Skip to main content
Clinics and Practice logoLink to Clinics and Practice
. 2026 Feb 24;16(3):45. doi: 10.3390/clinpract16030045

Characteristics, Complications, Comorbidities, and Other Manifestations of Inflammatory Bowel Disease: A 7-Year Tertiary Center Experience

Waleed Alharbi 1,2,*, Turki Alasmari 1,2, Najla Al Rasheed 2,3, Jamila A Alonazi 2,3, Naif K Alaqil 1,2,*, Meshari Al Samih 1,2, Nawaf S Alzahrani 1,2, Abdulaziz Bin Akrish 2,3, Soliman Alaraidh 3,4
Editors: Athanassios A Kyrgidis, Anna Capasso
PMCID: PMC13024980  PMID: 41892489

Abstract

Background/Objectives: Inflammatory bowel disease (IBD) is associated with significant morbidity worldwide. While global epidemiological trends are well-documented, data on the clinical and demographic characteristics of IBD patients in Saudi Arabia remain limited. This study aimed to evaluate the distribution of multimorbidity among IBD patients in a tertiary Saudi hospital and assess associated clinical features and outcomes. Methods: A retrospective cross-sectional study of IBD patients treated at the National Guard Hospital over a seven-year period was conducted. Data on demographics, body mass indices (BMIs), hospitalizations, comorbidities, complications, and surgical interventions were extracted from medical records. Associations between categorical and continuous variables were analyzed using chi-square and t-tests, respectively, with significance being set to p < 0.05. Results: A total of 465 patients were included: 54.6% had Crohn’s disease (CD) and 45.4% had ulcerative colitis (UC). CD predominated in males (60.6%), while UC was more common in females (55.5%, p = 0.001). BMI distribution differed significantly between groups (p = 0.004). Hospital admission rates and length of stay were higher among CD patients (p = 0.032). CD patients experienced greater complication rates, including fistulas (41.3% vs. 7.1%, p < 0.001) and strictures (26.1% vs. 1.4%, p < 0.001). Surgical interventions such as fistulotomy (4.3% vs. 0.5%, p = 0.009) and stricturoplasty (9.1% vs. 1.9%, p = 0.001) were more frequent in patients with CD. Conclusions: This study characterizes IBD patients in Saudi Arabia, highlighting gender differences, BMI variations, and the greater severity of CD compared with UC. The higher rates of complications and surgical interventions among CD patients emphasize the need for tailored management strategies. Future prospective studies are warranted to investigate disease progression and optimize care for this population.

Keywords: IBD, Crohn’s disease, ulcerative colitis, multimorbidity, hospitalization

1. Introduction

Multimorbidity is defined as co-occurrence of at least two chronic conditions in the same individual [1]. Multimorbidity is a significant global issue that is constantly growing and impacting patients, caregivers, society, and health systems and resource poor settings in particular [2,3]. Multimorbidity is distinct from the similar concept of comorbidity, which refers to the combined effects of additional conditions in relation to the primary condition in an individual [4,5]. In contrast, multimorbidity care is patient-centered and does not habitually prioritize any particular ailment, while in clinical care, patients and doctors will normally focus on the patient’s most pressing difficulties.

In contrast to people with a single chronic condition, people with multimorbidity have a higher probability of dying prematurely, experience constant hospital admissions and have an increased length of stay [6,7]. Multimorbidity is also associated with poorer function and health-related quality of life (HRQoL), depression, intake of multiple drugs (polypharmacy), and greater socioeconomic costs [8,9,10]

Inflammatory bowel disease (IBD) is signalized by repeated episodes of inflammation of the gastrointestinal tract caused by an abnormal immune response to gut microflora [11]. IBD encompasses two idiopathic conditions that affect the intestines; they are differentiated by their depth, involvement of the bowel wall, character, and location of inflammation [12].

Ulcerative colitis (UC) involves disseminated inflammation of the colonic mucosa. Almost always, UC affects the rectum in the form of proctitis, but it can manifest in the sigmoid (proctosigmoiditis), beyond the sigmoid (distal ulcerative colitis), or include the entire colon up to the cecum (pancolitis) [13]. Crohn’s disease (CD) results in transmural ulceration of any part of the gastrointestinal tract (GI), most often affecting the terminal ileum and colon. Both diseases are classified by extent (mild, moderate, or severe) and location. CD is also classified by inflammatory phenotype, structuring, and penetration [14].

In the mid-1990s, Hudson and 6 colleagues were among the first to consider IBD as an independent factor for increased cardiovascular risk [15]. Along with an increased prevalence of nonalcoholic fatty liver disease (NAFLD), obesity, chronic fatigue, and erectile dysfunction have been shown in patients with IBD [16,17,18]. Another paper showcased how common comorbidities among IBD patients are, as 78% of IBD patients had at least one comorbidity, with a median of three comorbidities [19]. As this showcases the global burden on healthcare systems around the world, especially in Saudi Arabia, or even the greater Middle East, we lack literature that targets and showcases multimorbidity in this region.

It warrants further effort and investigation into the subject; therefore, we aim to study the prevalence of multimorbidity in IBD patients and illustrate the association between multimorbidity and IBD patient characteristics and care outcomes in a tertiary care center in Riyadh, Kingdom of Saudi Arabia.

2. Materials and Methods

A retrospective cross-sectional study was conducted at National Guard Health Affairs (NGHA) Hospitals in Saudi Arabia. NGHA is a well-established healthcare institution offering a broad spectrum of clinical, academic, and research services, ranging from public health and primary care to specialized tertiary care. This study aimed to analyze the clinical characteristics and disease patterns among patients diagnosed with inflammatory bowel disease (IBD). Data were collected through a systematic chart review using a structured data collection sheet. The study population included Saudi adolescents and adults diagnosed with IBD between January 2016 and September 2022. Patients aged between 15 and 70 years were included in the study, while those aged 14 years and younger were excluded.

The study included all adult patients (≥18 years) with a confirmed diagnosis of Crohn’s disease or ulcerative colitis established through clinical evaluation, endoscopic findings, and radiologic or histopathologic confirmation. Only patients who visited gastroenterology, internal medicine, and general surgery clinics between January 2016 and December 2024 and had complete medical records were eligible. Individuals with active or follow-up visits were included, provided their clinical, laboratory, and imaging data were available for analysis. Patients were excluded if they had an indeterminate or unconfirmed diagnosis of inflammatory bowel disease. Patients younger than 18 years or those who received care primarily at another institution with insufficient documentation were not included in the analysis.

The study utilized a non-probability consecutive sampling technique, as all eligible patients meeting the inclusion and exclusion criteria were included due to the limited number of subjects. Data were extracted from the Best Care system, an electronic medical records platform used at NGHA, to ensure the accuracy and completeness of the variables. The variables collected included demographic characteristics such as age, gender, and body mass index (BMI), as well as clinical variables such as type of IBD based on the Montreal IBD classification, history of thromboembolism, disease relapse and severity, family history of IBD, smoking status, extraintestinal manifestations, hospital readmissions, age at disease onset, inflammatory complications, presence of primary sclerosing cholangitis, and biologic medication usage. The data were collected from Best Care system over the period between 19 April 2024 and 3 August 2024. Comorbidities were identified and extracted using International Classification of Diseases (ICD-10) diagnostic codes recorded at the time of each patient’s clinic visit or hospitalization. For each patient, all active ICD-10 codes listed in problem lists and encounter diagnoses were reviewed.

3. Results

A total of 465 patients were included in the study, with 54.6% being diagnosed with Crohn’s disease (CD) and 45.4% with ulcerative colitis (UC). The mean age of the total sample was 38.40 years old with a standard deviation (SD) of 14.60 years. The gender distribution showed a slightly higher proportion of males (53.3%) than females (46.7%). The majority of patients were Saudi nationals (97.2%), while only 2.8% were non-Saudis. Regarding medication usage, the distributions of non-biological and biological treatments were nearly equal, with 49.6% receiving non-biological therapy and 50.4% receiving biological therapy. Hospital admission duration varied among patients, with 47.7% never being admitted, 8.8% being admitted for 1–3 days, 19.7% for 4–7 days, 13.5% for 8–14 days, 7.1% for 15 days to one month, and 3.4% for more than one month (Table 1).

Table 1.

Baseline characteristics of the study population (N = 465).

Frequency
N (%)
Gender Female 217 (46.7)
Male 248 (53.3)
Age (Years) Mean (SD) 38.4 (14.6)
BMI Underweight 58 (12.5)
Normal weight 164 (35.3)
Overweight 125 (26.9)
Obese 118 (25.4)
Nationality Saudi 452 (97.2)
Non-Saudi 13 (2.8)
Medication Type Non-biological 230 (49.6)
Biological 234 (50.4)
Duration of Longest Admission Not admitted 222 (47.7)
1–3 days 41 (8.8)
4–7 days 90 (19.4)
8–14 days 63 (13.5)
15 days–1 month 33 (7.1)
>1 month 16 (3.4)
Diagnosis Crohn’s disease (CD) 254 (54.6)
Ulcerative colitis (UC) 211 (45.4)

Among the total cohort, 12.5% were classified as underweight, 35.3% as having a normal weight, 26.9% as overweight, and 25.4% as obese. This distribution highlights the significant variation in BMI among patients with inflammatory bowel disease (IBD) (Figure 1).

Figure 1.

Figure 1

Distribution of patients according to their BMI. Percentages may not sum to exactly 100% due to rounding to one decimal place.

The data collected were managed and analyzed using Statistical Package for Social Sciences (SPSS) version 25. Prior to analysis, data cleaning and coding were performed to ensure consistency and accuracy. Descriptive statistics were used to summarize categorical variables as frequencies and percentages, while continuous variables were expressed as means with standard deviations. To compare means and proportions, Student’s t-test and chi-square (χ2) tests were employed, respectively. Additionally, multivariate logistic regression analysis was conducted to identify factors associated with disease outcomes, including variables that demonstrated statistical significance at the bivariate level. A p-value of less than 0.05 was considered statistically significant for all analyses.

Higher comorbidity burden was significantly associated with older age (p < 0.001). Female patients were more likely to have ≥3 comorbidities compared with males (p = 0.002), and the prevalence of obesity increased progressively with comorbidity burden (p = 0.006). Use of non-biological therapy was more frequent among patients with a higher number of comorbidities (p = 0.003). Patients with ≥3 comorbidities experienced significantly longer hospital stays (p = 0.017), and readmission rates differed significantly across comorbidity groups (p = 0.019). Nationality was not associated with comorbidity burden. Crohn’s disease was more common among patients with a single comorbidity, whereas ulcerative colitis predominated in those with ≥3 comorbidities (p = 0.029) (Table 2).

Table 2.

Demographic and clinical characteristics of IBD patients stratified by comorbidity burden.

Comorbidities in IBD Patients Sig. Value
Patients with 1 Comorbidity
N (%)
Patients with 2 Comorbidities
N (%)
Patients with ≥3 Comorbidities
N (%)
Gender Female 51 (41.5) 32 (39.0) 77 (60.6) 0.002
Male 72 (58.5) 50 (61.0) 50 (39.4)
Age (Years) Mean (SD) 32.6 (10.7) 38.8 (13.3) 49.3 (16.4) <0.001
BMI Underweight 21 (17.1) 11 (13.4) 9 (7.1) 0.006
Normal weight 45 (36.6) 29 (35.4) 38 (29.9)
Overweight 32 (26.0) 26 (31.7) 30 (23.6)
Obese 25 (20.3) 16 (19.5) 50 (39.4)
Nationality Saudi 117 (95.1) 81 (98.8) 125 (98.4) 0.173
Non-Saudi 6 (4.9) 1 (1.2) 2 (1.6)
Medication Type Non-biological 51 (41.5) 43 (52.4) 80 (63.0) 0.003
Biological 72 (58.5) 39 (47.6) 47 (37.0)
Longest Admission Duration Not admitted 56 (45.5) 45 (54.9) 70 (55.1) 0.017
1–3 days 8 (6.5) 13 (15.9) 7 (5.5)
4–7 days 32 (26.0) 8 (9.8) 17 (13.4)
8–14 days 15 (12.2) 10 (12.2) 14 (11.0)
15 days–1 month 9 (7.3) 3 (3.7) 13 (10.2)
>1 month 3 (2.4) 3 (3.7) 6 (4.7)
Readmission No 80 (65.0) 67 (81.7) 97 (76.4) 0.019
Yes 43 (35.0) 15 (18.3) 30 (23.6)
Condition CD 72 (58.5) 40 (48.8) 53 (41.7) 0.029
UC 51 (41.5) 42 (51.2) 74 (58.3)

Anatomical involvement differed significantly by IBD type, with Crohn’s disease predominantly affecting the small intestine or presenting with combined intestinal involvement, whereas ulcerative colitis was largely confined to the large intestine (p < 0.001). Extra-intestinal anatomical involvement was more frequently observed in ulcerative colitis, particularly rectal involvement (p < 0.001). Metabolic comorbidities, including diabetes mellitus, hyperlipidemia, and hypertension, were significantly more prevalent among patients with ulcerative colitis compared with those with Crohn’s disease (p = 0.011, p < 0.001, and p = 0.004, respectively). Endocrine disorders, most notably hypothyroidism, were also more common in ulcerative colitis (p = 0.002). In addition, primary sclerosing cholangitis demonstrated a strong association with ulcerative colitis (p < 0.001). Smoking was significantly more prevalent among patients with Crohn’s disease (p = 0.007), whereas stroke occurred more frequently in patients with ulcerative colitis (p = 0.014) (Table 3).

Table 3.

Association of clinical characteristics and comorbidities with IBD types among patients.

Type of IBD Sig. Value
CD
N (%)
UC
N (%)
Total
N (%)
Anatomical involvement No data 7 (2.8) 15 (7.1) 23 (4.9) <0.001
Small intestine 55 (21.7) 12 (5.7) 67 (14.4)
Large intestine 22 (8.7) 139 (65.9) 161 (34.6)
Both 134 (52.8) 14 (6.6) 148 (31.8)
Unspecified 36 (14.2) 30 (14.2) 66 (14.2)
Extra-intestinal anatomical involvement None 212 (83.5) 142 (67.3) 354 (76.1) <0.001
Esophagus 4 (1.6) 2 (0.9) 6 (1.3)
Stomach 8 (3.1) 8 (3.8) 16 (3.4)
Rectum 22 (8.7) 57 (27.0) 79 (17.0)
Oral 8 (3.1) 2 (0.9) 10 (2.2)
Extra-GI manifestations None 228 (89.8) 184 (87.2) 412 (89.2) 0.110
Hepatobiliary 3 (1.2) 12 (5.7) 15 (3.3)
Ocular 2 (0.8) 2 (0.9) 4 (0.9)
Skin 4 (1.6) 1 (0.5) 5 (1.1)
MSK 11 (4.3) 7 (3.3) 18 (3.1)
Others 7 (2.75) 3 (1.4) 10 (2.2)
GI Infection None 227 (89.4) 181 (85.8) 408 (87.7) 0.483
H. pylori 6 (2.4) 3 (1.4) 9 (1.94)
C. difficile 15 (5.9) 16 (7.6) 31 (6.7)
Tuberculosis 3 (1.2) 2 (0.9) 5 (1.1)
CMV 2 (0.8) 6 (2.8) 8 (1.7)
Salmonella 1 (0.4) 1 (0.5) 2 (0.4)
C. perfringens 0 (0.0) 1 (0.5) 1 (0.2)
Brucellosis 0 (0.0) 1 (0.5) 1 (0.2)
Renal disease None 248 (97.6) 199 (94.3) 447 (96.1) 0.142
CKD 6 (2.4) 11 (5.2) 17 (3.7)
Nephrotic 0 (0.0) 1 (0.5) 1 (0.2)
Arthritis No 229 (90.2) 184 (87.2) 413 (88.8) 0.314
Yes 25 (9.8) 27 (12.8) 52 (11.2)
Diabetes No 225 (88.6) 169 (80.1) 394 (84.7) 0.011
Yes 29 (11.4) 42 (19.9) 71 (15.3)
Endocrine disorders None 246 (96.9) 186 (88.2) 432 (93.1) 0.002
Hypothyroidism 6 (2.4) 20 (9.5) 26 (5.6)
Hyperthyroidism 2 (0.8) 4 (1.9) 6 (1.3)
Hyperlipidemia No 240 (94.5) 169 (80.1) 409 (88.0) <0.001
Yes 14 (5.5) 42 (19.9) 56 (12.0)
Hypertension No 238 (93.7) 181 (85.8) 419 (90.1) 0.004
Yes 16 (6.3) 30 (14.2) 46 (9.9)
Anemia No 193 (76.0) 149 (70.6) 342 (73.55) 0.191
Yes 61 (24.0) 62 (29.4) 123 (26.45)
Vitamin D deficiency No 219 (86.2) 182 (86.3) 401 (86.24) 0.991
Yes 35 (13.8) 29 (13.7) 64 (13.76)
Vitamin B12 deficiency No 248 (97.6) 205 (97.2) 453 (97.42) 0.744
Yes 6 (2.4) 6 (2.8) 12 (2.58)
Primary sclerosing cholangitis No 251 (98.8) 187 (88.6) 438 (94.19) <0.001
Yes 3 (1.2) 24 (11.4) 27 (5.81)
Smoking No 222 (87.4) 199 (94.3) 425 (91.4) 0.007
Yes 26 (10.2) 8 (3.8) 40 (8.6)
Autoimmune diseases No 248 (97.6) 204 (96.7) 452 (97.20) 0.507
Psoriasis 4 (1.6) 4 (1.9) 8 (1.72)
Celiac disease 1 (0.4) 3 (1.4) 4 (0.86)
SLE 1 (0.4) 0 (0.0) 1 (0.22)
Stroke No 252 (99.2) 202 (95.7) 454 (97.63) 0.014
Yes 2 (0.8) 9 (4.3) 11 (2.37)
Psychiatric disorders No 237 (93.3) 196 (92.9) 433 (93.12) 0.860
Yes 17 (6.7) 15 (7.1) 32 (6.88)

The most common comorbidity among the patients was diabetes mellitus affecting 15.3% of the cohort. Other frequently reported conditions included anemia (13.80%), vitamin D deficiency (13.8%), and hyperlipidemia (12.0%). Hypertension was present in 9.9% of cases, followed by arthritis (11.2%) and psychiatric disorders (6.9%). Smoking was reported in 7.5% of patients. Autoimmune disorders such as psoriasis, celiac disease, and systemic lupus erythematosus (SLE) were uncommon, with respective prevalences of 2.8%, 1.7%, and 1.1% (Figure 2).

Figure 2.

Figure 2

Frequency of comorbidities.

CD patients had a significantly higher prevalence of perianal fistulas (18.1%) compared to UC patients (4.3%) (p < 0.001). Similarly, hemorrhoids were more common among CD patients (16.1%) than UC patients (9.0%) (p = 0.022). Anal abscesses were also significantly more frequent in CD patients (4.7%) compared to UC patients (1.4%) (p = 0.045). However, there were no significant differences between the two groups regarding anal fissures and anal strictures (Table 4).

Table 4.

Differences between CD and UC patients considering Hemorrhoid and perianal conditions.

Diagnosis
CD UC p-Value
Count Column
N %
Count Column
N %
Perianal Fistula No 208 81.9% 202 95.7% <0.001
Yes 46 18.1% 9 4.3%
Hemorrhoid No 213 83.9% 192 91.0% 0.022
Yes 41 16.1% 19 9.0%
Anal Fissure No 249 98.0% 208 98.6% 0.652
Yes 5 2.0% 3 1.4%
Anal Abscess No 242 95.3% 208 98.6% 0.045
Yes 12 4.7% 3 1.4%
Anal stricture No 252 99.2% 210 99.5% 0.674
Yes 2 0.8% 1 0.5%

CD patients exhibited a significantly higher incidence of complications compared to UC patients. Fistulas were more prevalent among CD patients (41.3%) compared to UC patients (7.1%) (p < 0.001). Similarly, strictures were significantly more common in CD patients (26.1%) than in UC patients (1.4%) (p < 0.001). Abscesses and bowel obstruction were also more frequent in CD patients, with abscesses occurring in 10.6% of CD cases compared to 1.4% in UC (p < 0.001) and bowel obstruction affecting 6.3% of CD patients versus 0.5% of UC patients (p = 0.001). Perforations were observed in 3.9% of CD cases compared to 0.9% of UC cases (p = 0.043). No significant differences were noted for adhesions and polyps between the two groups (Table 5).

Table 5.

Association of perianal conditions, complications, and surgical procedures with IBD subtype (Crohn’s disease vs. ulcerative colitis).

IBD Types Sig.
Values
CD
N (%)
UC
N (%)
Hemorrhoid and Perianal Conditions
Perianal Fistula No 208 (81.9) 202 (95.7) <0.001
Yes 46 (18.1) 9 (4.3)
Hemorrhoid No 213 (83.9) 192 (91.0) 0.022
Yes 41 (16.1) 19 (9.0)
Anal Fissure No 249 (98.0) 208 (98.6) 0.652
Yes 5 (2.0) 3 (1.4)
Anal Abscess No 242 (95.3) 208 (98.6) 0.045
Yes 12 (4.7) 3 (1.4)
Anal Stricture No 252 (99.2) 210 (99.5) 0.674
Yes 2 (0.8) 1 (0.5)
Different Complications
Fistula No 149 (58.7) 196 (92.9) <0.001
Yes 105 (41.3) 15 (7.1)
Strictures No 187 (73.9) 208 (98.6) <0.001
Yes 66 (26.1) 3 (1.4)
Adhesions No 251 (98.8) 211 (100.0) 0.113
Yes 3 (1.2) 0 (0.0)
Perforation No 244 (96.1) 209 (99.1) 0.043
Yes 10 (3.9) 2 (0.9)
Abscess No 227 (89.4) 208 (98.6) <0.001
Yes 27 (10.6) 3 (1.4)
Polyps No 247 (97.2) 202 (95.7) 0.374
Yes 7 (2.8) 9 (4.3)
Bowel obstruction No 238 (93.7) 210 (99.5) 0.001
Yes 16 (6.3) 1 (0.5)
Different Types of Surgeries
Fistulotomy No 243 (95.7) 210 (99.5) 0.009
Yes 11 (4.3) 1 (0.5)
Stricturoplasty No 231 (90.9) 207 (98.1) 0.001
Yes 23 (9.1) 4 (1.9)
Abscess drainage No 240 (94.5) 206 (97.6) 0.088
Yes 14 (5.5) 5 (2.4)
Ileocecal resection No 253 (99.6) 209 (99.1) 0.457
Yes 1 (0.4) 2 (0.9)
Hemicolectomy No 252 (99.2) 202 (95.7) 0.014
Yes 2 (0.8) 9 (4.3)
Proctocolectomy No 248 (97.6) 211 (100.0) 0.025
Yes 6 (2.4) 0 (0.0)
Total colectomy No 246 (96.9) 209 (99.1) 0.103
Yes 8 (3.1) 2 (0.9)
Subtotal colectomy No 245 (96.5) 206 (97.6) 0.461
Yes 9 (3.5) 5 (2.4)
Small bowel resection No 245 (96.5) 208 (98.6) 0.151
Yes 9 (3.5) 3 (1.4)
Ileocecectomy No 246 (97.2) 209 (99.1) 0.157
Yes 7 (2.8) 2 (0.9)

CD patients had significantly higher rates of fistulotomy (4.3% vs. 0.5%, p = 0.009) and stricturoplasty (9.1% vs. 1.9%, p = 0.001) compared to UC patients. Hemicolectomy was performed more frequently in UC patients (4.3%) than in CD patients (0.8%) (p = 0.014). Proctocolectomy was exclusively performed in CD patients (2.4%) but not in UC patients (p = 0.025). No significant differences were found in ileocecal resection, total colectomy, subtotal colectomy, small bowel resection, or abscess drainage between the two groups (Table 6).

Table 6.

Difference between CD and UC patients considering the type of surgery.

Diagnosis
CD UC p-Value
Count Column
N %
Count Column
N %
Fistulotomy No 243 95.7% 210 99.5% 0.009
Yes 11 4.3% 1 0.5%
Stricturoplasty No 231 90.9% 207 98.1% 0.001
Yes 23 9.1% 4 1.9%
Abscess drainage No 240 94.5% 206 97.6% 0.088
Yes 14 5.5% 5 2.4%
Ileocecal resection No 253 99.6% 209 99.1% 0.457
Yes 1 0.4% 2 0.9%
Hemicolectomy No 252 99.2% 202 95.7% 0.014
Yes 2 0.8% 9 4.3%
Proctocolectomy No 248 97.6% 211 100.0% 0.025
Yes 6 2.4% 0 0.0%
Total colectomy No 246 96.9% 209 99.1% 0.103
Yes 8 3.1% 2 0.9%
Subtotal colectomy No 245 96.5% 206 97.6% 0.461
Yes 9 3.5% 5 2.4%
Small bowl resection No 245 96.5% 208 98.6% 0.151
Yes 9 3.5% 3 1.4%
Ileocecectomy No 246 97.2% 209 99.1% 0.157
Yes 7 2.8% 2 0.9%

The associations between comorbidities (diabetes, hyperlipidemia, hypertension, and pancreatitis due to therapy) and the type and duration of hospital admission were analyzed. The duration of the longest hospital admission varied based on the presence of comorbidities. Notably, patients without diabetes had a higher percentage of not being admitted (55.1%), whereas those with type 1 diabetes had a slightly higher percentage (58.6%). However, all patients with type 2 diabetes required hospitalization for at least four days. The differences in admission duration among diabetes groups were not statistically significant (p = 0.316). Similarly, no significant associations were found between admission duration and hyperlipidemia (p = 0.146), hypertension (p = 0.352), or pancreatitis due to therapy (p = 0.066).

Regarding surgical interventions, hemicolectomy and subtotal colectomy showed significant associations with diabetes (p < 0.001), while ileocecectomy was significantly associated with pancreatitis due to therapy (p = 0.001). Other surgical procedures, such as fistulotomy, stricturoplasty, abscess drainage, ileocecal resection, and small bowel resection, did not show significant associations with any of the analyzed comorbidities (Table 7).

Table 7.

Associations of different comorbidities with admission duration and surgical procedures.

Duration of Longest Admission Diabetes Hyperlipidemia Hypertension Pancreatitis due to Therapy
Duration of Longest Admission Not admitted 217 (55.1) 218 (53.3) 226 (53.9) 257 (55.7)
1–3 days 30 (7.6) 30 (7.3) 33 (7.9) 34 (7.4)
4–7 days 68 (17.3) 71 (17.4) 71 (16.9) 75 (16.3)
8–14 days 47 (11.9) 50 (12.2) 50 (11.9) 53 (11.5)
15 days–1 month 20 (5.1) 27 (6.6) 26 (6.2) 28 (6.1)
>1 month 12 (3.0) 13 (3.2) 13 (3.1) 14 (3.0)
p-value 0.316 0.146 0.352 0.066
Fistulotomy Yes 25 (6.3) 24 (5.9) 25 (6.0) 26 (5.6)
p-value 0.975 0.618 0.426 0.744
Stricturoplasty Yes 18 (4.6) 18 (4.4) 19 (4.5) 19 (4.1)
p-value 0.501 0.878 0.656 0.099
Abscess drainage Yes 2 (0.5) 3 (0.7) 2 (0.5) 3 (0.7)
p-value 0.463 0.354 0.140 0.678
Ileocecal resection Yes 7 (1.8) 10 (2.4) 11 (2.6) 11 (2.4)
p-value 0.673 0.520 0.172 0.871
Hemicolectomy Yes 6 (1.5) 6 (1.5) 6 (1.4) 6 (1.3)
p-value <0.001 0.761 0.266 0.755
Proctocolectomy Yes 6 (1.5) 6 (1.5) 6 (1.4) 6 (1.3)
p-value 0.578 0.362 0.414 0.818
Total colectomy Yes 8 (2.0) 10 (2.4) 9 (2.1) 10 (2.2)
p-value 0.898 0.237 0.991 0.766
Subtotal colectomy Yes 10 (2.5) 14 (3.4) 13 (3.1) 14 (3.0)
p-value <0.001 0.160 0.726 0.723
Small bowel resection Yes 12 (3.0) 12 (2.9) 12 (2.9) 12 (2.6)
p-value 0.330 0.194 0.245 0.744
Ileocecectomy Yes 6 (1.5) 9 (2.2) 7 (1.7) 8 (1.7)
p-value 0.289 0.262 0.212 0.001

4. Discussion

The present study provided a comprehensive analysis of the clinical and demographic characteristics of inflammatory bowel disease (IBD) patients over the past three decades at a single referral center in Saudi Arabia. Our findings highlighted important differences in disease patterns, comorbidities, and treatment modalities between Crohn’s disease (CD) and ulcerative colitis (UC) patients, reflecting broader trends observed in global epidemiological studies.

The predominance of CD (54.6%) over UC (45.4%) in our cohort aligned with some regional studies suggesting an increasing prevalence of CD in Middle Eastern populations [19,20]. This distribution contrasted with Western populations, where UC had traditionally been more prevalent than CD [21]. The gender distribution revealed a male predominance (53.3%), with significant differences between CD and UC patients. CD was more common in males (60.6%), whereas UC was more prevalent in females (55.5%). This gender-based variation was consistent with prior research indicating a higher prevalence of CD in men and UC in women in some populations, possibly due to hormonal, genetic, and environmental factors [22,23].

As per our findings, patients with ≥3 comorbidities had longer hospital stays (p = 0.017). However, readmission rates differed significantly across comorbidity groups (p = 0.019). As reported by prior literature, predictive factors of readmission for ulcerative colitis were younger age, male sex, and transfusion [24]. For Crohn’s disease, chronic pain and younger age were predictive factors for readmission [25,26].

Obesity increased with comorbidity burden (p = 0.006). Moreover, according to prior literature, obesity is a factor associated with increased early readmission with higher burden, with prevention of obesity being a cornerstone to decrease readmission and health care burden [27]. In contrast, obesity was equally distributed among both CD and UC patients, which is consistent with emerging evidence suggesting a rising prevalence of obesity in IBD populations due to lifestyle changes and corticosteroid use [28].

Hospital admission patterns varied significantly between CD and UC patients. A higher proportion of UC patients had never been hospitalized (63.0%) compared to CD patients (49.2%), whereas CD patients experienced more prolonged hospital stays, with 4.7% requiring admission for over a month. This aligned with studies indicating that CD is associated with more severe disease progression, requiring frequent hospitalizations and surgical interventions [29,30].

Regarding anatomical involvement, a substantial proportion of CD patients exhibited both small and large intestine involvement (52.8%), reflecting the characteristic nature of CD as a transmural disease. UC is confined to patient’s large intestine. Extra-intestinal involvement was relatively uncommon, with rectal involvement being the most frequently reported (17.0%), followed by stomach (3.4%) and esophageal involvement (1.3%). These findings were consistent with previous literature, which emphasizes the heterogeneity of IBD manifestations and the potential for extra-intestinal complications [29].

Comorbid conditions were prevalent, with anemia (26.5%) being the most common, followed by endocrine disorders (22.6%) and vitamin D deficiency (13.8%). Anemia is a well-documented complication of IBD that is often attributed to chronic inflammation, gastrointestinal bleeding, and micronutrient deficiencies [31]. Endocrine disorders, particularly vitamin D deficiency, have been frequently reported in IBD patients and are thought to be linked to disease activity and immune dysregulation [32]. Adding on that, IBD and Type 2 Diabetes Mellitus have been linked throughout many studies. Furthermore, some studies described the association to be linked with steroid use while others determined that there was a correlation regardless of steroid use [33,34], which shows that more light needs to be shed on the matter.

A significant finding in our study was the higher prevalence of perianal fistulas (18.1% vs. 4.3%, p < 0.001), strictures (26.1% vs. 1.4%, p < 0.001), and absences (10.6% vs. 1.4%, p < 0.001) in CD patients compared to UC patients. This is in accordance with prior studies highlighting the aggressive nature of CD, which often necessitates surgical interventions due to complications such as fistulas, strictures, and abscess formation [35]. Additionally, CD patients underwent significantly higher rates of stricturoplasty (9.1% vs. 1.9%, p = 0.001) and fistulotomy (4.3% vs. 0.5%, p = 0.009), reinforcing the need for surgical management in refractory cases [36].

These findings emphasize the need for a multidisciplinary approach in managing IBD patients with comorbidities, as metabolic disorders can influence disease outcomes and surgical risks.

This study has several strengths, including a large sample size and a long-term retrospective analysis. However, limitations such as single-center design and retrospective nature may impact generalizability. Future multicenter studies are needed to validate our findings and explore additional factors influencing IBD progression in the Saudi population.

5. Conclusions

In conclusion, our findings provide valuable insights into the clinical, comorbidity, and disease burden characteristics of IBD patients in Saudi Arabia. The higher prevalence of CD, its association with more severe complications, and the significant role of comorbidities highlight the need for comprehensive disease management strategies. Further research should focus on identifying risk factors contributing to disease severity and optimizing therapeutic approaches to improve patient outcomes.

Limitations:

While consecutive sampling and EMR extraction provide a practical and real-world overview of IBD patient characteristics, the findings should be interpreted in light of potential selection bias, missing data, and documentation variability inherent to retrospective designs.

Abbreviations

The following abbreviations are used in this manuscript:

IBD Inflammatory Bowel Disease
CD Crohn’s Disease
UC Ulcerative Colitis
BMI Body Mass Index
NGHA National Guard Health Affairs
PSC Primary Sclerosing Cholangitis

Author Contributions

Conceptualization, W.A.; T.A.; N.K.A.; M.A.S.; N.S.A.; and A.B.A.; methodology, W.A.; T.A.; N.K.A.; M.A.S.; N.S.A.; and A.B.A.; software, M.A.S.; writing—original draft preparation, A.B.A. and S.A.; writing—review and editing, W.A.; N.A.R.; J.A.A.; and S.A.; supervision, N.A.R. and J.A.A.; project administration, N.A.R. and J.A.A.; investigation, W.A.; T.A.; N.K.A.; M.A.S.; and N.S.A.; visualization, A.B.A. and S.A. All authors have read and agreed to the published version of the manuscript.

Institutional Review Board Statement

The study was conducted in accordance with the Declaration of Helsinki and approved by the Ethics Committee of King Abdullah International Medical Research Center (IRB approval number: NRC23R/770/11) on 17 June 2025.

Informed Consent Statement

Patient consent was waived due to the retrospective nature and use of anonymized data.

Data Availability Statement

The original data presented in the study are openly available in FigShare at https://figshare.com/account/articles/30625409?file=59572733 (accessed on 7 November 2025).

Conflicts of Interest

The authors declare no conflicts of interest.

Funding Statement

This research received no external funding.

Footnotes

Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.

References

  • 1.Australian Institute of Health and Welfare . Chronic Condition Multimorbidity 2021: What is Multimorbidity and How Common Is It? Australian Institute of Health and Welfare; Canberra, Australia: 2021. [(accessed on 17 October 2023)]. Available online: https://www.aihw.gov.au/reports/chronic-disease/chronic-condition-multimorbidity-2021. [Google Scholar]
  • 2.Banerjee A., Hurst J., Fottrell E., Miranda J.J. Multimorbidity: Not Just for the West. Glob. Heart. 2020;15:35694. doi: 10.5334/gh.835. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 3.MacRae C., Morales D., Mercer S.W., Lone N., Lawson A., Jefferson E., McAllister D., Akker M.v.D., Marshall A., Seth S., et al. Impact of Data Source Choice on Multimorbidity measurement: A Comparison Study of 2.3 Million Individuals in the Welsh National Health Service. [(accessed on 17 October 2023)];BMC Med. 2023 21:309. doi: 10.1186/s12916-023-02970-z. Available online: https://pubmed.ncbi.nlm.nih.gov/37582755/#:~:text=Results%3A%20Using%20linked%20PC%2DHI. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 4.Nicholson K., Almirall J., Fortin M. The measurement of multimorbidity. Health Psychol. 2019;38:783–790. doi: 10.1037/hea0000739. [DOI] [PubMed] [Google Scholar]
  • 5.Harrison C., Fortin M., Akker M.v.D., Mair F., Calderon-Larranaga A., Boland F., Wallace E., Jani B., Smith S. Comorbidity versus multimorbidity: Why it matters. J. Multimorb. Comorbidity. 2021;11:3993. doi: 10.1177/2633556521993993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 6.Breen K., Finnegan L., Vuckovic K., Fink A., Rosamond W., DeVon H.A. Multimorbidity in Patients with Acute Coronary Syndrome Is Associated with Greater Mortality, Higher Readmission Rates, and Increased Length of Stay. J. Cardiovasc. Nurs. 2020;35:E99–E110. doi: 10.1097/JCN.0000000000000748. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 7.Rodrigues L.P., de Oliveira Rezende A.T., Delpino F.M., Mendonça C.R., Noll M., Nunes B.P., De Oliviera C., Silveira E.A. Association between multimorbidity and hospitalization in older adults: Systematic review and meta-analysis. Age Ageing. 2022;51:afac155. doi: 10.1093/ageing/afac155. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 8.Van Wilder L., Devleesschauwer B., Clays E., Pype P., Vandepitte S., De Smedt D. Polypharmacy and health-related quality of life/psychological distress among patients with chronic disease. [(accessed on 17 October 2023)];Prev. Chronic Dis. 2022 19:E50. doi: 10.5888/pcd19.220062. Available online: https://www.cdc.gov/pcd/issues/2022/22_0062.htm. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 9.Chang C.K., Chen Y.C., Chou Y.J., Chou P. Multimorbidity patterns and their association with depression: A population-based study. [(accessed on 18 October 2023)];Healthcare. 2025 13:1458. Available online: https://www.mdpi.com/2227-9032/13/12/1458. [Google Scholar]
  • 10.Tran P.B., Kazibwe J., Nikolaidis G.F., Linnosmaa I., Rijken M., van Olmen J. Costs of multimorbidity: A systematic review and meta-analyses. [(accessed on 18 October 2023)];BMC Med. 2022 20:234. doi: 10.1186/s12916-022-02427-9. Available online: https://bmcmedicine.biomedcentral.com/articles/10.1186/s12916-022-02427-9. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 11.McDowell C., Farooq U., Haseeb M. Inflammatory Bowel Disease. [(accessed on 18 October 2023)];2025 Available online: http://www.ncbi.nlm.nih.gov/pubmed/30137275. [PubMed]
  • 12.Maaser C., Sturm A., Vavricka S.R., Kucharzik T., Fiorino G., Annese V., Calabrese E., Baumgart D.C., Bettenworth D., Borralho Nunes P., et al. ECCO-ESGAR Guideline for Diagnostic Assessment in IBD Part 1: Initial diagnosis, monitoring of known IBD, detection of complications. J. Crohn’s Colitis. 2019;13:144–164. doi: 10.1093/ecco-jcc/jjy113. [DOI] [PubMed] [Google Scholar]
  • 13.Dmochowska N., Wardill H.R., Hughes P.A. Advances in Imaging Specific Mediators of Inflammatory Bowel Disease. Int. J. Mol. Sci. 2018;19:2471. doi: 10.3390/ijms19092471. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 14.Colombel J.-F., Shin A., Gibson P.R. AGA Clinical Practice Update on Functional Gastrointestinal Symptoms in Patients with Inflammatory Bowel Disease: Expert Review. Clin. Gastroenterol. Hepatol. 2019;17:380–390. doi: 10.1016/j.cgh.2018.08.001. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 15.Hudson M., Chitolie A., Hutton R.A., Smith M.S., Pounder R.E., Wakefield A.J. Thrombotic vascular risk factors in inflammatory bowel disease. Gut. 1996;38:733–737. doi: 10.1136/gut.38.5.733. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 16.Chalasani N., Younossi Z., LaVine J.E., Charlton M., Cusi K., Rinella M., Harrison S.A., Brunt E.M., Sanyal A.J. The diagnosis and management of nonalcoholic fatty liver disease: Practice guidance from the American Association for the Study of Liver Diseases. Hepatology. 2018;67:328–357. doi: 10.1002/hep.29367. [DOI] [PubMed] [Google Scholar]
  • 17.Friedman S., Magnussen B., O’Toole A., Fedder J., Larsen M.D., Nørgård B.M. Increased Use of Medications for Erectile Dysfunction in Men with Ulcerative Colitis and Crohn’s Disease Compared to Men Without Inflammatory Bowel disease: A Nationwide cohort Study. Am. J. Gastroenterol. 2018;113:1355. doi: 10.1038/s41395-018-0177-6. [DOI] [PubMed] [Google Scholar]
  • 18.D’Silva A., Fox D.E., Nasser Y., Vallance J.K., Quinn R.R., Ronksley P.E., Raman M. Prevalence and risk factors for fatigue in adults with inflammatory bowel disease: A systematic review with meta-analysis. Clin. Gastroenterol. Hepatol. 2022;20:995–1009. doi: 10.1016/j.cgh.2021.06.034. [DOI] [PubMed] [Google Scholar]
  • 19.Al-Fawzan A.A., Al-Radhi S.A., Al-Omar A.S., Al-Mutiri N.H., Al-Ammari A.M., El-Gohary M., Shamsan A.N., Al Shehri H.M., Alghasab N.S. A Study of the Epidemiology, Clinical, and Phenotypic Characteristics of Inflammatory Bowel Disease in the Northen-Central Region of Saudi Arabia. Diagnostics. 2023;13:2135. doi: 10.3390/diagnostics13132135. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 20.Burisch J. Crohn’s disease and ulcerative colitis. Occurrence, course and prognosis during the first year of disease in a European population-based inception cohort. [(accessed on 14 November 2025)];Dan. Med. J. 2014 61:B4778. Available online: http://www.ncbi.nlm.nih.gov/pubmed/24393595. [PubMed] [Google Scholar]
  • 21.Weisman M.H., Stens O., Kim H.S., Hou J.K., Miller F.W., Dillon C.F. Inflammatory Bowel Disease Prevalence: Surveillance data from the U.S. National Health and Nutrition Examination Survey. Prev. Med. Reports. 2023;33:102173. doi: 10.1016/j.pmedr.2023.102173. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 22.Rustgi S.D., Kayal M., Shah S.C. Sex-based differences in inflammatory bowel diseases: A review. Therap. Adv. Gastroenterol. 2020;13:15043. doi: 10.1177/1756284820915043. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 23.Massironi S., Viganò C., Palermo A., Pirola L., Mulinacci G., Allocca M., Peyrin-Biroulet L., Danese S. Inflammation and malnutrition in inflammatory bowel disease. Lancet Gastroenterol. Hepatol. 2023;8:579–590. doi: 10.1016/S2468-1253(23)00011-0. [DOI] [PubMed] [Google Scholar]
  • 24.Kunkle B., Singh H., Abraham D., Asamoah N., Barrow J., Mattar M. Independent predictors of 90-day readmission in patients with inflammatory bowel disease: A nationwide retrospective study. J. Crohns Colitis. 2025;19:jjaf034. doi: 10.1093/ecco-jcc/jjaf034. [DOI] [PubMed] [Google Scholar]
  • 25.Barnes E.L., Kochar B., Long M.D., Kappelman M.D., Martin C.F., Korzenik J.R., Crockett S.D. Modifiable risk factors for hospital readmission among patients with inflammatory bowel disease: A nationwide analysis. Inflamm. Bowel Dis. 2017;23:1332–1340. doi: 10.1097/MIB.0000000000001121. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 26.Ghahramani S., Tamartash Z., Sayari M., Vahedi H., Karimian F., Heydari S., Lankarani K.B. Risk factors affecting 90-day readmission of patients with inflammatory bowel disease. Middle East J. Dig. Dis. 2022;14:34–43. doi: 10.34172/mejdd.2022.253. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 27.Kaazan P., Seow W., Yong S., Heilbronn L.K., Segal J.P. The Impact of Obesity on Inflammatory Bowel Disease. Biomedicines. 2023;11:3256. doi: 10.3390/biomedicines11123256. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 28.Weissman S., Patel K., Kolli S., Lipcsey M., Qureshi N., Elias S., Walfish A., Swaminath A., Feuerstein J.D. Obesity in Inflammatory Bowel Disease Is Associated with Early Readmissions Characterised by an Increased Systems and Patient-level Burden. J. Crohn’s Colitis. 2021;16:1807–1815. doi: 10.1093/ecco-jcc/jjab088. [DOI] [PubMed] [Google Scholar]
  • 29.Tsai L., Nguyen N.H., Ma C., Prokop L.J., Sandborn W.J., Singh S. Systematic Review and Meta-Analysis: Risk of Hospitalization in Patients with Ulcerative Colitis and Crohn’s Disease in Population-Based Cohort Studies. Dig. Dis. Sci. 2022;67:2451–2461. doi: 10.1007/s10620-021-07200-1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 30.Niv Y. Hospitalisation of patients with Crohn’s disease: A systematic review and meta-analysis. Isr. Med. Assoc. J. 2020;22:111–115. doi: 10.1111/jgh.14953. [DOI] [PubMed] [Google Scholar]
  • 31.Mahadea D., Adamczewska E., Ratajczak A.E., Rychter A.M., Zawada A., Eder P., Dobrowolska A., Krela-Kaźmierczak I. Iron Deficiency Anemia in Inflammatory Bowel Diseases—A Narrative Review. Nutrients. 2021;13:4008. doi: 10.3390/nu13114008. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 32.Vernia F., Valvano M., Longo S., Cesaro N., Viscido A., Latella G. Vitamin D in Inflammatory Bowel Diseases. Mechanisms of Action and Therapeutic Implications. Nutrients. 2022;14:269. doi: 10.3390/nu14020269. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 33.Sang M.M., Sun Z.L., Wu T.Z. Inflammatory bowel disease and diabetes: Is there a link between them? World J. Diabetes. 2022;13:126–128. doi: 10.4239/wjd.v13.i2.126. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 34.Kang E.A., Han K., Chun J., Soh H., Park S., Im J.P., Kim J.S. Increased Risk of Diabetes in Inflammatory Bowel Disease Patients: A Nationwide Population-based Study in Korea. J. Clin. Med. 2019;8:343. doi: 10.3390/jcm8030343. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 35.Singh S., Picardo S., Seow C.H. Management of Inflammatory Bowel Diseases in Special Populations: Obese, Old, or Obstetric. Clin. Gastroenterol. Hepatol. 2020;18:1367–1380. doi: 10.1016/j.cgh.2019.11.009. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 36.Jiang K., Chen B., Lou D., Zhang M., Shi Y., Dai W., Shen J., Zhou B., Hu J. Systematic review and meta-analysis: Association between obesity/overweight and surgical complications in IBD. Int. J. Colorectal Dis. 2022;37:1485–1496. doi: 10.1007/s00384-022-04190-y. [DOI] [PMC free article] [PubMed] [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Data Availability Statement

The original data presented in the study are openly available in FigShare at https://figshare.com/account/articles/30625409?file=59572733 (accessed on 7 November 2025).


Articles from Clinics and Practice are provided here courtesy of Multidisciplinary Digital Publishing Institute (MDPI)

RESOURCES