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By TARIK ZAHER , MD Assistant professor of Tropical Medicine , Zagazig University ,Egypt In general, there has been a distinct northsouth gradient in risk. In North America, incidence rates range from 6.0 to 15.6 cases per 100,000 person-years. In contrast, studies have reported significantly lower incidence rates of 0.6 to 6 per 100,000 person-years in other parts of the world, including Asia, Africa, and Latin America. The etiology of UC is currently unknown but is likely multifactorial ; complex interaction of three elements: genetic susceptibility, host immunity, and environmental factors. Family history is one of the most important risk factors for developing the disease. There are susceptibility genes for UC on chromosomes 1, 2, 3, 5, 6, 7, 10, 12, and 17. The C3435T polymorphism for the human multidrug resistance 1 (MDR1) gene is linked to susceptibility for UC . Several centers have reported an association between severe disease and a rare allele of HLA-DR1 (DRB1*0103). Several infectious organisms, including mycobacteria and viruses, have been implicated in the pathogenesis of IBD. Three studies have identified more than 45,000 bacterial small-subunit (SSU) rRNA genes in UC patients. A breakdown in the balance between protective and harmful intestinal bacteria, termed dysbiosis, can lead to disease. Smoking ,intestinal parasites and appendectomy are protective. Breaches in the well-regulated mucosal immune system lead to the chronic, uncontrolled mucosal inflammation observed in UC(increase TH1). The concept that UC is an autoimmune disease is supported by its increased association with other autoimmune disorders, including thyroid disease, diabetes mellitus, and pernicious anemia. Studies have suggested that pANCA may be associated with a more-aggressive disease course. A novel T-cell–mediated inflammatory pathway, which appears to be involved in the pathogenesis of both Crohn's disease and UC, has been discovered and centers on the Th17 cell lineage. Th17 cells have been shown to produce a variety of cytokines, most notably IL-6 and IL-17. IL-17 is a potent proinflammatory cytokine that not only facilitates T-cell activation but also stimulates a variety of cells. 45% of patients with UC have disease limited to the rectosigmoid, 35% have disease extending beyond the sigmoid but not involving the entire colon, and 20% of patients have pancolitis. The mucosa in UC appears hyperemic, edematous, and granular in mild disease. As disease progresses, the mucosa becomes hemorrhagic, with visible punctate ulcers. These ulcers can enlarge and extend into the lamina propria. Epithelial regeneration with recurrent attacks results in the formation of pseudopolyps. Another characteristic appearance of longstanding disease is atrophic and featureless colonic mucosa. Neutrophilic infiltration of colonic crypts gives rise to cryptitis and ultimately to crypt abscesses with neutrophilic accumulations in crypt lumens. This migration of neutrophils from the circulation into the lamina propria occurs in response to a variety of chemoattractants, including chemotactic peptides of colonic bacteria, IL-8, activated complement, plateletactivating factor, and leukotriene B4. Chronic inflammatory infiltrate. Inflammation in UC characteristically is confined to the mucosa. Following the initial flare, 40% to 65% of patients have an intermittent course, and 5% to 10% of patients have a chronic continuous course. Up to 10% of patients have a severe first attack ultimately requiring colectomy. Common symptoms include diarrhea, rectal bleeding, passage of mucus, tenesmus, urgency, and abdominal pain. In more-severe cases, fever and weight loss may be prominent. Patients with mild or even moderately severe disease exhibit few abnormal physical signs. Patients with severe attacks also might appear well, but most are ill with tachycardia, fever, orthostasis, and weight loss. In fulminant colitis, the abdomen often becomes distended and firm, with absent bowel sounds and signs of peritoneal inflammation. There may be aphthoid ulceration of the oral mucosa. Clubbing of the fingernails is a manifestation of chronic disease. Peripheral edema can occur secondary to hypoalbuminemia. Signs of extraintestinal manifestations Hematologic changes, including anemia, leukocytosis, and thrombocytosis, reflect active disease. Iron deficiency anemia may be present because of chronic blood loss. Anemia also may be present secondary to bone marrow suppression resulting from chronic inflammation or medications, including azathioprine, 6mercaptopurine (6-MP), and sulfasalazine. Serum inflammatory markers including erythrocyte sedimentation rate (ESR) and Creactive protein (CRP) may be elevated in active disease. Colonoscopy is not recommended in patients with severely active disease for fear of perforation; care must be taken to avoid excessive distention. A plain film can give considerable information with respect to the extent of disease. The presence of marked colonic dilatation suggests fulminant colitis or toxic megacolon. Barium enema provides information on their location, length, and diameter and allows visualization of the entire colon when the presence of strictures precludes advancement of the colonoscope. Mild <4 stools/day, without or with only small amounts of blood No fever No tachycardia Mild anemia ESR < 30 mm/hr Moderate Intermediate between mild and severe Severe >6 stools/day, with blood Fever > 37.5°C Heart rate > 90 beats/min Anemia with hemoglobin level < 75% of normal ESR > 30 mm/hr The goals of therapy of UC are to induce remission, to maintain remission, to maintain adequate nutrition, to minimize disease- and treatmentrelated complications, and to improve the patient's quality of life. Mild Disease 5-Aminosalicylates (Sulfasalazine , Olsalazine , Balsalazide , Mesalamine ):>2gm/d -Topical (distal colitis) -Oral (distal/extensive colitis) -Combination Moderate Disease 5-Aminosalicylates : -Topical (distal colitis) -Oral (distal/extensive colitis) - Combination Glucocorticoids: -Topical (distal colitis): -Oral (distal/extensive colitis): 1 mg/kg /day predinisolon -Combination Azathioprine or 6-mercaptopurine : 1 mg/kg /day Severe Disease IV glucocorticoids IV cyclosporine : 2 mg/kg/day(blood level 200 - 300 ng/ml) IV infliximab: 5 mg/kg/day ; 0,2,6 weeks 5-Aminosalicylates -Topical (distal colitis) -Oral (distal/extensive colitis):1.5 gm /day Azathioprine or 6mercaptopurine:1mg/kg/day Infliximab:5mg/kg every 2 monthes Dose-Related Alopecia Anorexia Back pain Folate malabsorption (with sulfasalazine) Headache Nausea, vomiting, dyspepsia Non–Dose-Related Agranulocytosis, aplastic anemia Arthralgia Colitis Fever Fibrosing alveolitis, pulmonary eosinophilia Hemolytic anemia (Heinz bodies) Hepatitis Hypersensitivity skin rashes (occasionally with photosensitivity) Male infertility (with sulfasalazine) Pancreatitis Pericarditis, myocarditis Acne Impaired wound healing Purpura, ecchymoses, petechiae Striae Adrenal insufficiency Cushingoid appearance Dyspepsia Dysphagia/odynophagia (candidiasis) Numerous pathogens Growth retardation Hyperglycemia, secondary diabetes mellitus Hyperlipidemia, altered fat distribution Hypertension Myopathy Osteonecrosis Osteoporosis Anxiety, mood swings Depression Insomnia Psychosis Cataracts Glaucoma Abnormal liver biochemical test results Bone marrow suppression Hypersensitivity reactions (fever, rash, arthralgia) Infections Lymphoma Nausea, abdominal pain, diarrhea Pancreatitis Anaphylaxis Diarrhea Electrolyte abnormalities Gingival hyperplasia Headache Hepatotoxicity Hirsutism Hypertension Infections Nausea, vomiting Opportunistic infections Paresthesia Renal insufficiency Seizure Tremor Prophylaxis against Pneumocystis pneumonia (PCP) during therapy is required. Antibiotics(metronidazole, ciprofloxacine, refaximin). Probiotics (Lactobacillus or Bifidobacterium), Prebiotics(food constituents increasing, probiotics and Synbiotics( both). Nicotine patches. Heparin: anti-inflammatory. Biological Therapy: -Anti-Tumor Necrosis Factor Antibodies: infliximab and adalimumab -Anti-Adhesion Molecules: Alicaforsen Cytapheresis: decrease WBCs. Peroxisome Proliferator Receptor Agonists(rosiglitazon) Budesonide-MMX : decrease the rate of steroid side effects. Tofacitinib:oral Janus kinase 3 (JAK3) inhibitor Fish oil: protecting the integrity of colonic mucosa Trichuris suis : increase TH2. Daclizumab : humanized monoclonal antibody against the IL-2 receptor . 1- Risk of infection Serious infections have happened in patients Receiving TNFblocking; infections include tuberculosis (TB) and infections caused by viruses, fungi or bacteria that have spread throughout the body. 2- Risk of Cancer There have been cases of unusual cancers(lymphomas) in children and teenage patients using TNFblocking agents. Indications for Surgery in Patients with Ulcerative Colitis -Colonic dysplasia or carcinoma -Colonic hemorrhage, uncontrollable -Colonic perforation -Growth retardation -Intolerable or unacceptable side effects of medical therapy -Medically refractory disease -Systemic complications that are recurrent or unmanageable -Toxic megacolon Acute colonic dilatation with a transverse colon diameter of greater than 6 cm (on radiologic examination) and loss of haustration in a patient with a severe attack of colitis. Colonic strictures complicate UC in approximately 5% of patients, most commonly in those with extensive and longstanding colitis. Patients with colonic strictures usually present with alterations in bowel habits, both constipation and diarrhea. One series reported malignancy in 24% of colonic strictures in patients with UC. In general, the risk of colorectal cancer may be estimated to increase within the range of 0.5% to 1.0% per year after 8 to 10 years of disease in patients with extensive UC. Surveillance by colonoscopy every year after 8 years of UC ( biopsy every 10 cm). Pouchitis is said to occur when there is nonspecific inflammation of the ileal reservoir, resulting in variable clinical symptoms resembling those of UC. The mainstay of therapy for pouchitis is antibiotics. Angular stomatitis Aphthous stomatitis Erythema nodosum Oral ulcerations Psoriasis Pyoderma gangrenosum Pyostomatitis vegetans Sweet's syndrome (acute febrile neutrophilic dermatosis) Conjunctivitis Episcleritis Retinal vascular disease Scleritis Uveitis, iritis Ankylosing spondylitis Osteomalacia Osteonecrosis Osteopenia Osteoporosis Peripheral arthropathy Sacroiliitis Autoimmune hepatitis Cholangiocarcinoma Pericholangitis Primary sclerosing cholangitis Hepatic steatosis Anemia of chronic disease Autoimmune hemolytic anemia Hypercoagulable state Iron deficiency anemia Leukocytosis or thrombocytosis Leukopenia or thrombocytopenia