0-50.5 | 44 | 2 | 29.3 | 22.2–37.3 |
Sweats | 73 | 2 | 38.8 | 31.8–46.2 | 53 | 2 | 35.3 | 27.7–43.5 |
Dry mouth | 71 | 3 | 38.0 | 31.0-45.3 | 46 | 5 | 31.3 | 24.0-39.5 |
Weight loss | 67 | 2 | 35.6 | 28.8–43.0 | 36 | 2 | 24.0 | 17.4–31.6 |
Constipation | 66 | 3 | 35.3 | 28.5–42.6 | 47 | 2 | 31.3 | 24.0-39.4 |
Cough | 54 | 1 | 28.6 | 22.2–35.6 | 34 | 6 | 23.3 | 16.7–31.0 |
Itching | 50 | 2 | 26.6 | 20.4–33.5 | 38 | 2 | 25.3 | 18.6–33.1 |
Shortness of breath | 50 | 2 | 26.6 | 20.4–33.5 | 27 | 2 | 18.0 | 12.2–25.1 |
Numbness and tingling in hands and feet | 47 | 3 | 25.1 | 19.1–32.0 | 40 | 3 | 26.8 | 20.0-34.7 |
Mouth sores | 43 | 5 | 23.2 | 17.4–30.0 | 23 | 2 | 15.3 | 10.0-22.1 |
Changes in skin | 43 | 1 | 22.8 | 17.0-29.4 | 28 | 3 | 18.8 | 12.9–26.0 |
Problems with urination | 38 | 1 | 20.1 | 14.6–26.5 | 14 | 3 | 9.4 | 5.2–15.3 |
Change in the way food tastes | 36 | 2 | 19.1 | 13.8–25.5 | 15 | 2 | 10.0 | 5.7–16.0 |
Hair loss | 36 | 1 | 19.0 | 13.7–25.4 | 24 | 2 | 16.0 | 11.0-22.9 |
“I don`t look like myself” | 35 | 1 | 18.5 | 13.3–24.8 | 23 | 1 | 15.2 | 10.0–22.0 |
Swelling of arms or legs | 31 | 2 | 16.5 | 11.5–22.6 | 13 | 3 | 8.7 | 4.7–14.5 |
Vomiting | 22 | 1 | 11.6 | 7.4–17.1 | 6 | 4 | 4.1 | 1.5–8.6 |
Difficulty swallowing | 21 | 2 | 11.2 | 7.0-16.6 | 9 | 2 | 6.0 | 2.3–11.1 |
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Symptom clusters
Three symptom clusters with factor loadings > 0.6 explaining 54% of the total variance were identified (Table 3). Cluster I, labelled as the psychological cluster, included 55.6% of the patients and consisted of five symptoms: feeling worried, feeling sad, feeling nervous, feeling irritable, and having difficulty concentrating. Cluster II, labelled as the impaired energy cluster, included 28.2% of the patients and consisted of three symptoms: lack of energy, feeling drowsy, and difficulty sleeping. Cluster III, labelled as the physical cluster, included 16.2% of the patients and consisted of three symptoms: diarrhea, feeling bloated, and pain.
Table 3
Principal components analysis of symptom clustering in patients with inflammatory bowel disease
Cluster I (Psychological) | Cluster II (Impaired energy) | Cluster III (Physical) | |
|---|---|---|---|
Worrying |
0.84
| 0.29 | 0.19 |
Feeling sad |
0.82
| 0.34 | 0.17 |
Feeling nervous |
0.81
| 0.26 | 0.28 |
Feeling irritable |
0.64
| 0.53 | 0.23 |
Difficulty concentrating |
0.64
| 0.53 | 0.13 |
Lack of energy | 0.34 |
0.82
| 0.26 |
Feeling drowsy | 0.32 |
0.81
| 0.15 |
Difficulty sleeping | 0.37 |
0.60
| 0.32 |
Diarrhea | 0.19 | 0.10 |
0.79
|
Feeling bloated | 0.20 | 0.28 |
0.65
|
Pain | 0.26 | 0.57 |
0.62
|
Factors associated with symptom cluster membership
In the multinomial logistic regression analysis, Cluster III (physical cluster) was set as the reference cluster. Cluster III was chosen as a reference since it was distinctly different from the other clusters with regards to cluster item content (i.e., physical symptoms).
The results of the univariate and multinomial analyses are presented in Table 4. In the univariate analyses, there were no statistically significant associations between the selected possible predictive factors and cluster membership. In the multinomial analysis, however, vitamin D deficiency was associated with an increased odds (OR 2.49, 95% CI [1.00-6.20] p = 0.05) of being in Cluster II (impaired energy) vs. Cluster III (physical cluster). No statistically significant associations were found between clinical disease activity status, fecal calprotectin ≤ 250 µg/g, level of education, age, gender, and cluster membership.
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Table 4
Variables associated with symptom cluster membership: results from univariate and multinomial regression analyses
Psychological cluster vs. physical cluster | Impaired energy cluster vs. physical cluster | ||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Univariate | Multinomial | Univariate | Multinomial | ||||||||||
Variable | OR | 95% CI |
p-value | OR | 95% CI |
p-value | OR | 95% CI |
p-value | OR | 95% CI |
p-value | |
Gender | |||||||||||||
Male (ref) | 1 | 1 | |||||||||||
Female | 0.75 | 0.41–1.38 | 0.35 | 0.91 | 0.46–1.81 | 0.79 | 1.07 | 0.55–2.09 | 0.85 | 1.22 | 0.57–2.61 | 0.62 | |
Age | 1.0 | 0.98–1.02 | 0.89 | 0.99 | 0.97–1.02 | 0.63 | 1.00 | 0.98–1.02 | 0.98 | 0.99 | 0.96–1.02 | 0.38 | |
Diagnosis | |||||||||||||
UC (ref) | 1 | 1 | |||||||||||
CD | 0.81 | 0.42–1.55 | 0.52 | - | 1.14 | 0.55–2.36 | 0.72 | - | |||||
Marital status | |||||||||||||
Married/co-habitant (ref) | 1 | 1 | |||||||||||
Single/widowed | 1.22 | 0.64–2.31 | 0.54 | - | 1.00 | 0.50–2.02 | 0.99 | - | |||||
Education level | |||||||||||||
>12 years (ref) | 1 | 1 | |||||||||||
<12 years | 0.93 | 0.51–1.70 | 0.81 | - | 1.61 | 0.82–3.17 | 0.17 | 1.57 | 0.74–3.35 | 0.24 | |||
Work status | |||||||||||||
Working (ref) | 1 | 1 | |||||||||||
Not working | 0.65 | 0.25–1.64 | 0.36 | - | 0.78 | 0.28–2.18 | 0.64 | - | |||||
Calprotectin | |||||||||||||
< 250 µg/g (ref) | 1 | 1 | |||||||||||
≥ 250 µg/g | 1.76 | 0.89–3.48 | 0.10 | 1.80 | 0.88–3.69 | 0.11 | 2.07 | 0.98–4.36 | 0.06 | 1.69 | 0.76–3.75 | 0.20 | |
HBI/SCCAI* | |||||||||||||
Remission (ref) | 1 | 1 | |||||||||||
Disease activity | 1.38 | 0.73–2.59 | 0.32 | - | 1.84 | 0.92–3.68 | 0.08 | 1.46 | 0.66–3.21 | 0.35 | |||
25(OH) vitamin D** | |||||||||||||
Normal(ref) | 1 | 1 | |||||||||||
Deficiency | 1.11 | 0.58–2.13 | 0.74 | - | - | 2.06 | 0.96–4.42 | 0.07 |
2.49
|
1.00-6.20
|
0.05
| ||
Ferritin*** | |||||||||||||
Normal (ref) | 1 | 1 | |||||||||||
Iron deficiency | 0.85 | 0.42–1.71 | 0.65 | - | 0.87 | 0.43–1.87 | 0.72 |
-
| |||||
Hemoglobin*** | |||||||||||||
Normal (ref) | 1 | 1 | |||||||||||
Anemia | 1.09 | 0.46–2.57 | 0.85 | - | 1.47 | 0.54-4.00 | 0.45 |
-
| |||||
Discussion
This was a population-based cohort study of patients newly diagnosed with IBD. Feeling drowsy, feeling bloated, and lack of energy were identified as the three most frequently occurring symptoms, regardless of clinical disease activity status. Furthermore, three distinct symptom clusters were identified: psychological, impaired energy, and physical clusters. Except for vitamin D deficiency, which was associated with the impaired energy cluster, no other factor was associated with cluster membership.
The most prevalent symptoms observed in the current study are in line with prior findings in IBD research [11, 37]. However, the prevalence of the individual symptoms was higher than those previously reported. There may be several explanations for these differences, including differences in disease duration. While we included newly diagnosed patients, the patients in a study by Farrell et al. [11] had a median disease duration of 10 years, and those in a study by Singh et al. [37] had a disease duration of 22 years. Having received medical and surgical treatments as well as time to adjust to a life with a chronic disease may potentially help explain the higher symptom prevalence in our study compared with that in previous studies. Even though the prevalence of the individual symptoms seems to be higher at the time of diagnosis, findings across studies indicate that the type of symptoms experienced by patients with IBD seems to be consistent.
In line with previous research [7, 9‐11, 37], we observed a higher symptom prevalence in active disease than that in inactive disease. The finding that dizziness is a more prevalent symptom in patients with active disease is of interest. However, it is difficult to draw clear conclusions based on this finding. One potential hypothesis may be that increased dizziness is associated with loss of blood, electrolytes, vitamins, and minerals commonly seen in active disease. However, in our study, in the patients with active disease, 25-OH Vitamin D deficiency, iron deficiency and anaemia were comparable between those reporting dizziness and those not reporting dizziness.
Interestingly, lack of energy was experienced by more than 70% of patients with clinically inactive disease. Furthermore, the five symptoms feeling bloated, feeling drowsy, lack of energy, pain, and worrying were reported by more than 60% of the patients with inactive disease, which highlights the high symptom prevalence experienced by these patients.
Psychological symptoms (i.e., worrying, feeling sad, feeling irritable, and feeling nervous) were among the most prevalent symptoms in our study, and they were more prevalent than reported by Farrell et al. [11]. Our findings highlight the psychological challenges patients experienced and may underline the importance of addressing disease coping and providing psychological support at the time of diagnosis. A qualitative study of IBD patient experiences described that living with IBD had a huge impact on mental health, causing stress, anxiety, and uncertainty about the future [38]. Indeed, it is well known that patients with IBD express the need for psychological follow-up and support [38‐41].
We identified three distinct symptom clusters, i.e., psychological, impaired energy, and physical clusters, in the present study. Two earlier studies investigated symptom clusters in IBD [20, 21]. However, a cross-comparison of the studies is difficult due to different study designs, analyses, and patient cohorts. In the retrospective study by Conley et al., [21] patients had a mean disease duration of 14.4 years, and clusters were identified based on questionnaires different from those used in the current study. Furthermore, the authors performed different statistical analyses and latent class analysis (LCA), and they identified four symptom clusters categorized as follows: physical, psychological, low symptom burden, and high symptom burden clusters [21]. In line with this current study, the study by Perler et al. [20] included patients at the time of diagnosis, but another questionnaire rather than the MSAS questionnaire was used to assess symptoms. Perler et al. identified three identical symptom clusters for UC and CD. These clusters were labelled “bowel frequency and abdominal discomfort,” “systemic/extraintestinal symptoms,” and “anorectal symptoms.” In addition, two clusters were identified that were specific to each diagnosis, namely “upper abdominal symptoms” in patients with CD and “incontinence and flatus” in UC [20]. As for statistical analyses, PCAs were used to cluster symptoms in both the study by Perler et al. [20] and the current study.
The cluster comprising psychological symptoms (i.e., worrying, feeling sad, nervous, irritable, and difficulties concentrating) included more than half of the patients in this study. Being diagnosed with a chronic disease like IBD may constitute an existential challenge, causing uncertainty and stress, as well as the need to adapt and develop coping strategies [4]. The first months after diagnosis can be challenging for patients, facing the complexity of medical information [39]. Schoefs et al. [42] found that the patient’s mental well-being was greatly affected by an IBD diagnosis, and the need for psychological and mental help and guidance to cope with the disease were warranted. Furthermore, patients expressed that little attention was given to the mental aspects of the disease [42]. The identification of a psychological cluster is not surprising, at least when comparing with symptom cluster research in other fields, such as oncology. A recent systematic review in cancer research found that psychological clusters were the most common clusters, identified in 82.6% of the included studies [43].
The impaired energy cluster included the symptoms of lack of energy, feeling drowsy, and difficulty sleeping. While the impaired energy cluster does not specifically measure fatigue, it is well known that reduced energy/fatigue is frequently reported in IBD [42, 44, 45] and has been described by patients as a feeling of “lack of energy” and “a constant state of exhaustion” [40]. Moreover, lack of energy is one of the main concerns among patients with IBD [46‐48] and one of their most burdensome symptoms [11]. Sleep impairment, poor sleep quality, altered sleep patterns, and fragmentation of sleep are common in patients with IBD [45, 49‐51]. Furthermore, a prior study demonstrated that sleep disturbance may be linked to the perception of fatigue [50].
The physical cluster included the symptoms of diarrhea, feeling bloated, and pain, all known symptoms of IBD [3]. However, only 16% of the patients belonged to the physical cluster. Despite MSAS having been widely used and allowing cross-comparison, using such a generic assessment tool may potentially limit the identification of disease-specific symptoms in IBD.
Vitamin D deficiency was statistically significantly associated with the impaired energy cluster. Vitamin D deficiency is more prevalent in patients with IBD than in the general population [52]. This deficiency is associated with malabsorption, reduced sunlight exposure, insufficient physical activity, and reduced vitamin D intake [53, 54]. A meta-analysis found that a low vitamin D status was a marker for lower quality of life scores [55] and was associated with muscle weakness and increased disease activity in patients with IBD [31, 53, 54]. Even though the association between vitamin D deficiency and fatigue has been studied in IBD, no certain associations have been established [56]. Hence, our finding is of interest and warrants further exploration. As none of the other clinical or socio-demographic variables were associated with cluster membership, this warrants an individual patient approach by health-care professionals.
Strength and limitations
The strength of this study is the use of data from a large population-based inception cohort of patients newly diagnosed with IBD (IBSEN III), including rigorous data collection, handling, and monitoring. Nonetheless, this study has some limitations. First, the MSAS questionnaire response rate was low (350 of 573 [61.1%] patients answered the MSAS questionnaire), reducing the study sample. However, the non-responders and responders were comparable regarding gender, age, level of education and disease activity, thus we consider the sample of responders to be still representative for the IBD population originally sampled from. Second, even though the 333 patients in this study were enough to perform cluster analysis, the number of patients in each diagnostic group was very limited, hampering our ability to explore symptom clusters in CD and UC separately. However, we assessed the prevalence in CD and UC separately, and the most prevalent symptoms in the two diagnostic groups were comparable; therefore, we concluded that analyzing IBD collectively was an acceptable solution in this study. Third, the MSAS questionnaire was electronically administered for self-reporting of symptoms, and it is unknown whether reporting digitally had an impact on the response rate in this study. Nevertheless, a recent systematic review found a clear patient preference, acceptability, higher data quality, and response rates when digital questionnaires were administered instead of paper questionnaires [57]. Fourth, we do not have data to assess and control for potential psychiatric conditions, which might have given us a more in-depth characterization of the study population. Finally, the MSAS was originally developed and validated for oncology patient populations and used in diseases such as cancer, AIDS, and in patients with advanced medical illnesses [33, 58]. Since the MSAS has not been validated in an IBD population, it is possible that it may not be sensitive enough to specific symptoms that patients with IBD experience.
Conclusions
This study confirms the high symptom prevalence experienced by patients with IBD at the time of diagnosis. Even though three distinct symptom clusters were identified and the role of vitamin D deficiency on lack of energy warrant further exploration, our data did not reveal any associations between symptom clusters and socio-demographic and clinical data. The identification of the three symptom clusters may be useful knowledge in evidence-based decision-making and patient management, as the patients’ needs, and follow-up may differ among the clusters. Our findings point to the need to recognize and address multiple symptoms in IBD, select relevant interventions that target single and multiple symptoms, and to evaluate the outcomes. The large proportion of patients in the psychological cluster underlines the need for individualized psychosocial support at the time of diagnosis to prevent health challenges in a long-term perspective for patients with IBD. Furthermore, large longitudinal studies that examine trajectories of symptom clusters are needed to provide results that are more definitive and will potentially clarify the impact these symptom clusters might have on health and functioning, thereby informing targeted intervention efforts.
Acknowledgements
We thank all patients participating in the IBSEN III study and the health care professionals at the inclusion sites for the inclusion and follow-up of patients. We would also like to thank Editage (www.editage.com) for English language editing.
Declarations
Ethics approval and consent to participate
The IBSEN III study (Clinical Trials ID: NCT02727959, first trial registration date 05/04/2016) was approved by the South-East Regional Committee for Medical and Health Research Ethics (Ref. 2015/946-3), and all patients signed written informed consent forms before participating in the study. The study was performed in accordance with the ethical guidelines of the Declaration of Helsinki.
Consent for publication
Not applicable.
Competing interests
IJ, MCS, SL, CL, BO, GHH, TA, M-BB, PR, L-PJJ, and RO declare no competing interest. VAK received speaker fees from Janssen-Cilag AS, consultant fees and scientific board fees from Takeda AS, and advisory board fees from Tillotts Pharma AG. MLH received speaker fees from Galapagos, Ferring, BMS, Janssen, AbbVie, Meda, Tillotts, and Takeda; is on the advisory boards of Takeda, Galapagos, BMS, and AbbVie; and initiated research grants from Takeda, Pfizer, Tillotts, and Ferring. VS received grants from Takeda AS. TED has served as a speaker, consultant, or advisory board member for AbbVie, Ferring, Pfizer, Pharmacosmos, Tillotts, and Vifor Pharma. Furthermore, he has received ounrestricted research grants from AbbVie and Pharmacosmos. SOF received personal fees from Takeda, Galapagos, Jansen-Cilag, AbbVie, Pharmacosmos, Norgine, and Bristol-Myers-Squibb outside the submitted work.
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