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"Latar belakang dan tujuan: Morbiditas dan mortalitas pascaCABG salah satunya dipengaruhi respon inflamasi oleh penggunaan mesin CPB. Di beberapa pusat, sering dilakukan pemberian kortikosteroid untuk menurunkan respon inflamasi. Terdapat berbagai uji klinis yang memberikan hasil yang masih kontroversial. Deksametason dipilih karena memiliki potensi efek glukokortikoid yang tinggi, tanpa efek mineralokortikoid, masa kerja yang panjang, relatif aman bagi pasien, serta mudah untuk didapat. Penelitian ini bertujuan untuk mengetahui apakah penggunaan deksametason lebih efektif untuk memperbaiki keluaran klinis dan mengendalikan penanda inflamasi jika dibandingkan plasebo pada pasien yang menjalani operasi CABG on pump. Metode: Randomisasi 60 sampel menjadi grup deksametason (n=30) dan grup plasebo (n=30). Variabel dengan sebaran normal dilakukan analisis statistik independent t-test, sedangkan data dengan sebaran tidak normal dilakukan analisis statistik nonparametrik yaitu Mann-Whitney test. Analisis univariat antara dua kelompok studi akan dilakukan menggunakan uji fisher exact test. Hasil: Uji statistik kejadian MACE dengan grup deksametason dibandingkan grup plasebo, didapatkan nilai RR 1,389 dengan CI 0,995-1,938 (p =0,045). Deksametason memiliki keunggulan yang dapat dilihat dari parameter durasi ventilasi mekanik (deksametason 7 (5-14) vs plasebo 10 (5-19), p <0,0001), lama rawat ICU (deksametason 16 (11-22) vs plasebo 18 (12-72), p =0,017), lama rawat rumah sakit (deksametason 5 (5-7) vs plasebo 6 (5-15), p = 0,005), penanda inflamasi IL-6 (deksametason 114 (32-310) vs plasebo 398 (72-1717), p <0,0001) dan PCT (deksametason 1,08 (0,31-3,8) vs plasebo 3,7 (1,06-11,4), p <0,0001). Simpulan: Pemberian deksametason efektif memperbaiki keluaran klinis, dan mengendalikan penanda inflamasi pascaoperasi dibandingkan plasebo.

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Background and purpose: Mortality and morbidity post CABG are affected by inflammatory response which are caused by usage of CPB machine. In some centre, corticosteroid are often used to reduce inflammatory response. There are various clinical trials that provide controversial results. Dexamethasone was chosen because it has a high potential for glucocorticoid effects, without mineralocorticoid effects, long working period, relatively safe for patients, and easy to obtain. This study aims to determine whether the use of dexamethasone is more effective in improving clinical outcomes and controlling inflammatory markers when compared to placebo in patients undergoing on pump CABG.

Methods: 60 sample are randomized into dexamethasone group (n=30) and placebo group (n=30). Variables with normal distribution were carried out independent t-test statistical analysis, whereas data with abnormal distribution were analyzed using nonparametric statistics, namely Mann-Whitney test. Univariate analysis between the two study groups will be conducted using the fisher exact test.

Result: The incidence of MACE with the dexamethasone group compared to the placebo group was obtained RR 1,389 with CI 0,995-1,938 (p =0,045). Dexamethasone has advantages that can be seen from the parameters of duration of mechanical ventilation (dexamethasone 7 (5-14) vs placebo 10 (5-19), p <0,0001). ICU stay (dexamethasone 16 (11-22) vs placebo 18 (12-72), p =0,017), hospital stay (dexamethasone 5 (5-7) vs placebo 6 (5-15), p = 0,005), IL-6 (dexamethasone 114 (32-310) vs placebo 398 (72-1717), p <0,0001) and PCT (dexamethasone 1,08 (0,31-3,8) vs placebo 3,7 (1,06-11,4), p <0,0001).

Conclusion: The administration of dexamethasone improves clinical output, and managed to controls post operative inflammatory marker more effectively compared to placebo."

"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."

"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."

"Latar belakang: Berdasarkan pilot study di divisi Bedah Jantung Dewasa Rumah Sakit Pusat Jantung dan Pembuluh Darah Harapan Kita, SIRS lebih sering terjadi pada OPCAB dibandingkan dengan on-pump CABG, 67% vs 33% (30 sampel, 2017). Berangkat dari hal tersebut, peneliti melakukan uji klinis memberikan deksametason pada pasien yang menjalani operasi OPCAB. Metode: Pengumpulan sampel dilakukan secara konsekutif di divisi Bedah Jantung Dewasa Rumah Sakit Pusat Jantung dan Pembuluh Darah Harapan Kita antara Agustus 2018 - Januari 2019. Sampel yang memenuhi kriteria inklusi dan eksklusi dirandomisasi menjadi grup deksametason (n=30) dan grup plasebo (n=30). Intervensi deksametason intravena dosis 1 mg/KgBB (maksimal 100 mg) atau plasebo menggunakan normal salin (NaCl 0,9%). Analisis statistik digunakan independent t-test, Mann-Whitney test, fisher exact test dan AUC. Hasil: Insiden MACE pada grup deksametason dibandingkan grup plasebo (RR 0,385, CI 95%: 0,157-0,945, p = 0,024). Keluaran klinis lebih baik ditemukan pada grup deksametason dibandingkan grup plasebo untuk durasi ventilasi mekanik (6 (5-16) jam vs 8 (5-72) jam, p = 0,029), lama rawat ICU (17,5 (12-32) jam vs 19 (13-168) jam, p = 0,028), lama rawat rumah sakit (5 (5-8) hari vs 6,5 (5-30) hari, p = 0,04) dan VIS (0 (0-15) vs 5 (0-100), p = 0,045). Hasil penanda inflamasi, terdapat perbedaan rata-rata yang bermakna antara grup deksametason dibandingkan grup plasebo pada IL-6 (217,4 pg/mL, CI 95%: 107,9-326,8, p = 0,0001), PCT (3,41 µg/L, CI 95%: 2,1-4,71, p = 0,0001) dan CRP (52,3 mg/L, CI 95%: 28.8-75,8, p = 0,0001). Pada analisis AUC terdapat hubungan signifikan antara penanda inflamasi dengan insiden MACE pada IL-6 (AUC 0,728, CI 95%: 0,585-0,871, p = 0,005) dan PCT (AUC 0,723, CI 95%: 0,578-0,868, p = 0,007). Kesimpulan: Pemberian deksametason praoperasi OPCAB, efektif memperbaiki keluaran klinis dan mengendalikan reaksi inflamasi pascaoperasi dibandingkan plasebo.

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Background: Based on a pilot study in the Adult Heart Surgery division of Harapan Kita Heart and Vascular Center Hospital, SIRS is more common in OPCAB compared to on-pump CABG, 67% vs 33% (30 samples, 2017). Based from this result, this research conducted a clinical trial to provide dexamethasone in patients undergoing OPCAB surgery. Methods: Samples were collected consecutively in the Adult Heart Surgery division of Harapan Kita Heart and Vascular Center Hospital between August 2018 - January 2019. Samples that fulfill inclusion and exclusion criteria were randomized to dexamethasone group (n=30) and placebo group (n=30). Intervention using intravenous dexamethasone dose of 1 mg/KgBB (maximum 100 mg) or placebo using normal saline (0.9% NaCl). Statistical analysis were used independent t-test, Mann-Whitney test, fisher exact test and AUC. Results: MACE incidence in dexamethasone group compared to placebo group (RR 0.385, 95% CI: 0.157-0.945, p = 0.024). Clinical output of dexamethasone group was better than placebo group in duration of mechanical ventilation (6 (5-16) hours vs 8 (5-72 ) hours, p = 0.029), ICU length of stay (17.5 (12-32) hours vs 19 (13-168) hours, p = 0.028), hospital length of stay (5 (5-8) days vs 6.5 (5-30) days, p = 0.04) and VIS (0 (0-15) vs 5 (0-100), p = 0.045). As a result of the inflammatory markers, there was a significant average difference between dexamethasone group compared to the placebo group in IL-6 (217.4 pg/mL, 95% CI: 107.9-326.8, p = 0,0001), PCT ( 3.41 µg/L, 95% CI: 2.1-4.71, p = 0.0001) and CRP (52.3 mg/L, 95% CI: 28.8-75.8, p = 0.0001 ) In the AUC analysis there was a significant association between inflammatory markers with the incidence of MACE in IL-6 (AUC 0.728, 95% CI: 0.585-0.871, p = 0.005) and PCT (AUC 0.723, 95% CI: 0.578-0.868, p = 0.007). Conclusion: Preoperative dexamethasone OPCAB is effective to improving clinical output and controlling postoperative inflammatory reactions compared to placebo."

"ABSTRACTThree types of cyclopentanone derivatives have been synthesized from aromatic aldehyde and ketone derivatives undera base condition through aldol condensation. These cyclopentanone products were 2,5-dibenzylidene-cyclopentanone (a), 2,5-bis-(4-hydroxy-benzylidene)-cyclopentanone (b),and 2,5-bis-(4-hydroxy-benzylidene)-cyclopentanone (c)which has a yield of 63-99%. The chemical structure of these compounds were determined using UV, IR and NMRspectroscopy. In order to clarify the role of hydroxyl and amine moieties, toxic, antioxidant and anti-inflammatoryactivities were carried out. The toxic test indicated that thecompounds showed strong toxicity. In addition, the presenceof hydroxyl and amine groups on both rings of curcumin increased the antioxidant and anti-inflammatory activities."

"Indonesia merupakan negara dengan jumlah kasus TB tertinggi kedua di dunia dengan insidensi 354 per 100.000 penduduk dan 969.000 kasus pada tahun 2021. Salah satu pemeriksaan pada  TB yaitu dengan pemeriksaan darah seperti hitung jumlah leukosit. Peningkatan jumlah leukosit dan netrofil merupakan tanda reaksi inflamasi terutama bila disebabkan oleh infeksi bakteri. Mikronutrien seperti vitamin A dan seng berperan penting dalam pengobatan TB. Studi di Indonesia dan Ethiopia sebelumnya menunjukkan rendahnya asupan vitamin A dan seng serta sebagian besar mengalami defisiensi. Vitamin A dan metabolit aktifnya berperan dalam pertumbuhan dan diferensiasi sel, terutama sel epitel yang berhubungan dengan mukosa, limfosit T dan B, makrofag, dan pembentukan antibodi. Seng juga merupakan elemen penting dalam berbagai fungsi fisiologis dan metabolisme seperti menjaga integritas imunologis, imunitas seluler, dan aktivitas antioksidan. Saat ini, belum terdapat studi yang menghubungkan asupan vitamin A dan seng dengan penanda inflamasi dengan parameter NLR dan PLR pada pasien TB paru. Penelitian ini bertujuan untuk mengetahui hubungan asupan vitamin A dan seng dengan penanda inflamasi pada pasien TB paru di RSUP Persahabatan. Penelitian ini merupakan penelitian potong lintang. Sebanyak 133 subjek direkrut. Mayoritas subjek memiliki usia paling rendah 19 tahun dan paling tinggi 74 tahun. Sebagian besar subjek berjenis kelamin laki-laki, berada dalam jenjang pendidikan sedang (tamat SMA, tidak tamat perguruan tinggi), berpendapatan kurang dari UMP DKI Jakarta. Sebanyak 42,1 % memiliki berat badan normal. Sebagian besar subjek berada dalam fase pengobatan intensif, memiliki status bakteriologis BTA/TCM/kultur positif, tidak ada komorbid, dan tidak pernah merokok. Penelitian ini tidak menemukan adanya korelasi antara asupan vitamin A dan seng dengan nilai NLR dan PLR pada pasien tuberkulosis paru di RSUP Persahabatan.

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Indonesia is the country with the second highest number of TB cases in the world with an incidence of 354 per 100,000 population and 969,000 cases in 2021. One of the tests for TB is blood tests such as counting leukocytes. An increase in the number of leukocytes and neutrophils is a sign of an inflammatory reaction, especially if caused by a bacterial infection. Micronutrients such as vitamin A and zinc play an important role in TB treatment. Previous studies in Indonesia and Ethiopia showed low intakes of vitamin A and zinc and that most were deficient. Vitamin A and its active metabolites play a role in cell growth and differentiation, especially epithelial cells associated with mucosa, T and B lymphocytes, macrophages, and antibody formation. Zinc is also an important element in various physiological and metabolic functions such as maintaining immunological integrity, cellular immunity and antioxidant activity. Currently, there are no studies that link vitamin A and zinc intake with inflammatory markers with NLR and PLR parameters in pulmonary TB patients. This study aims to determine the relationship between vitamin A and zinc intake with inflammatory markers in pulmonary TB patients at Persahabatan Hospital. This research is a cross-sectional study. A total of 133 subjects were recruited. The majority of subjects had a minimum age of 19 years and a maximum of 74 years. Most of the subjects were male, had a moderate level of education (graduated from high school, not graduated from college), and earned less than the DKI Jakarta UMP. As many as 42.1% had normal body weight. Most of the subjects were in the intensive treatment phase, had positive BTA/TCM/culture bacteriological status, had no comorbidities, and had never smoked. This study did not find a correlation between vitamin A and zinc intake and NLR and PLR values ​​in pulmonary tuberculosis patients at Persahabatan Hospital."

"Tumor necrosis factor alpha (TNF-alpha) adalah salah satu sitokin proinflamasi yang berperan pada timbulnya cedera iskemia-reperfusi pasien infark miokard akut yang menjalani tindakan intervensi koroner perkutan primer (IKPP). Kolkisin merupakan salah satu obat antiinflamasi yang diduga memiliki pengaruh terhadap TNF-alpha. Penelitian ini bertujuan untuk mengetahui peran kolkisin terhadap kadar TNF-alpha serum pasien infark miokard akut dengan tindakan intervensi koroner perkutan primer. Desain penelitian uji klinis acak tersamar ganda menggunakan sampel sisa serum penelitian dari subjek pasien infark miokard akut Rumah Sakit dr. Cipto Mangunkusumo. Subjek penelitian dibagi menjadi dua kelompok. Kelompok studi diberikan loading dose kolkisin 2 mg, kemudian dilanjutkan 2 x 0,5 mg per hari secara oral selama 48 jam, sementara kelompok kontrol diberikan plasebo. Analisis kadar TNF-alpha menggunakan metode ELISA yang diperiksa sebelum dan 48 jam pasca-IKPP untuk mendapatkan delta perubahan kadar TNF-alpha. Terdapat 64 subjek yang dianalisis terdiri dari 30 kelompok kontrol dan 34 kelompok studi. Delta kadar TNF-alpha pasca-IKPP kelompok kontrol (2,2) terhadap delta kadar TNF-alpha kelompok studi (0,7). Penelitian ini merupakan penelitian pertama tentang pengaruh kolkisin terhadap kadar TNF-alpha pada pasien infark miokard akut dengan tindakan intervensi koroner perkutan primer di Indonesia. Pengukuran TNF-alpha perlu dilakukan lebih dari dua kali untuk melihat dinamika kadar TNF-alpha pada pasien infark miokard akut yang menjalani tindakan intervensi koroner perkutan primer dan penelitian lanjutan diperlukan untuk menilai peran kolkisin sebagai obat antiinflamasi dengan pemeriksaan menggunakan metoda ELISA dengan reagen high-sensitive.

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Tumor necrosis factor alpha (TNF-alpha) is a proinflammatory cytokine that plays a role in the emergence of ischemia-reperfusion injury in patients with acute myocardial infarction undergoing primary percutaneous coronary intervention (PCI). Colchicine is an anti-inflammatory drug believed to affect TNF-alpha. This study aimed to determine the role of colchicine on serum TNF-alpha levels in acute myocardial infarct patients undergoing primary percutaneous coronary intervention. The research design was a double-blind, randomized clinical trial using residual research serum samples from patients with acute myocardial infarction at Dr. Hospital. Cipto Mangunkusumo. The research subjects were divided into two groups. The study group was given a loading dose of 2 mg colchicine and then continued at 2 x 0.5 mg per day orally for 48 hours, whereas the control group was given a placebo. Analysis of TNF-alpha levels using the ELISA method was performed before and 48 hours after primary percutaneous coronary intervention to obtain the delta of changes in TNF-alpha levels. There were 64 subjects analyzed, comprising 30 control groups and 34 study groups. The delta of TNF-alpha levels post-PCI in the control group (2.2) compared with the delta of TNF-alpha levels in the study group (0.7). This is the first study on the effect of colchicine on TNF-alpha levels in acute myocardial infarction patients with primary percutaneous coronary intervention in Indonesia. TNF-alpha measurements need to be carried out more than twice to determine the dynamics of TNF-alpha levels in patients with acute myocardial infarction undergoing primary percutaneous coronary intervention, and further research is needed to assess the role of colchicine as an anti-inflammatory drug by ELISA with high-sensitive reagents."

"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."