Skip to main content

ORIGINAL RESEARCH article

Front. Med., 19 April 2022
Sec. Gastroenterology
This article is part of the Research Topic Challenges in Inflammatory Bowel Disease: Current, Future and Unmet Needs View all 13 articles

Clinico-Epidemiological Characteristics of Patients With Inflammatory Bowel Disease in Egypt: A Nationwide Multicenter Study

\nMohamed ElbadryMohamed Elbadry1Mohamed O. Nour,Mohamed O. Nour2,3Mohamed HussienMohamed Hussien4Elsayed Awad GhoneemElsayed Awad Ghoneem5Mohammed A. MedhatMohammed A. Medhat6Hany ShehabHany Shehab7Sherif GalalSherif Galal8Mohamed EltabbakhMohamed Eltabbakh9Fathiya El-RaeyFathiya El-Raey10Mohamed NegmMohamed Negm7Shimaa AfifyShimaa Afify11Walaa AbdelhamedWalaa Abdelhamed12Ahmed SheriefAhmed Sherief9Ahmed AbdelazizAhmed Abdelaziz10Mohamed Abo ElkasemMohamed Abo Elkasem11Aya MahrousAya Mahrous4Ghada KamalGhada Kamal6Maha MaherMaha Maher5Omar Abdel-HameedOmar Abdel-Hameed5Abubakr ElbasunyAbubakr Elbasuny13Islam El-ZayyadiIslam El-Zayyadi5Ahmed BassionyAhmed Bassiony9Abdelmajeed MoussaAbdelmajeed Moussa14Essam BedewyEssam Bedewy15Asem ElfertAsem Elfert16Mohamed El Kassas
Mohamed El Kassas1*
  • 1Department of Endemic Medicine, Faculty of Medicine, Helwan University, Cairo, Egypt
  • 2Department of Public Health and Community Medicine, Damietta Faculty of Medicine, Al-Azhar University, Damietta, Egypt
  • 3Faculty of Public Health and Health Informatics, Umm Al-Qura University, Makkah, Saudi Arabia
  • 4Department of Gastroenterology, Hepatology and Infectious Diseases, Kafrelsheikh University, Kafrelsheikh, Egypt
  • 5Department of Hepatology and Gastroenterology, Mansoura University, Mansoura, Egypt
  • 6Department of Tropical Medicine and Gastroenterology, Assiut University, Assiut, Egypt
  • 7Integrated Clinical and Research Center for Intestinal Disorders (ICRID), Department and Endemic Medicine, Cairo University, Cairo, Egypt
  • 8Department of Tropical Medicine, Faculty of Medicine, Zagazig University, Zagazig, Egypt
  • 9Department of Tropical Medicine, Faculty of Medicine, Ain Shams University, Cairo, Egypt
  • 10Department of Hepatogastroenterology and Infectious Diseases, Damietta Faculty of Medicine, Al-Azhar University, Damietta, Egypt
  • 11Department of Gastroenterology, National Hepatology and Tropical Medicine Research Institute, Cairo, Egypt
  • 12Department Tropical Medicine and Gastroenterology, Sohag University, Sohag, Egypt
  • 13Department of Hepatology and Gastroenterology, Talkha Central Hospital, Talkha, Egypt
  • 14Department of Tropical Medicine and Gastroenterology, Faculty of Medicine, Aswan University, Aswan, Egypt
  • 15Department of Tropical Medicine, Faculty of Medicine, Alexandria University, Alexandria, Egypt
  • 16Department of Tropical Medicine and Infectious Diseases, Faculty of Medicine Tanta University, Tanta, Egypt

Background and Aims: Ulcerative colitis (UC) and Crohn's disease (CD) are the most common types of Inflammatory bowel disease (IBD), with variable responses to traditional therapies and unpredicted prognosis. In Egypt and most developing countries, the lack of recent epidemiological and prognostic data adversely affects management strategies. We collected and analyzed data of patients with IBD from multiple centers across Egypt to evaluate patients' clinical and epidemiological characteristics.

Methods: This retrospective multicenter study included patients diagnosed with IBD between May 2018 and August 2021, at 14 tertiary gastroenterology units across Egypt. Record analysis addressed a combination of clinico-epidemiological characteristics, biochemical tests, stool markers, endoscopic features, histological information, and different lines for IBD treatment.

Results: We identified 1104 patients with an established diagnosis of IBD; 81% of them had UC, and 19% showed CD. The mean age of onset was 35.1 ± 12.5 years ranging from 5 to 88 years, the mean duration of illness at inclusion was 13.6 ± 16.7 years, gender distribution was almost equal with a significant male dominance (60.4%, p = 0.003) among patients with CD, 57% were living in rural areas, and 70.5% were from Delta and Coastal areas. Two hundred nineteen patients (19.8%) displayed comorbid conditions, primarily associated with CD. The most frequent complaints were diarrhea (73.2%), rectal bleeding (54.6%) that was significantly higher among patients with UC (64%, p < 0.001), and 46.8% with abdominal pain (more often with CD: 71%, p < 0.001). Conventional therapy was effective in treating 94.7% of patients. The main lesion in patients with CD was ileal (47.8%); patients with UC mainly exhibited proctosigmoiditis (28.4%). Dysplasia was detected in 7.2% of patients, mainly subjects with UC.

Conclusions: To our knowledge, our effort is the first and largest cohort of Egyptian patients with IBD to describe clinical and epidemiological characteristics, and diagnostic and management approaches. More extensive prospective studies are still needed to fully characterize disease distribution, environmental factors, and pathological features of the disease.

Introduction

In 2017, 6.8 million Inflammatory bowel disease (IBD) cases were reported globally. The prevalence of IBD has increased substantially in many regions of the world, creating a substantial social and economic burden on health systems (1). Ulcerative colitis (UC) and Crohn's disease (CD) are major chronic IBD conditions in addition to indeterminate colitis that cause varying degrees of gastrointestinal (GI) tract inflammation. This classification was addressed by Montreal working party and commonly used in clinical practice and also for future serological and genetic studies in IBD (2). Data from several studies report a relationship between smoking and CD. However, quitting smoking may be accompanied by an increased risk of UC (3). Dietary fiber (particularly vegetables and fruits), saturated fats, sleep disorders, depression, and low vitamin D levels have been associated with increased IBD incidence. Also, stress, microbiota, some medications, such as NSAIDs, and early antibiotic exposure during infancy are factors that might increase the risk for IBD incidence, especially in genetically susceptible individuals (4, 5). Therefore, some studies concluded that, modification of one or more of these environmental factors has a bidirectional effect on the disease activity (6). Disease presentation includes signs and symptoms such as diarrhea, rectal bleeding, and abdominal pain. Fever, weight loss, extraintestinal symptoms, and fatigue may be observed (7). A serious complication of IBD is the malignant transformation of colonic mucosa that increases the incidence of colorectal carcinoma. Further, psychiatric health is negatively affected by IBD, especially in young patients (8). Also, extraintestinal manifestations (EIMs) can occur in some patients and affect joints, the hepatobiliary system, skin, and eyes (9).

Assessment of patients with IBD includes physical examination with a focus on extraintestinal complications, laboratory evaluation [C-reactive protein (CRP), erythrocytes sedimentation rate (ESR), and fecal calprotectin (FC)], endoscopy, and different imaging modalities (10). All these clinical examinations are used to confirm the diagnosis, gauge disease extent, and evaluate severity. Treatment depends on disease extent and severity (7).

The disease is a worldwide concern, but the incidence is highest in the United States, Sweden, and United Kingdom (1113). IBD has a growing incidence in the Middle East and North Africa; however, a lack of accurate registry and epidemiological cohort studies are still obstacles to evaluating the current situation (1416). UC is more common than CD in various parts of the world. In Egypt, few data regarding the epidemiology of IBD are available; however, some studies suggest the relative incidence ratio of UC and CD is 6:1 (17).

We conducted this retrospective cross-sectional multicenter study to represent all of Egypt. We collected clinical information to evaluate epidemiological characteristics, laboratory and imaging findings, colonoscopy results, and different treatment strategies. We aimed to assess updated data to draw a real map of IBD in Egypt in order to help us introduce scientific recommendations to optimize IBD diagnosis and management strategies.

Methods

Study Design, Settings, and Inclusion Criteria

This retrospective multicenter study was conducted on patients diagnosed with IBD at 14 tertiary GI units. These centers are affiliated with universities, distributed across Egypt, and represent the main geographical areas within the country where most of the Egyptian population is concentrated along the banks of the Nile River and on the river's delta including (1) Greater Cairo (Helwan, Cairo, Ain Shams, Al-Azhar, and the National Hepatology and Tropical Medicine Research Institute), (2) Delta region (Mansoura, Tanta, Zegazeg, and Kafr Elsheikh), (3) Coastal region (Alexandria and Damietta), (4) Upper Egypt (Sohag, Assiut, and Aswan). Patients from remote areas in Egypt, Sinai Peninsula, and Oases are largely referred to these tertiary centers. Data were collected both manually and electronically from available medical records between May 2018 and August 2021. Medical records of patients of all ages and both sexes with a confirmed diagnosis of IBD during the study period were enrolled.

Study Variables

Demographic features recorded were age of onset, gender, residence, geographic area, duration of illness, history of smoking, associated comorbidities, and other autoimmune diseases. Disease characteristics, including the severity of symptoms, presence of EIMs, type of medical treatment, and history of surgical intervention, were tabulated. Remission was defined as complete resolution of signs and symptoms, and endoscopic and histological healing of colon mucosa.

Diagnosis of IBD

The diagnosis of CD or UC was based on a combination of clinical manifestations, biochemical tests, stool markers, endoscopic features, and histological evaluation.

The recorded biochemical information included complete blood count (CBC), CRP, ESR, liver, and kidney function tests. Also, FC as a stool marker of intestinal inflammation was noted. Reports of abdominal ultrasonography and upper endoscopy were retrieved for all enrolled patients.

Endoscopic features consistent with UC were continuous and confluent colon inflammation with clear demarcation and rectal involvement. Endoscopic features consistent with CD were discontinuous lesions, mucosal nodularity, ulceration (both aphthous and linear), and strictures. Disease distribution and activity of UC were evaluated using the Montreal classification and Mayo score, respectively. While patients with CD were evaluated according to the severity of the onset of the disease using Harvey-Bradshaw score and Phenotypic distribution according to Montreal classification (2, 18).

Treatment of IBD

All recorded data about treatment approach either step up or step down, type of treatment either topical or systemic or biological in addition to antibiotic and steroid therapy were extracted from the patients‘ medical records and statistically analyzed.

Ethical Considerations

All procedures involving human participants were carried out according to the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki declaration and its later amendments, or comparable ethical standards. The study was approved by the Research Ethics Committee for human subject research at the Faculty of Medicine, Helwan University (Serial: 76-2021). The study data set was fully anonymized.

Statistical Analysis

Analysis used SPSS version 25.0 (IBM SPSS Statistics for Windows, Armonk, NY: IBM Corp., USA). Mean ± SD was used for quantitative variables, and frequency and percentage were used for qualitative variables. Mann-Whitney and Wilcoxon tests were used to assess the differences in means of quantitative non-parametric variables. Chi-square and Fisher's Exact tests were used to assess differences in the frequency of qualitative variables. The statistical methods assumed a significance level of p < 0.05 and a highly significant level of p < 0.001.

Results

The study included 1,104 patients with an established diagnosis of IBD. Ulcerative colitis was diagnosed in 81.3% of the study population, while −18.7% exhibited CD. The mean age of onset was 35.1 ± 12.5 years ranging from 5 to 88 years with mean duration of illness at inclusion of 13.6 ± 16.7 years for the cohort. The gender distribution was almost equal; however, a significant male dominance (60.4%, p = 0.003) was observed among patients with CD. The residence of the recruited patients was found to be in rural areas in 57% of cases. These patients displayed a higher prevalence of UC (59.2%, p = 0.002). Further, 70.5% were from North of Egypt. About of patients suffered from comorbid conditions, mainly hypertension (HTN) (9.1%) and diabetes (DM) (8.4%). Most comorbidities were more frequent among patients with CD, except for DM and other autoimmune diseases (Table 1).

TABLE 1
www.frontiersin.org

Table 1. General characteristics of patients with inflammatory bowel disease in Egypt (May 2018 to August 2021).

Clinical Presentations at Diagnosis

The most frequent manifestations, at the time of diagnosis, among all patients was diarrhea (73.2%) which was similar for both UC and CD. Bowel movements/day was 4.7 ± 2.2 ranging from 0 to 20. -Rectal bleeding was reported by 54.6% of patients, and it was significantly higher among UC subjects, while 48.6% -of patients complained from abdominal pain. Abdominal pain was higher among patients with CD, but the difference was insignificant. Weight loss was seen in 15.3% of patients, and 11.7% displayed EIM, mainly arthropathy. Fever was the least frequent symptom (8.5%) and was significantly higher among subjects with CD (Table 2).

TABLE 2
www.frontiersin.org

Table 2. Clinical characteristics of patients with inflammatory bowel disease in Egypt (May 2018 to August 2021).

Laboratory Investigations at Time of Diagnosis

Laboratory characteristics at the time of diagnosis showed significantly improved HB, CRP, ESR, WBC, and FC levels after treatment in both UC and CD patients (Table 3). PLT and AST were decreased in CD and UC patients, respectively. No notable change was observed in serum levels of total protein, albumin, and ALT.

TABLE 3
www.frontiersin.org

Table 3. Laboratory characteristics of patients with inflammatory bowel disease in Egypt (May 2018 to August 2021) before and after treatment.

Imaging, Endoscopic, and Histopathological Features of the Rectruited Patients

patients with patients with The lesions in CD subjects at diagnosis were mainly ileal (47.8%) and ileocolonic (38.6%). Lesions were mainly non-stricturing and non-penetrating (61.4%) and less commonly stricturing (20.8%) (Figure 1).

FIGURE 1
www.frontiersin.org

Figure 1. Distribution of the participating centers in the study across Egypt.

At diagnosis, CT/MRI revealed fistulization in about 11.1% of patients, and no abnormality was detected in about 18.4%. Colonoscopy showed proctosigmoiditis in 28.4% of patients with UC, proctitis in 25.1%, and pancolitis in 22.9%. Mild, moderate, and severe lesions were detected in 44.7, 35.8, and 19.5%, respectively (Figure 2).

FIGURE 2
www.frontiersin.org

Figure 2. Location and behavior of lesions by colonoscopy in patients with Crohn's disease in Egypt (May 2018 to August 2021) at the time of diagnosis.

Dysplasia was detected histologically in 80 patients (7.2%), mainly associated with UC (75 patients). Low-grade dysplasia was predominant, seen in 68 patients (6.2%). Sixty-four patients were diagnosed with UC (p = 0.012).

Lines of Management for the Recruited Patients

Most patients (94.7%) were managed using a step-up approach. The main antibiotics used were quinolone and metronidazole (40–50%). Topical therapies available in Egypt are (5-ASA suppositories and budesonide enema, and they) were used in 21–31% of cases. Unfortunately, other forms of topical therapies (5-ASA enemas, 5-ASA foams, 5-ASA gels, Corticosteroids foams, tacrolimus suppositories, and cyclosporin enemas) are not present in Egypt. Systemic treatment was prescribed for 50–86%, mainly with 5-ASA. About one-fourth received biological treatment, and only 2.6% were referred for coloniccolectomy or intestinal resection and anastomosis (Table 4).

TABLE 4
www.frontiersin.org

Table 4. Treatment characteristics of patients with inflammatory bowel disease in Egypt (May 2018 to August 2021).

Discussion

This study is the largest cohort evaluated for IBD in Egypt to the best of our knowledge. We found that the prevalent cases of UC are about four-fold greater than CD. This ratio is higher than reported elsewhere. In 2009, census data estimated that 1,171,000 Americans exhibited IBD (565,000 CD and 593,000 UC) (19). In 2018, the overall prevalence of IBD, CD, and UC in the UK were 725, 276, and 397 per 100 000 people, respectively (20). The occurrence of bleeding, which is more common in UC, is a potent stimulant for seeking medical advice, and so UC cases can be identified more frequently than CD cases. Furthermore, the diagnosis of CD may require exhaustive workup including detailed history taking, laboratory investigations, imaging modalities, and colonoscopy with ileal intubation or even enterostomy. These diagnostic facilities are expensive (not fully covered by insurance) and not available in all centers, particularly that more than half of our study population are from rural areas. However, such differences may be due to many factors that should be studied in community-based research. Key issues may be socioeconomic status, environmental conditions, and access to diagnostic and treatment facilities.

Our study's mean age of onset was 35 and 34 years for UC and CD subjects, respectively. The onset of IBD in adults was reported as 31–34 years in North America, Western Europe, and Oceania (2125). In Asia, the median age at diagnosis of CD was 34 years, and for UC was 42 years. UC was also found to start at more advanced ages, up to 79 years (26, 27).

The development of UC in our cohort was independent of gender, and however, CD was more common in males. These findings are consistent with epidemiological data from Europe, North America, and Oceania (2125). However, UC was more common in males in data from Asia (28).

More than half of the study population was from rural areas, inconsistent with the available literature on IBD demographics. The urban population in Egypt has been almost stable since 2010 and represents 42.8% of the Egyptian population (29). However, the lifestyle in rural areas has been urbanized, and this change should be studied selectively. Zuo et al. (30) indicated that rapid urbanization in the developing world is associated with an increasing incidence of several autoimmune diseases, including IBD. Urbanization impacts gut microbiota through westernization of diet, raised pollution levels, increased usage of antibiotics, and better hygiene status. A westernized diet is low in carbohydrates and high in animal proteins and fats. This diet will alter gut microbiota.

The clinical presentation of IBD in our cohort is consistent with globally published data. The predominant manifestations of UC were diarrhea, rectal bleeding, and mucous discharge from the rectum (31). Conversely, CD was characterized by prolonged intermittent diarrhea with abdominal pain (3235).

Ileal (47.8%) and ileocolonic (38.6%) regions were predominant sites of CD lesions, Colonic lesions were seen in (12.1%), while isolated upper GI CD was detected in only 1.4% of our study population. Slightly less than two-thirds of our patients (61.4%) showed non-complicated disease. Twenty-point eight percent exhibit stricturing CD, and 13.5% show penetrating CD. These data are consistent with data from Europe and North America, where 27–42% of patients with CD have ileal lesions at the time of diagnosis, 23–33% exhibit ileocolonic disease, 28–35% show colonic lesions, and only 1–6% of patients present with upper GI CD (24, 3639). Data from stricturing CD is estimated to occur in 29% and 19% of patients with CD in Europe (38) and North America (36), respectively. Conversely, Asian cohorts reported that more than half of patients with CD have an ileocolonic disease (4042).

Multiple serum biomarkers were evaluated for their ability to confirm the IBD disease type and to predict the disease course. The atypical antineutrophil cytoplasmic antibody (atypical pANCA) and anti-Saccharomyces cerevisiae antibody (ASCA) are the most studied antibodies in IBD patients. is most often expressed by patients with ulcerative colitis. Atypical pANCA is more common patients in patients with UC while ASCA in more frequent in CD patients (43). However, these tests are expensive and covered by health insurance, so they are commonly tested in Egypt.

Proctosigmoiditis was the most common disease site in UC cases in our cohort. Proctitis, left-sided colitis, and pancolitis were also seen in order of descending incidence. Most cases were mild to moderate at diagnosis. Disease extent and severity by colonoscopy in patients with ulcerative colitis are shown in Figure 3. Other cohorts showed that left-sided colitis was the most common disease site in Europe (39, 44).

FIGURE 3
www.frontiersin.org

Figure 3. Disease extent and severity by colonoscopy in patients with ulcerative colitis in Egypt (May 2018 to August 2021).

Most of our patients (96.3% of patients with UC and 87.4% of patients with CD) received conventional medical therapy as a first-line treatment even if they were indicated for biological therapy. The high costs of biological therapy likely limit its use, which may not be sustainable. However, health insurance and government-sponsored treatment have started to cover the costs of biological therapy at many centers in Egypt. Infliximab and adalimumab began to be used in 2013, and new biological therapies, such as ustekinumab have been used more recently (45).

Fortunately, conventional step-up therapy is a practical approach for treating Egyptian patients with IBD. Significant improvement in inflammatory markers, including CRP, ESR, and FC, were observed after treatment of both UC and CD.

Colorectal cancer is the most serious complication for patients with IBD, and dysplasia usually precedes the development of colorectal cancer (46). In our study, cases with confirmed dysplastic lesions constituted 7.2% of the total population. Most were low-grade and discovered on the first diagnosis.

Available evidence suggests that IBD incidence in Africa is increasing. Data are still lacking to understand the disease pattern across this continent. A few reports from North and South Africa are available (47).

The major strengths of our study are its large sample size and geographic diversity of patients, and collected data provide a comprehensive, updated picture of IBD in Egypt. Data describe differences in some clinical, epidemiological aspects of the disease. However, the study has some limitations. First, the distinction between UC and CD was not always clear. We depended on the most likely diagnosis from the treating physician. Lacking the distinction between IBD subtypes is a global problem. In a recently published population-based cohort study in European countries including 1,289 patients with IBD, the confirmation of IBD subtype was impossible in 7% of the study population, even after 5 years of follow-up (48). Second, the incomplete data for the follow-up of some patients did not allow us to track the changes in the disease patterns or to do a statistical analysis to see the histological features at time diagnosis will affect the outcome of our patients. Third, we may have missed early mild cases of IBD, especially in the private sector. Fourth, risk factors and environmental determinants of IBD were not discussed. Finally, certain socioeconomic factors, such as income and education, in addition to the yearly incidence of new cases could not be assessed.

Conclusion

To our knowledge, our study is the first Egyptian cohort study from multiple highly specialized GI centers from all over the country. It examines the largest cohort of Egyptian patients with IBD and describes the clinical, epidemiological presentation, diagnostic procedures, disease behavior, and prognostic implications along with available therapeutic options. The number of IBD cases was higher in rural than urban areas despite limited resources and relatively poor facilities in rural areas. More effort should be directed toward screening patients with IBD in rural areas for early detection and proper management of the disease. Such effort may relieve the burden of unexpected serious maladies. Step-up conventional therapy for patients with IBD is still recommended and effective, especially in countries with limited resources. More extensive prospective epidemiological studies in Egypt, other countries of the Middle East, and Africa are still needed to fully characterize disease distribution, environmental factors, and pathological features of IBD. Such data can be compared with other parts of the world to complete the global map of IBD and produce worldwide guidelines for managing this severe expanding disease.

Data Availability Statement

The raw data supporting the conclusions of this article will be made available by the authors, without undue reservation.

Ethics Statement

The studies involving human participants were reviewed and approved by Research Ethics Committee for human subject research at the Faculty of Medicine, Helwan University. Written informed consent for participation was not required for this study in accordance with the national legislation and the institutional requirements.

Author Contributions

MElb and MEK: study design. MON: data analysis. MElb, MON, MH, EG, MAM, HS, SG, MElt, FE-R,MN, SA,WA, AS, AA, MA, AMa, GK, MM, OA-H, AE, IE-Z, AB, AMo, EB, and AE: patient recruitment, data collection, and writing up of the first draft of the paper. All authors revised and approved the final version of the manuscript.

Conflict of Interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Publisher's Note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

References

1. GBD 2017 Inflammatory Bowel Disease Collaborators. The global, regional, and national burden of inflammatory bowel disease in 195 countries and territories, 1990-2017: a systematic analysis for the Global Burden of Disease Study 2017. Lancet Gastroenterol Hepatol. (2020) 5:17–30. doi: 10.1016/S2468-1253(19)30333-4

PubMed Abstract | CrossRef Full Text | Google Scholar

2. Satsangi J, Silverberg MS, Vermeire S, Colombel JF. The Montreal classification of inflammatory bowel disease: controversies, consensus, and implications. Gut. (2006) 55:749–53. doi: 10.1136/gut.2005.082909

PubMed Abstract | CrossRef Full Text | Google Scholar

3. Karban A, Eliakim R. Effect of smoking on inflammatory bowel disease: Is it disease or organ specific? World J Gastroenterol. (2007) 13:2150–2. doi: 10.3748/wjg.v13.i15.2150

PubMed Abstract | CrossRef Full Text | Google Scholar

4. Glassner KL, Abraham BP, Quigley EMM. The microbiome and inflammatory bowel disease. J Allergy Clin Immunol. (2020) 145:16–27. doi: 10.1016/j.jaci.2019.11.003

PubMed Abstract | CrossRef Full Text | Google Scholar

5. Ananthakrishnan AN. Epidemiology and risk factors for IBD. Nat Rev Gastroenterol Hepatol. (2015) 12:205–17. doi: 10.1038/nrgastro.2015.34

PubMed Abstract | CrossRef Full Text | Google Scholar

6. Vedamurthy A, Ananthakrishnan AN. Influence of environmental factors in the development and outcomes of inflammatory bowel disease. Gastroenterol Hepatol (N Y). (2019) 15:72–82.

PubMed Abstract | Google Scholar

7. Veauthier B, Hornecker JR. Crohn's disease: diagnosis and management. Am Fam Physician. (2018) 98:661–9.

Google Scholar

8. Bernstein CN, Benchimol EI, Bitton A, Murthy SK, Nguyen GC, Lee K, et al. The impact of inflammatory bowel disease in Canada 2018: extraintestinal diseases in IBD. J Can Assoc Gastroenterol. (2019) 2:S73–80. doi: 10.1093/jcag/gwy053

PubMed Abstract | CrossRef Full Text | Google Scholar

9. Seyedian SS, Nokhostin F, Malamir MD. A review of the diagnosis, prevention, and treatment methods of inflammatory bowel disease. J Med Life. (2019) 12:113–22.

PubMed Abstract | Google Scholar

10. Chen P, Zhou G, Lin J, Li L, Zeng Z, Chen M, et al. Serum biomarkers for inflammatory bowel disease. Front Med. (2020) 7:123. doi: 10.3389/fmed.2020.00123

PubMed Abstract | CrossRef Full Text | Google Scholar

11. Trallori G, Palli D, Saieva C, Bardazzi G, Bonanomi AG, d'Albasio G, et al. A population-based study of inflammatory bowel disease in Florence over 15 years (1978-92). Scand J Gastroenterol. (1996) 31:892–9. doi: 10.3109/00365529609051998

PubMed Abstract | CrossRef Full Text | Google Scholar

12. Logan RF. Inflammatory bowel disease incidence: up, down or unchanged? Gut. (1998) 42:309–11. doi: 10.1136/gut.42.3.309

PubMed Abstract | CrossRef Full Text | Google Scholar

13. Ehlin AG, Montgomery SM, Ekbom A, Pounder RE, Wakefield AJ. Prevalence of gastrointestinal diseases in two British national birth cohorts. Gut. (2003) 52:1117–21. doi: 10.1136/gut.52.8.1117

PubMed Abstract | CrossRef Full Text | Google Scholar

14. Mosli M, Alawadhi S, Hasan F, Abou Rached A, Sanai F, Danese S. Incidence, prevalence, and clinical epidemiology of inflammatory bowel disease in the Arab World: a systematic review and meta-analysis. Inflamm Intest Dis. (2021) 6:123–31. doi: 10.1159/000518003

PubMed Abstract | CrossRef Full Text | Google Scholar

15. Ponder A, Long MD. A clinical review of recent findings in the epidemiology of inflammatory bowel disease. Clin Epidemiol. (2013) 5:237–47. doi: 10.2147/CLEP.S33961

PubMed Abstract | CrossRef Full Text | Google Scholar

16. Molodecky NA, Soon IS, Rabi DM, Ghali WA, Ferris M, Chernoff G, et al. Increasing incidence and prevalence of the inflammatory bowel diseases with time, based on systematic review. Gastroenterology. (2012) 142:46–54.e42; quiz e30. doi: 10.1053/j.gastro.2011.10.001

PubMed Abstract | CrossRef Full Text | Google Scholar

17. Esmat S, El Nady M, Elfekki M, Elsherif Y, Naga M. Epidemiological and clinical characteristics of inflammatory bowel diseases in Cairo, Egypt. World J Gastroenterol. (2014) 20:814–21. doi: 10.3748/wjg.v20.i3.814

PubMed Abstract | CrossRef Full Text | Google Scholar

18. Lewis JD, Chuai S, Nessel L, Lichtenstein GR, Aberra FN, Ellenberg JH. Use of the noninvasive components of the Mayo score to assess clinical response in ulcerative colitis. Inflamm Bowel Dis. (2008) 14:1660–6. doi: 10.1002/ibd.20520

PubMed Abstract | CrossRef Full Text | Google Scholar

19. Kappelman MD, Moore KR, Allen JK, Cook SF. Recent trends in the prevalence of Crohn's disease and ulcerative colitis in a commercially insured US population. Dig Dis Sci. (2013) 58:519–25. doi: 10.1007/s10620-012-2371-5

PubMed Abstract | CrossRef Full Text | Google Scholar

20. Pasvol TJ, Horsfall L, Bloom S, Segal AW, Sabin C, Field N. etal. Incidence and prevalence of inflammatory bowel disease in UK primary care: a population-based cohort study. BMJ Open. (2020) 10:e036584. doi: 10.1136/bmjopen-2019-036584

PubMed Abstract | CrossRef Full Text | Google Scholar

21. Lakatos L, Kiss LS, David G, Pandur T, Erdelyi Z, Mester G, et al. Incidence, disease phenotype at diagnosis, and early disease course in inflammatory bowel diseases in Western Hungary, 2002-2006. Inflamm Bowel Dis. (2011) 17:2558–65. doi: 10.1002/ibd.21607

PubMed Abstract | CrossRef Full Text | Google Scholar

22. Vegh Z, Burisch J, Pedersen N, Kaimakliotis I, Duricova D, Bortlik M, et al. Incidence and initial disease course of inflammatory bowel diseases in 2011 in Europe and Australia: results of the 2011 ECCO-EpiCom inception cohort. J Crohns Colitis. (2014) 8:1506–15. doi: 10.1016/j.crohns.2014.06.004

PubMed Abstract | CrossRef Full Text | Google Scholar

23. Rönnblom A, Holmström T, Tanghöj H, Karlbom U, Thörn M, Sjöberg D. Low colectomy rate five years after diagnosis of ulcerative colitis. Results from a prospective population-based cohort in Sweden (ICURE) diagnosed during 2005-2009. Scand J Gastroenterol. (2016) 51:1339–44. doi: 10.1080/00365521.2016.1200141

PubMed Abstract | CrossRef Full Text | Google Scholar

24. Su HY, Gupta V, Day AS, Gearry RB. Rising incidence of inflammatory bowel disease in Canterbury, New Zealand. Inflamm Bowel Dis. (2016) 22:2238–44. doi: 10.1097/MIB.0000000000000829

PubMed Abstract | CrossRef Full Text | Google Scholar

25. Shivashankar R, Tremaine WJ, Harmsen WS, Loftus EV. Incidence and prevalence of Crohn's disease and ulcerative colitis in Olmsted county, minnesota from 1970 through 2010. Clin Gastroenterol Hepatol. (2017) 15:857–63. doi: 10.1016/j.cgh.2016.10.039

PubMed Abstract | CrossRef Full Text | Google Scholar

26. Yang SK, Yun S, Kim JH, Park JY, Kim HY, Kim YH et al. Epidemiology of inflammatory bowel disease in the Songpa-Kangdong district, Seoul, Korea, 1986-2005: a KASID study. Inflamm Bowel Dis. (2008) 14:542–9. doi: 10.1002/ibd.20310

PubMed Abstract | CrossRef Full Text | Google Scholar

27. Ng SC, Leung WK, Shi HY Li MK, Leung CM, Ng CK, et al. Epidemiology of inflammatory bowel disease from 1981 to 2014: results from a territory-wide population-based registry in Hong Kong. Inflamm Bowel Dis. (2016) 22:1954–60. doi: 10.1097/MIB.0000000000000846

PubMed Abstract | CrossRef Full Text | Google Scholar

28. Zeng Z, Zhu Z, Yang Y, Ruan W, Peng X, Su Y, et al. Incidence and clinical characteristics of inflammatory bowel disease in a developed region of Guangdong Province, China: a prospective population-based study. J Gastroenterol Hepatol. (2013) 28:1148–53. doi: 10.1111/jgh.12164

PubMed Abstract | CrossRef Full Text | Google Scholar

29. The World Bank. United Nations Population Division. World Urbanization Prospects: 2018 Revision. Urban population (% of total population)—Egypt, Arab Rep. (2018). Available online at: https://data.worldbank.org/indicator/SP.URB.TOTL.IN.ZS?locations=EG (accessed 09 October, 2021).

Google Scholar

30. Zuo T, Kamm MA, Colombel JF, Ng SC. Urbanization and the gut microbiota in health and inflammatory bowel disease. Nat Rev Gastroenterol Hepatol. (2018) 15:440–52. doi: 10.1038/s41575-018-0003-z

PubMed Abstract | CrossRef Full Text | Google Scholar

31. Kornbluth A Sachar DB Practice Practice Parameters Committee of the American College of Gastroenterology. Ulcerative colitis practice guidelines in adults: American College Of Gastroenterology, Practice Parameters Committee. Am J Gastroenterol. (2010) 105:501–23. doi: 10.1038/ajg.2009.727

PubMed Abstract | CrossRef Full Text | Google Scholar

32. Adams DH. Sleisenger and Fordtran's Gastrointestinal and Liver Disease. Gut. (2007) 56:1175. doi: 10.1136/gut.2007.121533

PubMed Abstract | CrossRef Full Text | Google Scholar

33. Thoreson R, Cullen JJ. Pathophysiology of inflammatory bowel disease: an overview. Surg Clin North Am. (2007) 87:575–85. doi: 10.1016/j.suc.2007.03.001

PubMed Abstract | CrossRef Full Text | Google Scholar

34. Panés J, Gomollón F, Taxonera C, Hinojosa J, Clofent J, Nos P. Crohn's disease: a review of current treatment with a focus on biologics. Drugs. (2007) 67:2511–37. doi: 10.2165/00003495-200767170-00005

PubMed Abstract | CrossRef Full Text | Google Scholar

35. Ko JK, Auyeung KK. Inflammatory bowel disease: etiology, pathogenesis and current therapy. Curr Pharm Des. (2014) 20:1082–96. doi: 10.2174/13816128113199990416

PubMed Abstract | CrossRef Full Text | Google Scholar

36. Peyrin-Biroulet L, Harmsen WS, Tremaine WJ, Zinsmeister AR, Sandborn WJ, Loftus EV. Surgery in a population-based cohort of Crohn's disease from Olmsted County, Minnesota (1970-2004). Am J Gastroenterol. (2012) 107:1693–701. doi: 10.1038/ajg.2012.298

PubMed Abstract | CrossRef Full Text | Google Scholar

37. Vester-Andersen MK, Prosberg MV, Jess T, Andersson M, Bengtsson BG, Blixt T, et al. Disease course and surgery rates in inflammatory bowel disease: a population-based, 7-year follow-up study in the era of immunomodulating therapy. Am J Gastroenterol. (2014) 109:705–14. doi: 10.1038/ajg.2014.45

PubMed Abstract | CrossRef Full Text | Google Scholar

38. Jeuring SF, van den Heuvel TR, Liu LY, Zeegers MP, Hameeteman WH, Romberg-Camps MJ, et al. Improvements in the long-term outcome of crohn's disease over the past two decades and the relation to changes in medical management: results from the population-based IBDSL cohort. Am J Gastroenterol. (2017) 112:325–36. doi: 10.1038/ajg.2016.524

PubMed Abstract | CrossRef Full Text | Google Scholar

39. Burisch J, Kiudelis G, Kupcinskas L, Kievit HAL, Andersen KW, Andersen V, et al. Natural disease course of Crohn's disease during the first 5 years after diagnosis in a European population-based inception cohort: an Epi-IBD study. Gut. (2019) 68:423–33. doi: 10.1136/gutjnl-2017-315568

PubMed Abstract | CrossRef Full Text | Google Scholar

40. Burisch J, Katsanos KH, Christodoulou DK, Barros L, Magro F, Pedersen N, et al. Natural disease course of ulcerative colitis during the first five years of follow-up in a European population-based inception cohort-an epi-IBD study. J Crohns Colitis. (2019) 13:198–208. doi: 10.1093/ecco-jcc/jjy154

PubMed Abstract | CrossRef Full Text | Google Scholar

41. Ng SC, Tang W, Ching JY, Wong M, Chow CM, Hui AJ, et al. Incidence and phenotype of inflammatory bowel disease based on results from the Asia-pacific Crohn's and colitis epidemiology study. Gastroenterology. (2013) 145:158–65.e2. doi: 10.1053/j.gastro.2013.04.007

PubMed Abstract | CrossRef Full Text | Google Scholar

42. Ng SC, Bernstein CN, Vatn MH, Lakatos PL, Loftus EV Jr, Tysk C, et al. Geographical variability and environmental risk factors in inflammatory bowel disease. Gut. (2013) 62:630–49. doi: 10.1136/gutjnl-2012-303661

PubMed Abstract | CrossRef Full Text | Google Scholar

43. Zhao J, Ng SC, Lei Y, Yi F, Li J, Yu L, et al. First prospective, population-based inflammatory bowel disease incidence study in mainland of China: the emergence of “western” disease. Inflamm Bowel Dis. (2013) 19:1839–45. doi: 10.1097/MIB.0b013e31828a6551

PubMed Abstract | CrossRef Full Text | Google Scholar

44. Roda G, Narula N, Pinotti R, Skamnelos A, Katsanos KH, Ungaro R, et al. Systematic review with meta-analysis: proximal disease extension in limited ulcerative colitis. Aliment Pharmacol Ther. (2017) 45:1481–92. doi: 10.1111/apt.14063

PubMed Abstract | CrossRef Full Text | Google Scholar

45. Eltabbakh M, Abd Alaty W, Sakr MA, Sherief AF. Commenting on the Letter (Completing the Picture in Egypt: Response to “Inflammatory Bowel Diseases in Egypt During the COVID-19 Pandemic”). Inflamm Bowel Dis. (2021) 27:e66. doi: 10.1093/ibd/izab009

PubMed Abstract | CrossRef Full Text | Google Scholar

46. Driessen A, Macken E, Moreels T, Jouret-Mourin A. Dysplasia in inflammatory bowel disease. Acta Gastroenterol Belg. (2017) 80:299–308.

Google Scholar

47. Hodges P, Kelly P. Inflammatory bowel disease in Africa: what is the current state of knowledge? Int Health. (2020) 12:222–30. doi: 10.1093/inthealth/ihaa005

PubMed Abstract | CrossRef Full Text | Google Scholar

48. Burisch J, Zammit SC, Ellul P, Turcan S, Duricova D, Bortlik M, et al. Disease course of inflammatory bowel disease unclassified in a European population-based inception cohort: An Epi-IBD study. J Gastroenterol Hepatol. (2019) 34:996–1003. doi: 10.1111/jgh.14563

PubMed Abstract | CrossRef Full Text | Google Scholar

Keywords: ulcerative colitis, Crohn's disease, multicenter study, Egypt, inflammatory bowel disease

Citation: Elbadry M, Nour MO, Hussien M, Ghoneem EA, Medhat MA, Shehab H, Galal S, Eltabbakh M, El-Raey F, Negm M, Afify S, Abdelhamed W, Sherief A, Abdelaziz A, Abo Elkasem M, Mahrous A, Kamal G, Maher M, Abdel-Hameed O, Elbasuny A, El-Zayyadi I, Bassiony A, Moussa A, Bedewy E, Elfert A and El Kassas M (2022) Clinico-Epidemiological Characteristics of Patients With Inflammatory Bowel Disease in Egypt: A Nationwide Multicenter Study. Front. Med. 9:867293. doi: 10.3389/fmed.2022.867293

Received: 31 January 2022; Accepted: 21 March 2022;
Published: 19 April 2022.

Edited by:

Antonietta G. Gravina, University of Campania Luigi Vanvitelli, Italy

Reviewed by:

Ivana Trivic, Children's Hospital Zagreb, Croatia
Boldeanu Mihail Virgil, University of Medicine and Pharmacy of Craiova, Romania

Copyright © 2022 Elbadry, Nour, Hussien, Ghoneem, Medhat, Shehab, Galal, Eltabbakh, El-Raey, Negm, Afify, Abdelhamed, Sherief, Abdelaziz, Abo Elkasem, Mahrous, Kamal, Maher, Abdel-Hameed, Elbasuny, El-Zayyadi, Bassiony, Moussa, Bedewy, Elfert and El Kassas. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Mohamed El Kassas, bV9lbGthc3NhcyYjeDAwMDQwO2hxLmhlbHdhbi5lZHUuZWc=

Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.