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"The term "Inflammatory Bowel Disease" (IBD) is frequently used to denote two diseases, ulcerative colitis (UC) and Crohn's disease (CD). This condition is frequently recorded in the West, and along with development of diagnostic facilities, is beginning to be more commonly found in Indonesia.The etiology of this disease is still unclear, but it is suspected that environmental, geographic, and genetic factors are involved. Cytokines play a great role in the pathogenesis of IBD, where in IBD there is an unbalance of pro-inflammatory cytokines and inhibitor cytokines. In IBD, there is an increase in pro-inflammatory cytokines, such as IL-1, IL-2, IL-6, IL-8, and alpha TNF in the intestinal mucosa. Such increase significantly correlates with the activity of ulcerative colitis through endoscopic examination,At this moment, forms of therapy for IBD associated with cytokines are being developed, such as ways to inhibit cytokine synthesis, cytokine release, cytokine activity and the cytokine signaling pathway in the target cell."

"The pathogenesis of inflammatory bowel disease (IBD) is not yet fully understood A genetic predisposition, some environmental factors and microbial flora of the grit are the key factors. The presence of bacteria in the intestinal lumen is a prerequisite for the development of IBD. In animal models, mice incapable of expressing IL, or IL invariably develop a colitis- or Crohn-like inflammation. No inflammation occurs if they grow up in a pathogen free environment or if they are fed with Lactobacillus sp when exposed to environmental bacteria. Thus, the absence of liminal bacteria or a different make-up there of prevents the development of inflammatory bowel disease in this model. Patients with IBD have been found to have a decreased stool excretion Lactobacillus andlor Bifidobacteria. Furthermore, an increased number of bacteria adherents to the mucosa and within the epithelium has been demonstrated in quantitative studies. It appears that these bacteria trigger a strong abnormal mucosal immunological response, leading to intestinal epithelial cell injury mediated by activated T-cells, mononuclear cells and macrophages. If this response can not be down regulated by regulatory T-cells, mononuclear inflammatory cytokines are activated by stimulation of the intracellular transcription factor NF-kB. Recently it was shown that bacterial lipopolysaccharides can activate NF-kB by binding to two specific receptors on the cell membrane (Toll-like receptors [TLR's]) or intracellular receptors (NOD's). New insights of the role of bacteria in IBD became available by identifying susceptibility genes for IBD. Several IBD susceptibility loci were recently identified. The IBD-l locus on chromosome 16 shows positive evidence for linkage in Crohn's disease and IBD-2 locus on chromosome l2 for ulcerative colitis. The evidence for' an association with Crohn's disease at the IBD-I locus have been shown to be attributed to mutations in the CARDI5/NOD2 gene. This gene is exressed in peripheral blood monocytes and in intestinal epithelial cells and serves as a key factor of innate mucosal response to luminal bacteria as an antibacterial factor. The intact intercellular NOD2 protein binds LPS and activates NF-kB. This activation of the NF-kB signalling pathway in response to bacterial components plays a protective role in the mucosal epithelial cells for the host against inviting pathogens and an increased apoptosis of infected cells. There is evidence, that the defective NOD2 protein variants increase the susceptibility to pathogen invasion and a decrease in cellular apoptosis. NF-kB plays a dual role in IBD. On the mucosal epithelial cells, bacterial components bind on NOD2 proteins and protect bacterial invasion. If this barrier mechanism is not intact, the bacterial invasion stimulates via TLR- and NOD2 receptors in immune-active cells (macrophages, T-cells and monocytes) NF-kB and triggers an aberrant inflammatory response leading to tissue damage. These new insights in the pathogenesis in IBD have led to new treatment possibilities including pre- and probiotics. These therapies are aimed at directly modulating the host immune system to suppress intestinal inflammation. This has prompted considerable interest in manipulating the enteric microenvironment as a novel therapeutic strategy Several clinical studies showed promising results rising pre- and probiotics in patients with ulcerative colitis, pouchitis and Crohn's disease. The introduction of genetically engineered probiotic organism to produce and deliver anti-inflammatory cytokines or other biological relevant molecules to the mucosa offers further new potential for the treatment of IBD."

"Inflammatory bowel disease (IBD) has begun to emerge in Indonesia. The disease is further classified into two types, ulcerative colitic (UC) and crohn's disease (CD). Diagnosis of IBD is initiated from symptom findings such as diarrhea, abdominal pain, bleeding diarrhea, and weight loss, and supported by physical examination and additional tests. The options for additional examinations of IBD are mainly endoscopy (esophagogastroduodenoscopy, colonoscopy, and also intestinal endoscopy), imaging the techniques and laboratory examinations either from blood or feces. The application of these modalities should be prompted by sufficient clinical suspicion to promote their efficiency as well as prevent underdiagnosis or overdiagnosis. In primary health care settings, patients with IBD are expected to be recognized for therapy or to use appropriate referral system to warrant a proper treatment."

"Inflammatory bowel disease (IBD) in rarely found in clinical practice. However, the incidence of IBD seems to have increased recently. Generally, the patients will come to hospital with chief complain! of chronic diarrhea with or without hematochezia.We reported two cases of IBD in which they had been misdiagnosed as colitis tuberculosis based on colonoscopy examination. Treatment of anti tuberculosis drugs had made no clinical improvement. Further evaluation suggested the diagnosis of IBD. They responded very well clinically after treated as IBD. This case report reminds us to consider the diagnosis of IBD in patient with chronic diarrhea and ulceration in colonic mucosa at colonoscopy."

"Latar Belakang/Tujuan: Pasien IBD berisiko terjadi defisiensi Zink. Sedangkan Zink memiliki peran dalam menstimulasi sistem imun, regenerasi sel, dan berperan sebagai koenzim yang berperan sebagai antioksidan. Pemberian suplementasi Zink diharapkan dapat menurunkan aktivitas penyakit dan meningkatkan aktivitsas antioksidan.Metode: Penelitian ini merupakan kajian sistematis dan meta-analisis. Pencarian literatur dilakukan sampai desember 2020 dengan mencari pada tiga database yaitu Cochrane central, Pubmed, dan Embase. Berdasarkan kriterian eligibilats didapatkan 9 artikel yang menilai efek Zink terhadap aktivitas penyakit IBD. Aktivitas penyakit dinilai berdasarkan skor CDAI dan skor Mayo, serta aktivitas enzim SOD.Hasil: Sebanyak 9 studi didapat dari pencarian, dilakukan analisis kualitatif dan kuantitatif. Meta-analisis dilakukan dengan membagi menjadi 3 subgrup, yaitu Zink terhadap aktivitas penyakit IBD, Zink terhadap aktivitas enzim SOD, serta aktivitas penyakit sebelum dan sesudah pemberian. Empat studi menilai efek Zink terhadap aktivitas penyakit menunjukkan tidak terdapat penutunan aktivitas penyakit IBD, dua studi menilai efek Zink terhadap aktivitas SOD menunjukkan tidak terdapat peningkatan aktivitas SOD, dua studi menilai efek Zink terhadap ekspresi metalotinonin datu studi menunjukkan peningkatan dan satu studi tidak menunjukkan peningkatan. Tiga studi pre dan post dari dua studi menunjukkan tidak terdapat penurunan aktivitas penyakit dan 1 studi menunjukkan penurunan aktivitas jika diberikan jangka panjang.Simpulan: Tidak didapatkan perbedaan aktivitas penyakit, aktivitas SOD, aktivitas metalotionin dengan suplementasi Zink jangka pendek, suplementasi jangka panjang dapat menurunkan aktivitas penyakit IBD

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Background/Aim: IBD patients are at risk of Zinc deficiency. Zinc has a role in stimulating the immune system, cell regeneration, and as a coenzyme acts as an antioxidant. Zinc supplementation will decrease disease activity and increase antioxidant activity.

Method: This research is a systematic review and meta-analysis. Literature searches are conducted until December 2020, we searched in three databases Cochrane central, Pubmed, and Embase. Based on eligibility criteria, there are 9 articles evaluate effect of Zinc on disease activity of IBD. Disease activity is assessed based on CDAI score and Mayo score, as well as SOD enzyme activity.

Result: We identified 9 studies, Of all the potentially relevant papers, 9 studies were identified. All of the studies were assessed for risk of bias along with qualitative analysis. Pre-specified outcomes were Zinc and disease activity, Zinc and SOD activity, metallothionine expression as well as disease activity before and after administration. Four studies evaluated effect of Zinc on disease activity showed no improvement in IBD disease activity, two studies evaluated effect of Zinc on SOD activity showed no increase in SOD activity, two studies evaluated effect of Zinc on metalotinonin expression, one study showed increase of expression and the other had no increase. There are 3 pre and post studies from two studies showed no decrease in disease activity and 1 study showed a decrease in activity if supplemented for long term.

Conclusion: The results of the systematic review revealed there were no difference in disease activity, SOD and methalotionen activity with short term Zinc supplementation, long term supplementation decrease disease activity of IBD"

"Latar Belakang. Vitamin D merupakan salah satu komponen regulator yang berperan dalam respons imun humoral maupun adaptif yang memiliki peranan patogenesis dalam berbagai kondisi autoimun termasuk IBD. Defisiensi vitamin D diketahui dapat mempengaruhi derajat aktivitas pada pasien dengan IBD. Beberapa studi menunjukkan terdapat peran vitamin D dalam meningkatkan angka remisi pada pasien dengan IBD. Namun studi lain menunjukkan tidak ada hubungan yang signifikan terhadap aktivitas klinis IBD dengan defisiensi vitamin D. Belum ada studi di Indonesia yang menilai hubungan kadar vitamin D dengan aktivitas klinis pada IBD.Tujuan. Mengetahui prevalensi defisiensi vitamin D pada pasien dengan IBD dan menilai perbedaan rerata kadar 25-OH D pada subjek dengan IBD aktif dengan remisi.Metode. Penelitian ini merupakan studi dengan desain potong lintang yang dilakukan di Rumah Sakit Cipto Mangunkusumo. Pasien dengan IBD yang datang ke Poliklinik Gastroenterologi dan dilakukan pemeriksaan kadar 25-OH-D. Subjek dengan kolitis ulseratif dinilai aktivitas klinisnya dengan menggunakan instrumen Simple Clinical Colitis Activity Index (SCCAI) dimana nilai <2 dikategorikan sebagai remisi, sedangkan subjek dengan penyakit Crohn dinilai aktivitas klinisnya dengan menggunakan instrumen Crohn’s Disease Activity Index (CDAI) dengan nilai <150 dikategorikan sebagai remisi. Dilakukan analisis perbedaan rerata kadar 25-OH-D antara subjek remisi dibandingkan aktif baik pada subjek dengan kolitis ulseratif dan penyakit Crohn.Hasil. Sebanyak 76 subjek memenuhi kriteria inklusi dan eksklusi, 48 subjek termasuk ke dalam kolitis ulseratif dan 28 lainnya penyakit Crohn. Sebanyak 65,3% subjek perempuan dengan rerata usia subjek adalah 46,39 (SB 16,25). Prevalensi defisiensi vitamin D pada pasien IBD adalah sebesar 46,1% dengan 32,1% pada penyakit Crohn dan 54,2% pada kolitis ulseratif. Tidak didapatkan adanya perbedaan median yang signifikan antara subjek dengan penyakit Crohn pada remisi (20,7 (12,25 – 32,55) ng/ml) dan aktif (15,7 (12,03 – 28,6) ng/ml) (p = 0,832), maupun subjek dengan kolitis ulseratif pada remisi (26,05 (19,33 – 30,73) ng/ml) dan aktif (25,05 (14,43 – 33,37) ng/ml) (p = 0,301).Kesimpulan. Prevalensi defisiensi vitamin D pada IBD adalah sebesar 46,1%. Tidak terdapat adanya perbedaan yang signifikan terhadap kadar 25-OH-D pada pasien dengan IBD yang aktif dibandingkan dengan remisi.

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Background. Vitamin D is one of the regulatory components that play a role in humoral and adaptive immune responses that have a pathogenesis role in various autoimmune conditions including IBD. Vitamin D deficiency is known to affect activity levels in patients with IBD. Several studies have shown that there is a role for vitamin D in increasing remission rates in patients with IBD. However, other studies have shown that there is no significant relationship between clinical activity of IBD and vitamin D deficiency. There are no studies in Indonesia that have assessed the relationship between vitamin D levels and clinical activity in IBD.

Aim. To determine the prevalence of vitamin D deficiency in patients with IBD and to assess the difference in mean 25-OH D levels in subjects with clinically active and remission.

Method. This is a cross-sectional study conducted at Cipto Mangunkusumo Hospital, Jakarta, Indonesia. Patients with IBD who came to the Gastroenterology Polyclinic and have their 25-OH-D levels checked. Subjects with ulcerative colitis were assessed for clinical activity using the Simple Clinical Colitis Activity Index (SCCAI) instrument where a value <2 was categorized as remission, while subjects with Crohn's disease were assessed for clinical activity using the Crohn's Disease Activity Index (CDAI) instrument with a value <150 categorized as remission. An analysis of the difference in mean 25-OH-D levels between remission versus active subjects was performed both in subjects with ulcerative colitis and Crohn's disease.

Results. A total of 76 subjects met the inclusion and exclusion criteria, 48 subjects had ulcerative colitis and 28 had Crohn's disease. A total of 65,3% of female subjects with the mean age of the subject was 46,39 (SB 16,25). The prevalence of vitamin D deficiency in IBD patients was 46,1% with 32,1% in Crohn's disease and 54,2% in ulcerative colitis. There was no significant median difference between subjects with Crohn's disease in remission (20,7 (12,25 – 32,55) ng/ml) and active (15,7 (12,03 – 28,6) ng/ml) (p = 0,832), as well as subjects with ulcerative colitis in remission (26,05 (19,33 – 30,73) ng/ml) and active (25,05 (14,43 – 33,37) ng/ml) (p = 0,301).

Conclusion. Prevalence of vitamin D deficiency in IBD is 46,1%. There was no significant difference in 25-OH-D levels in patients with active IBD compared with remission."

"Inflammatory bowel disease (IBD) merupakan penyakit kronis saluran cerna dengan siklus eksaserbasi-remisi. Masih terdapat tantangan dalam mempertahankan remisi dan menunda flare pada pasien IBD. Asupan gizi tertentu dapat memodifikasi mediator inflamasi pada saluran gastrointestinal sementara aktivitas fisik dapat mempengaruhi kadar sitokin sehingga keduanya dapat mempengaruhi perjalanan IBD. Penelitian ini bertujuan untuk menganalisis hubungan antara potensi inflamasi diet dan aktivitas fisik dengan aktivitas penyakit IBD.Metode: Penelitian ini menggunakan desain potong lintang pada pasien IBD yang melakukan kontrol di Poliklinik Gastroenterologi Rumah Sakit Cipto Mangunkusumo (RSCM) selama periode Juli–September 2022. Pengambilan data mengenai potensi inflamasi diet berdasarkan skor Dietary Inflammatory Index (DII) dan aktivitas fisik berdasarkan skor International Physical Activity Questionnaire (IPAQ). Derajat aktivitas penyakit IBD diperoleh berdasarkan kuesioner Indeks Harvey-Bradshaw (HBI) untuk Penyakit Crohn (PC) dan Simple Colitis Clinical Activity Index (SCCAI) untuk Kolitis Ulseratif (KU). Analisis statistik dengan menggunakan uji KruskalWallis, Spearman, dan Regresi linear multipel.Hasil: Sebanyak 100 subjek penelitian didapatkan rerata skor DII pada kelompok PC adalah 0,22± 2,20 dengan tren rerata yang meningkat signifikan seiring dengan keparahan PC: -0,13 ± 2,3 (remisi), 0,17 ± 2,51 (ringan), 0,65 ± 2,11 (sedang), 0,68 ± 1,60 (berat); p=0,02. Rerata skor DII pada kelompok KU adalah 0,11 ± 2,45 dan tidak ditemukan perbedaan bermakna antar subgrup keparahan. Rerata skor aktivitas fisik pada kelompok PC dan KU berturut-turut adalah 5097,4 ± 2955,7 dan 6023,7 ± 4869,4. Tidak ditemukan perbedaan bermakna antara tingkat aktivitas fisik dan derajat aktivitas penyakit IBD. Skor DII secara independen dapat mempengaruhi aktivitas penyakit PC dari analisis multivariat (koefisien Î² 0,370; p= 0,006). Kesimpulan: Terdapat hubungan signifikan antara potensi inflamasi diet dengan derajat aktivitas penyakit PC. Tidak terdapat hubungan antara potensi inflamasi diet dengan derajat aktivitas penyakit KU maupun antara aktivitas fisik dengan derajat aktivitas penyakit IBD.

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Background: inflammatory bowel disease (IBD) is a chronic gastrointestinal disease with exacerbation-remission cycles. There are still challenges in maintaining remission and preventing flares in IBD patients. Intake of certain nutrients can modify inflammatory mediators of the gastrointestinal tract while physical activity may affect cytokine levels, therefore both can influence the course of  IBD. This study aims to analyze the association between inflammatory potential of diet and physical activity with IBD disease activity.

Method: in this cross-sectional study, IBD patients who had regular control at the gastroenterology outpatient clinic of RSCM were recruited during the period of July–September 2022. The data of inflammatory potential of diet obtained through the dietary Inflammatory Index (DII) score and physical activity data obtained through the International Physical Activity Questionnaire (IPAQ) score. The degree of IBD disease activity based on the Harvey-Bradshaw Index (HBI) for Crohn’s Disease (CD) and the Simple Colitis Clinical Activity Index (SCCAI) for Ulcerative Colitis (UC). Statistical analysis using the Kruskal-Wallis test, Spearman test, and Multiple Linear Regression test.

Results: A total of 100 subjects obtained the mean DII score in the CD group was 0.22± 2.20 with an upward trend that increased significantly as CD disease severity progressed: -0.13 ± 2.3 (remission), 0.17 ± 2.51 (mild), 0.65 ± 2.11 (moderate), 0.68 ± 1.60 (severe); p=0,02. The mean DII score in the UC group was 0.11 ± 2.45 and there was no significant difference among severity subgroups. The mean physical activity scores in the CD and UC groups were 5097.4± 2955.7 and 6023.7 ± 4869.4 respectively. There was no significant difference of physical activity among various degrees of IBD severity. DII scores independently influenced CD disease activity based on multivariate analysis (β-coefficient 0.370; p= 0.006).

Conclusion: A significant association between the inflammatory potential of diet and CD disease activity was observed. There was no association between inflammatory potential of diet and UC disease activity, as well as between physical activity and IBD disease activity."

"Latar Belakang. Penyakit radang usus atau Inflammatory Bowel Disease (IBD) memiliki gejala gangguan saluran pencernaan yang tidak dapat diprediksi, tidak menyenangkan, dan kerap kali menimbulkan rasa malu bagi penderitanya. Berbagai ketidaknyamanan tersebut dapat mempengaruhi penurunan kualitas hidup pasien IBD hingga meningkatkan morbiditas dan mortalitas di masa depan. Perlu instrumen yang sahih dan andal untuk menilai kualitas hidup pasien dengan IBD.Tujuan. Penelitian ini bertujuan untuk mengetahui keandalan dan kesahihan Inflammatory Bowel Disease Questionnaires-9 (IBDQ-9) versi bahasa Indonesia untuk menilai kualitas hidup pasien dengan IBD.Metode. Instrumen asli IBDQ-9 diterjemahkan ke bahasa Indonesia dan diterjemahkan kembali ke bahasa Inggris lalu dikonfirmasi kepada pemilik instrumen. Kemudian dilakukan uji kesahihan isi dengan Content Validity Index (CVI). Studi potong lintang dengan populasi terjangkau pasien dewasa IBD di Poliklinik Gastroenterologi, Rumah Sakit Umum Pusat Nasional Cipto Mangunkusumo Jakarta pada bulan November 2022 yang berusia 18-59 tahun, telah mengalami IBD minimal 2 minggu dan bersedia untuk menandatanganiinformed consent sebagai responden penelitian. Perbandingan skor total IBDQ-9 dengan SF-36 versi Indonesia dinilai dengan uji korelasi Spearman lalu uji keandalan dengan menentukan alfa Cronbach dan Intraclass Correlation Coefficient (ICC).Hasil. Sebanyak 124 pasien IBD dianalisis dengan uji Spearman menunjukkan korelasi yang tinggi dan signifikan antara IBDQ-9 dengan SF-36 (r=0,769 dan p<0,001). IBDQ-9 versi bahasa Indonesia memiliki nilai alfa Cronbach versi bahasa Indonesia sebesar 0,883 dan nilai ICC yang baik juga sebesar 0,883 (IK95% 0,849-0,912).Kesimpulan. Instrumen IBDQ-9 versi Bahasa Indonesia sahih dan andal untuk menilai kualitas hidup pasien dengan IBD di Indonesia.

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Latar Belakang. Penyakit radang usus atau Inflammatory Bowel Disease (IBD) memiliki gejala gangguan saluran pencernaan yang tidak dapat diprediksi, tidak menyenangkan, dan kerap kali menimbulkan rasa malu bagi penderitanya. Berbagai ketidaknyamanan tersebut dapat mempengaruhi penurunan kualitas hidup pasien IBD hingga meningkatkan morbiditas dan mortalitas di masa depan. Perlu instrumen yang sahih dan andal untuk menilai kualitas hidup pasien dengan IBD.

Tujuan. Penelitian ini bertujuan untuk mengetahui keandalan dan kesahihan Inflammatory Bowel Disease Questionnaires-9 (IBDQ-9) versi bahasa Indonesia untuk menilai kualitas hidup pasien dengan IBD.

Metode. Instrumen asli IBDQ-9 diterjemahkan ke bahasa Indonesia dan diterjemahkan kembali ke bahasa Inggris lalu dikonfirmasi kepada pemilik instrumen. Kemudian dilakukan uji kesahihan isi dengan Content Validity Index (CVI). Studi potong lintang dengan populasi terjangkau pasien dewasa IBD di Poliklinik Gastroenterologi, Rumah Sakit Umum Pusat Nasional Cipto Mangunkusumo Jakarta pada bulan November 2022 yang berusia 18-59 tahun, telah mengalami IBD minimal 2 minggu dan bersedia untuk menandatangani

informed consent sebagai responden penelitian. Perbandingan skor total IBDQ-9 dengan SF-36 versi Indonesia dinilai dengan uji korelasi Spearman lalu uji keandalan dengan menentukan alfa Cronbach dan Intraclass Correlation Coefficient (ICC).

Hasil. Sebanyak 124 pasien IBD dianalisis dengan uji Spearman menunjukkan korelasi yang tinggi dan signifikan antara IBDQ-9 dengan SF-36 (r=0,769 dan p<0,001). IBDQ-9 versi bahasa Indonesia memiliki nilai alfa Cronbach versi bahasa Indonesia sebesar 0,883 dan nilai ICC yang baik juga sebesar 0,883 (IK95% 0,849-0,912).

Kesimpulan. Instrumen IBDQ-9 versi Bahasa Indonesia sahih dan andal untuk menilai kualitas hidup pasien dengan IBD di Indonesia."