Next Article in Journal
Infliximab and Plant-Based Diet as First-Line Therapy Followed by Corticosteroid Therapy for Severe Ulcerative Colitis: A Case Report
Previous Article in Journal
Retrospective Analysis of the Safety of FOLFOX Compared to CAPOX for Adjuvant Treatment of Stage III Colorectal Cancer in Newfoundland Patients
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Case Report

Onset of Ulcerative Colitis in a Patient with Type 2 Diabetes: Efficacy of a Plant-Based Diet for Both Diseases

1
Division of Gastroenterology, Akita City Hospital, Akita 010-0933, Japan
2
Division of Diabetes and Metabolism, Akita City Hospital, Akita 010-0933, Japan
3
Hatano Cardiology Clinic, Akita 010-0044, Japan
4
Takeda Clinic, Akita 010-0921, Japan
*
Author to whom correspondence should be addressed.
Gastrointest. Disord. 2022, 4(4), 223-229; https://doi.org/10.3390/gidisord4040021
Submission received: 17 August 2022 / Revised: 18 September 2022 / Accepted: 20 September 2022 / Published: 23 September 2022

Abstract

:
No case has been reported in which ulcerative colitis occurred in a patient with type 2 diabetes mellitus and the patient was treated with a plant-based diet. A 56-year-old man with a 3-year history of diabetes noticed bloody stool about 2 months after his worst glycated hemoglobin A1c test. Endoscopy revealed diffuse inflammation in the rectum. He was diagnosed with ulcerative colitis (proctitis, mild severity). He underwent educational hospitalization. A plant-based diet (1400 kcal/day) was provided. The same dosage of metformin was continued, but no medication was prescribed for ulcerative colitis. At the end of hospitalization, fecal occult blood 271 ng/mL became negative. Glycated hemoglobin A1c 6.9% had decreased to 6.6%. Two months after discharge, glycated hemoglobin A1c decreased to normal for the first time in 3.5 years. Ulcerative colitis had been in remission without medication for one and a half years after the educational hospitalization. Thereafter, however, he experienced two flareups. Deterioration in glycated hemoglobin A1c preceded the flareups. We described a scarcely reported case in which ulcerative colitis occurred in a patient with diabetes and the patient was treated with a plant-based diet. The plant-based diet was effective for both diseases. It seemed that the status of diabetes influenced the onset and relapse of ulcerative colitis.

1. Introduction

Inflammatory bowel disease (IBD) has been common in wealthy nations since the latter half of the 20th century, and it has increased since the turn of the 21st century in newly industrialized countries, thereby making IBD a global disease [1]. Type 2 diabetes (T2D) was a disease of the rich in the past [2]. However, it became one of the fastest growing health challenges of the 21st century, with the number of adults with T2D more than tripling over the past 20 years [3]. In Japan, increased incidence of IBD was associated with dietary transition (westernization) during high economic growth (1960–1975) [4]. The prevalence of IBD was 0.00089% of the population in 1975 [4], and it increased to 0.2% in 2015 [5]. The prevalence of T2D was 0.2% of the population in 1975 [3], and it increased to 6.7% in 2017 [6]. Therefore, both diseases have similar epidemiology, and their increases are associated with the contemporary lifestyle.
There are inconsistent results with respect to whether IBD is associated with increased risk for T2D. In a UK and Denmark cohort, individuals with ulcerative colitis (UC) showed an increased incidence of T2D compared to controls [7,8]. On the other hand, such an increase was not observed in South Korean and Taiwanese studies [9,10]. Conversely, there is scant information on whether T2D is associated with increased risk for IBD. At any rate, an association between IBD and T2D has been reported in the literature [7,8,9,10,11,12]. We encountered such a patient.
A plant-based diet (PBD) reduces the risk of T2D, and it is effective in the treatment of T2D [13,14,15]. PBDs have been shown to be more effective for glycemic control than conventional dietary guidelines recommended by nation-level diabetes organizations [16,17,18,19]. The American Diabetes Association recommends a plant-based diet (vegetarian diet) as one of the recommended diets for diabetes [14]. PBD is recommended also in Canada [20].
The etiology of IBD is generally stated as unknown. However, we regard a westernized diet in an affluent society as a ubiquitous environmental factor among various environmental factors underlying IBD [21]. We developed a PBD, i.e., a lacto-ovo-semi-vegetarian diet, to counter the westernized diet, and we have provided it to all inpatients with IBD starting in 2003 [22]. The modality incorporating PBD brought far better outcomes than the current modality in both UC and Crohn’s disease (CD), irrespective of disease stage (active or quiescent) [22,23,24,25,26]. Therefore, we recommend PBD for IBD [27].
To the best of our knowledge, no case has been reported in which UC occurred in a patient with T2D and the patient was treated with PBD.

2. Case Presentation

A 56-year-old self-employed man noticed bloody stool in late April 2020. At the same time, he felt mild stabbing pain in the left lower quadrant of the abdomen. Endoscopy revealed diffuse inflammation with numerous petechiae without a normal vascular pattern in the rectum (Figure 1A,B). Histologic examination revealed moderate infiltration of lymphocytes, plasma cells, and neutrophils. Non-caseating epithelioid granuloma was not found. Although crypt abscess was not found, neutrophils infiltration into glandular crypt epithelium was found. These findings were consistent with mild inflammation of UC. Stool culture did not reveal any pathogen. He was diagnosed with UC (initial onset, proctitis, mild severity) and referred to us. He accepted our advice and was admitted for educational hospitalization [28] mainly for ulcerative colitis, and secondarily for T2D and weight loss.
His height was 171.3 cm and body weight had been around 86 kg (body mass index (BMI) 29.3 kg/m2) for decades. He had a gout attack in 2002, and since then he took allopurinol. In 2010, he was diagnosed with obstructive apnea syndrome. Thereafter, he continued overnight treatment with continuous positive airway pressure. There was no family history of IBD in 2020, but his younger sister was diagnosed with UC in 2021, 1 year after his UC diagnosis.
His glycated hemoglobin A1c (HbA1c) (National Glycohemoglobin Standardization Program: reference 4.6–6.2%) was normal until 2013 (Figure 2). Then it fluctuated between 6.2% and 6.5% for a few years, but it increased to equal to or more than 6.6% in 2018; thereafter, metformin (500 mg/day) was prescribed for T2D (Figure 2). After starting medication, HbA1c decreased in three consecutive blood tests (Figure 2). However, it increased at each subsequent test up to a maximum of 7.3% in 2020 (Figure 2). Therefore, his physician (KH) warned him to drink less alcohol and eat less to reduce his body weight. He decreased his alcohol consumption from daily to twice a week. HbA1c decreased to 7.1% then to 6.9%. His body weight decreased to 84.2 kg (BMI 28.6 kg/m2). At 5 days prior to 6.9% HbA1c, he noticed bloody stool.
He was admitted for educational hospitalization for 9 days (Figure 2). On admission, he did not notice bloody stool. His weight was 82.1 kg (BMI 27.9 kg/m2). Physical examination was non-contributory, except for obesity. There was no abnormality in the following blood tests: total cholesterol, low- and high-density lipoprotein, serum albumin, uric acid, and C-reactive protein. Abnormalities were found in the following tests: HbA1c was 6.9% and triglyceride 343 mg/dL (reference 30–150). Fecal occult blood test was 271 ng/mL (<100).
PBD (1700 kcal/day), a lacto-ovo-semi-vegetarian diet with fish once a week and meat once every 2 weeks [22], was provided. Because inpatients were not allowed to go out for outdoor exercise due to COVID-19, the calorie count was decreased to 1400 kcal/day, and white rice was changed to brown rice on the 4th hospital day. Allopurinol, metformin, and overnight continuous positive airway pressure were continued. There was no medication for UC. On discharge, body weight, HbA1c, and triglyceride decreased to 81.3 kg (BMI 27.7 kg/m2), 6.6%, and 178 mg/dL, respectively (Figure 2). Fecal occult blood test became negative (68 ng/mL). He received dietary guidance on the PBD and was advised to continue the PBD after discharge [28].
In July 2020, 2 months after the discharge, HbA1c decreased to within the reference range for the first time since November 2015 (Figure 2). His body weight further decreased to 79.2 kg (BMI 26.9 kg/m2) (Figure 2). However, HbA1c increased above 6.2% for next half year without a rebound in body weight (Figure 2). His physician (KH) cautioned him against carelessness. He ate less and tried to increase his physical activity. Almost 1 year after the educational hospitalization, HbA1c reverted to within the normal range again without change in medication (Figure 2).
His plant-based diet score (PBDS), which evaluates adherence to PBD for Japanese patients with IBD [29] (a higher PBDS indicates greater adherence to the PBD), was 9 before admission and 35 during educational hospitalization. It was 24 at 13 months after discharge (Table 1).
About one and a half years after the discharge, he experienced bloody diarrhea 5–6 times/day (Figure 2). Sulfasalazine was administered, resulting in rapid remission. However, it was discontinued 7 days later due to gastric distress followed by typical adverse reactions to sulfasalazine, i.e., fever and generalized eruption. Three months later, he had another flareup (Figure 2). Ultrasonography did not show the wall thickness of the colon, indicating the absence of substantial extended inflammation beyond the rectum. Mesalazine rapidly induced remission in several days. He stated that he wanted to adhere to PBD, and he had taken meals as usual, but he might have been careless before the two flareups. HbA1c deteriorated before the flareups (Figure 2). There was no rebound in weight (Figure 2). No adverse or unanticipated events related to the PBD were observed over the course of treatment.

3. Discussion

We described a scarcely reported case in which UC occurred in a patient with T2D and the patient was treated with a plant-based diet. The PBD provided during educational hospitalization was effective for both diseases as expected. At the end of hospitalization, the amount of fecal occult blood decreased to a normal level. There was an improvement in HbA1c and BMI. Two months after discharge, HbA1c decreased to normal (5.8%) for the first time in 3.5 years.
The incidence of diet-related obesity and chronic diseases, including T2D, coronary heart disease, stroke, metabolic syndrome, and non-alcoholic fatty liver disease, has been steadily increasing and is a global health concern [30]. Classic socioeconomic transition toward an affluent society inevitably induces a dietary transition (westernization) [31,32]. However, the development of a food industry that produces foods rich in fats at low cost and urbanization have induced similar dietary westernization in lower-income countries [32]. Therefore, dietary westernization has occurred or is occurring all over the world. The transition has taken place in a shorter time in developing countries than in developed countries [32,33].
Current global consumption consists of an excess of unhealthy foods, such as red meat, sugar, and refined grains, and a shortage of healthy foods, such as vegetables, fruits, legumes, whole grains, and nuts [30]. This means that the current omnivorous (westernized) diet is problematic and should be corrected. Recent basic research clarifying an interrelationship between diet, gut microbiota, microbial metabolites, and health/disease has shown that current eating habits are pro-inflammatory, while PBD is anti-inflammatory [34,35,36,37]. Common features of consequences underlying the pathophysiology between IBD and T2D have been pointed out: gut dysbiosis, disrupted intestinal barrier function, close contact with pathogens followed by translocation of pathogens, increased pro-inflammatory cytokines and oxidative stress, endotoxemia, and low subclinical inflammation [38]. It is of note that symptoms of UC appeared 2 months after the highest HbA1c test result (Figure 2). In addition, two flareups occurred after deterioration of the HbA1c level (Figure 2). It seems that the status of T2D influences the onset and relapse of UC.
It is common that weight loss or decrease in HbA1c is greatest during or immediately after dietary intervention, but thereafter it increases toward the baseline in the long term (1 year). HbA1c was found to increase with either PBD or a diabetic diet [17,18]. It is remarkable that his HbA1c reverted to normal in our case, even in the long term (1 year) after educational hospitalization as a result of a lifestyle change by himself, not a change of medication (Figure 2). There was no rebound in body weight (Figure 2). He moderated all risk foods for Japanese patients with IBD (Table 1). The educational hospitalization seemed to enhance his awareness and perception of PBD, which resulted in the enhancement of his self-management skills.
A sister of the present patient was also affected by UC despite the rate of familial aggregation of IBD being low in Japan compared with other countries [39]. Therefore, it is anticipated that a genetic factor contributed more to the onset and clinical course in this patient than the average Japanese patients. However, a genetic study was not performed in this case.
In conclusion, we described a scarcely reported case in which UC occurred in a patient with T2D and the patient was treated with a plant-based diet. The PBD was effective for both diseases. Nowadays, it is apparent that current omnivorous diets cause the diet-related common chronic diseases, such as metabolic syndrome, T2D, coronary heart disease, stroke, and non-alcoholic fatty liver disease. We believe that IBD is not an exception. Basic medicine has supported the epidemiologic data of PBD over current westernized diets in health: current westernized diets are pro-inflammatory, while PBDs are anti-inflammatory. Greater appreciation of diet by care providers will change and improve the management of chronic diseases, including IBD and T2D.

Author Contributions

M.C. designed and conducted the study and wrote the manuscript. M.K., M.H., K.H. and M.T. contributed to the acquisition and interpretation of data and revision of the paper. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Institutional Review Board Statement

The study was conducted in accordance with the Declaration of Helsinki and approved by Akita City Hospital Ethical Committee (protocol number 15-2015, approved on 25 September 2015). Clinical trial registration: UMIN000019061 (Effect of a plant-based diet in inflammatory bowel disease) Registration: http://www.umin.ac.jp (accessed on 25 April 2022).

Informed Consent Statement

Written informed consent was obtained from the patient to publish this paper.

Data Availability Statement

The authors confirm that the data supporting the findings of this study are available within the article.

Conflicts of Interest

The authors declare no conflict of interest.

Abbreviations

BMIBody mass index
CDCrohn’s disease
HbA1cGlycated hemoglobin A1c
IBDInflammatory bowel disease
PBDPlant-based diet
PBDSPlant-based diet score
T2DType 2 diabetes
UCUlcerative colitis

References

  1. Kaplan, G.G.; Ng, S.C. Understanding and preventing the global increase of inflammatory bowel disease. Gastroenterology 2017, 152, 313–321. [Google Scholar] [CrossRef] [PubMed]
  2. Goto, Y. Epidemiological problems in diabetes mellitus. Tohoku J. Exp. Med. 1983, 141, 1–19. [Google Scholar] [CrossRef] [PubMed]
  3. International Diabetes Federation. IDF Diabetes Atlas, 9th ed.; 2019; Available online: https://diabetesatlas.org/en/ (accessed on 10 August 2021).
  4. Chiba, M.; Morita, N.; Nakamura, A.; Tsuji, K.; Harashima, E. Increased incidence of inflammatory bowel disease in association with dietary transition (Westernization) in Japan. JMA J. 2021, 4, 347–357. [Google Scholar] [PubMed]
  5. Murakami, Y.; Nishiwaki, Y.; Oba, M.S.; Asakura, K.; Ohfuji, S.; Fukushima, W.; Suzuki, Y.; Nakamura, Y. Estimated prevalence of ulcerative colitis and Crohn’s disease in Japan in 2015 An analysis of a nationwide survey. J. Gastroenterol. 2019, 54, 1070–1077. [Google Scholar] [CrossRef]
  6. Khan, M.A.B.; Hashim, M.J.; King, J.K.; Govender, R.D.; Mustafa, H.; Kaabi, J.A. Epidemiology of type 2 diabetes—Global burden of disease and forecasted trends. J. Epidemiol. Glob. Health 2020, 10, 107–111. [Google Scholar] [CrossRef] [PubMed]
  7. Dregan, A.; Charlton, J.; Chowienczyk, P.; Gulliford, M.C. Chronic inflammatory disorders and risk of type 2 diabetes mellitus, coronary heart disease, and stroke: A population-based cohort study. Circulation 2014, 130, 837–844. [Google Scholar] [CrossRef]
  8. Jess, T.; Jensen, B.W.; Andersson, M.; Villumsen, M.; Allin, K.H. Inflammatory bowel disease increases risk of type 2 diabetes in a nationwide cohort study. Clin. Gastroenterol. Hepatol. 2020, 18, 881–888. [Google Scholar] [CrossRef]
  9. 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. [Google Scholar] [CrossRef]
  10. Lai, S.-W.; Kuo, Y.-H.; Liao, K.-F. Association between inflammatory bowel disease and diabetes mellitus. Clin. Gastroenterol. Hepatol. 2020, 18, 1002–1003. [Google Scholar] [CrossRef]
  11. Tseng, C.-H. Metformin use is associated with a lower risk of inflammatory bowel disease in patients with type 2 diabetes mellitus. J. Crohn Colitis 2021, 15, 64–73. [Google Scholar] [CrossRef]
  12. Uwagbale, E.; Adeniran, O.G.; Adeniran, O.A.; Onukogu, I.; Agbroko, S.; Sonpal, N. In-hospital outcomes of inflammatory bowel diseases in patients with diabetes mellitus: A propensity score matching analysis. Cureus 2021, 13, e16566. [Google Scholar] [CrossRef] [PubMed]
  13. Trapp, C.; Barnard, N.; Katcher, H. A plant-based diet for type 2 diabetes: Scientific support and practical strategies. Diabetes Educ. 2010, 36, 33–48. [Google Scholar] [CrossRef] [PubMed]
  14. Evert, A.B.; Boucher, J.L.; Cypress, M.; Dunbar, S.A.; Franz, M.J.; Mayer-Davis, E.J.; Neumiller, J.J.; Nwankwo, R.; Verdi, C.L.; Urbanski, P.; et al. Nutrition therapy recommendations for the management of adults with diabetes. Diabetes Care 2014, 37 (Suppl. S1), S120–S143. [Google Scholar] [CrossRef] [PubMed]
  15. McMacken, M.; Shah, S. A plant-based diet for the prevention and treatment of type 2 diabetes. J. Geriatr. Cardiol. 2017, 14, 342–354. [Google Scholar]
  16. Barnard, N.D.; Cohen, J.; Jenkins, D.J.; Turner-McGrievy, G.; Gloede, L.; Jaster, B.; Seidl, K.; Green, A.A.; Talpers, S. A low-fat vegan diet improves glycemic control and cardiovascular risk factors in a randomized clinical trial in individuals with type 2 diabetes. Diabetes Care 2006, 29, 1777–1783. [Google Scholar] [CrossRef]
  17. Barnard, N.D.; Cohen, J.; Jenkins, D.J.; Turner-McGrievy, G.; Gloede, L.; Green, A.; Ferdowsian, H. A low-fat vegan and a conventional diabetes diet in the treatment of type 2 diabetes: A randomized, controlled, 74-wk clinical trial. Am. J. Clin. Nutr. 2009, 89, 1588S–1596S. [Google Scholar] [CrossRef]
  18. Kahleova, H.; Hill, M.; Pelikánova, T. Vegetarian vs. conventional diabetic diet—A 1-year follow-up. Cor et Vasa 2014, 56, e140–e144. [Google Scholar] [CrossRef]
  19. Lee, Y.-M.; Kim, S.-A.; Lee, I.-K.; Kim, J.-G.; Park, K.-G.; Jeong, J.-Y.; Jeon, J.-H.; Shin, J.-Y.; Lee, D.-H. Effect of a brown rice based vegan diet and conventional diabetic diet on glycemic control of patients with type 2 diabetes: A 12-week randomized clinical trial. PLoS ONE 2016, 11, e0155918. [Google Scholar] [CrossRef]
  20. Diabetes Canada Clinical Practice Guidelines Expert Committee; Sievenpiper, J.L.; Chan, C.B.; Dworatzek, P.D.; Freeze, C.; Williams, S.L. Nutrition therapy. Can. J. Diabetes 2018, 42 (Suppl. S1), S64–S79. [Google Scholar] [CrossRef]
  21. Chiba, M.; Nakane, K.; Komatsu, M. Westernized diet is the most ubiquitous environmental factor in inflammatory bowel disease. Perm. J. 2019, 23, 18–107. [Google Scholar] [CrossRef]
  22. Chiba, M.; Abe, T.; Tsuda, H.; Sugawara, T.; Tsuda, S.; Tozawa, H.; Fujiwara, K.; Imai, H. Lifestyle-related disease in Crohn’s disease: Relapse prevention by a semi-vegetarian diet. World J. Gastroenterol. 2010, 16, 2484–2495. [Google Scholar] [CrossRef] [PubMed]
  23. Chiba, M.; Tsuji, T.; Nakane, K.; Tsuda, S.; Ishii, H.; Ohno, H.; Watanabe, K.; Ito, M.; Komatsu, M.; Sugawara, T. Induction with infliximab and a plant-based diet as first-line (IPF) therapy for Crohn disease: A Single-group trial. Perm. J. 2017, 21, 17-009. [Google Scholar] [CrossRef] [PubMed]
  24. Chiba, M.; Nakane, K.; Tsuji, T.; Tsuda, S.; Ishii, H.; Ohno, H.; Watanabe, K.; Obara, Y.; Komatsu, M.; Sugawara, T. Relapse prevention by plant-based diet incorporated into induction therapy for ulcerative colitis: A single-group trial. Perm. J. 2019, 23, 18–220. [Google Scholar] [CrossRef] [PubMed]
  25. Chiba, M.; Tsuji, T.; Nakane, K.; Tsuda, S.; Ishii, H.; Ohno, H.; Obara, Y.; Komatsu, M.; Tozawa, H. High remission rate with infliximab and plant-based diet as first-line (IPF) therapy for severe ulcerative colitis: Single-group trial. Perm. J. 2020, 24, 166. [Google Scholar] [CrossRef] [PubMed]
  26. Chiba, M.; Tsuji, T.; Nakane, K.; Tsuda, S.; Ohno, H.; Sugawara, K.; Komatsu, M.; Tozawa, H. Relapse-free course in nearly half of Crohn’s disease patients with infliximab and plant-based diet as first-line (IPF) therapy: A Single-group trial. Perm. J. 2022, 26, 40–53. [Google Scholar] [CrossRef]
  27. Chiba, M.; Ishii, H.; Komatsu, M. Recommendation of plant-based diet for inflammatory bowel disease. Transl. Pediatr. 2019, 8, 23–27. [Google Scholar] [CrossRef]
  28. Chiba, M.; Nakane, K.; Tsuji, T.; Tsuda, S.; Ishii, H.; Ohno, H.; Watanabe, K.; Ito, M.; Komatsu, M.; Yamada, K.; et al. Relapse prevention in ulcerative colitis by plant-based diet through educational hospitalization: A single-group trial. Perm. J. 2018, 22, 17–167. [Google Scholar] [CrossRef]
  29. Chiba, M.; Nakane, K.; Takayama, Y.; Sugawara, K.; Ohno, H.; Ischii, H.; Tsuda, S.; Tsuji, T.; Komatsu, M.; Sugawara, T. Development and application of a plant-based diet scoring system for Japanese patients with inflammatory bowel disease. Perm. J. 2016, 20, 62–68. [Google Scholar] [CrossRef]
  30. Willett, W.; Rockström, J.; Loken, B.; Springmann, M.; Lang, T.; Vermeulen, S.; Garnett, T.; Tilman, D.; DeClerck, F.; Wood, A.; et al. Food in the Anthropocene: The EAT-Lancet Commission on healthy diets from sustainable food systems. Lancet 2019, 393, 447–492. [Google Scholar] [CrossRef]
  31. Fejfar, Z. Prevention against Ischaemic Heart Disease: A Critical Review. In Modern Trends in Cardiology—3; Oliver, M.F., Ed.; Butterworths: London, UK, 1974; pp. 465–499. [Google Scholar]
  32. Popkin, B.M. The nutrition transition in low-income countries: An emerging crisis. Nutr. Rev. 1994, 52, 285–298. [Google Scholar] [CrossRef]
  33. Zimmet, P. The global epidemiology of diabetes mellitus. Tohoku J. Exp. Med. 1983, 141, 41–54. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  34. De Filippo, C.; Cavalieri, D.; Di Paola, M.; Ramazzotti, M.; Poullet, J.B.; Massart, S.; Collini, S.; Pieraccini, G.; Lionetti, P. Impact of diet in shaping gut microbiota revealed by a comparative study in children from Europe and rural Africa. Proc. Natl. Acad. Sci. USA 2010, 107, 14691–14696. [Google Scholar] [CrossRef] [PubMed]
  35. Wu, G.D.; Chen, J.; Hoffmann, C.; Bittinger, K.; Chen, Y.-Y.; Keilbaugh, S.A.; Bewtra, M.; Knights, D.; Walters, W.A.; Knight, R.; et al. Linking long-term dietary patterns with gut microbial enterotypes. Science 2011, 334, 105–108. [Google Scholar] [CrossRef] [PubMed]
  36. David, L.A.; Maurice, C.F.; Carmody, R.N.; Gootenberg, D.B.; Button, J.E.; Wolfe, B.E.; Ling, A.V.; Devlin, A.S.; Varma, Y.; Fischbach, M.A.; et al. Diet rapidly and reproducibly alters the human gut microbiome. Nature 2014, 505, 559–563. [Google Scholar] [CrossRef]
  37. Sonnenburg, E.D.; Sonnenburg, J.L. Starving our microbial self: The deleterious consequences of a diet deficient in microbiota-accessible carbohydrates. Cell Metab. 2014, 20, 779–786. [Google Scholar] [CrossRef]
  38. Verdugo-Meza, A.; Ye, J.; Dadlani, H.; Ghosh, S.; Gibson, D.L. Connecting the dots between inflammatory bowel disease and metabolic syndrome: A focus on gut-derived metabolites. Nutrients 2020, 12, 1434. [Google Scholar] [CrossRef]
  39. Kitahora, T.; Utsunomiya, T.; Yokota, T. The Epidemiology Group of the Research Committee of Inflammatory Bowel Disease in Japan. Epidemiological study of ulcerative colitis in Japan: Incidence and familial occurrence. J. Gastroenterol. 1995, 30 (Suppl. S8), 5–8. [Google Scholar]
Figure 1. Endoscopic images of the rectum. (A) Diffuse inflammation without a normal vascular pattern was observed in the rectum. Numerous petechiae were seen. (B) A reverse view of the lower part of the rectum showing numerous yellow white spots and petechiae.
Figure 1. Endoscopic images of the rectum. (A) Diffuse inflammation without a normal vascular pattern was observed in the rectum. Numerous petechiae were seen. (B) A reverse view of the lower part of the rectum showing numerous yellow white spots and petechiae.
Gastrointestdisord 04 00021 g001
Figure 2. Chronological change of glycated hemoglobin A1c (%) and body mass index (kg/m2). The reference range for glycated hemoglobin A1c is 4.6–6.2% according to the National Glycohemoglobin Standardization Program. A body mass index higher than 25 is defined as obesity in Japan.
Figure 2. Chronological change of glycated hemoglobin A1c (%) and body mass index (kg/m2). The reference range for glycated hemoglobin A1c is 4.6–6.2% according to the National Glycohemoglobin Standardization Program. A body mass index higher than 25 is defined as obesity in Japan.
Gastrointestdisord 04 00021 g002
Table 1. Chronological change of plant-based diet score (PBDS).
Table 1. Chronological change of plant-based diet score (PBDS).
PBDS ScoringPBDS Measured Score in the Present Case
Food GroupsFrequency of ConsumptionBase
(Before Hospitalization)
Educational
Hospitalization
(9 Days)
13 Months
after
Discharge
Daily3–5 Times1–2 TimesRarely
/wk/wk0
Vegetables5310153
Fruits5310150
Pulses5310151
Potatoes/starches5310150
Rice5310555
Miso soup5310555
Green tea531000 *5
Yoghurt (plain)5310355
Meat−5−3−10−300
Minced or processed meat−5−3−10000
Cheese/butter/margarine−5−3−10−100
Sweets/ice cream/milk shake−5−3−10000
Soft drinks (cola/carbonated beverages/juice)−5−3−10000
Alcohol−5−3−10−100
Bread−5−3−10−100
Fish−2−100−200
Plant-based diet score (PBDS) 93524
* Green tea is recommended to drink at home but is not provided as a drink at the hospital.
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Share and Cite

MDPI and ACS Style

Chiba, M.; Komatsu, M.; Hosoba, M.; Hatano, K.; Takeda, M. Onset of Ulcerative Colitis in a Patient with Type 2 Diabetes: Efficacy of a Plant-Based Diet for Both Diseases. Gastrointest. Disord. 2022, 4, 223-229. https://doi.org/10.3390/gidisord4040021

AMA Style

Chiba M, Komatsu M, Hosoba M, Hatano K, Takeda M. Onset of Ulcerative Colitis in a Patient with Type 2 Diabetes: Efficacy of a Plant-Based Diet for Both Diseases. Gastrointestinal Disorders. 2022; 4(4):223-229. https://doi.org/10.3390/gidisord4040021

Chicago/Turabian Style

Chiba, Mitsuro, Masafumi Komatsu, Mihoko Hosoba, Kouji Hatano, and Masato Takeda. 2022. "Onset of Ulcerative Colitis in a Patient with Type 2 Diabetes: Efficacy of a Plant-Based Diet for Both Diseases" Gastrointestinal Disorders 4, no. 4: 223-229. https://doi.org/10.3390/gidisord4040021

Article Metrics

Back to TopTop