Other gastrointestinal disorders like Whipple's disease, celiac disease, and intestinal bypass surgery for severe obesity can also cause joint involvement. The pathogenesis of arthritis in these conditions is likely influenced by immunologic, genetic, and abnormal bowel permeability factors, though the precise mechanisms are still unknown.[4]
Signs and symptoms
Historically, there have been two main patterns of joint involvement with enteropathic arthritis: axial involvement, which includes sacroiliitis with or without spondylitis resembling idiopathic ankylosing spondylitis, and peripheral arthritis.[4] Additional conditions that may manifest are enthesopathy, tendinitis, and a variety of other conditions such as periostitis, clubbing, and granulomatous lesions of the bone and joint.[6]
Two types of peripheral arthritis have been identified. Pauciarticular arthritis, or type I, usually affects fewer than five major weight-bearing joints. It usually has an asymmetrical pattern and is linked to active bowel disease; monoarthritis isn't uncommon. Both big and small joints are affected, mainly lower limb joints like the metatarsophalangeal joints, ankles, and knees. Shoulder and hip arthritis is less common and is typically linked to spondylitis and sacroiliitis.[7] It does not cause joint deformities, but it is typically migratory, transitory, and recurrent.[8] Joint symptoms, particularly in Crohn's disease, can manifest before bowel symptoms do. In ulcerative colitis, the time of the initial arthritis attack appears to be unrelated to the length of the colitis. Furthermore, a relapse of peripheral arthritis is often associated with a flare-up of the gut symptoms, primarily in ulcerative colitis.[7]
Polyarthritis type II primarily affects the small joints. Rarely does it come before an IBD diagnosis. It usually progresses on its own schedule apart from the bowel illness. Months may pass during an active synovitis episode, and it may recur frequently. Years may pass between periods of exacerbations and remissions.[7]
The spectrum of axial involvement includes true ankylosing spondylitis, which is characterized by classic clinical and radiologic features, as well as asymptomatic sacroiliitis and inflammatory pain in the lower back regardless of the radiological evidence of the condition. Axial involvement may occur years before bowel disease. Inflammatory low back pain, buttocks pain, and chest pain are the main complaints. Typically occurring before the age of 45, inflammatory back pain often begins slowly, is often unilateral, sporadic, and worsens while at rest. It can also be aggravated by coughing or sneezing, worsen in the morning, and cause fatigue. The pain persists for at least three months. Enthesitis of the manubriocostal, costosternal, and costovertebral articulations causes thoracic pain. It worsens with coughing and deep inspirations, and it restricts the expansion of the respiratory system with varying-length episodes. Ankylosing spondylitis has been linked with dactylitis. It is distinguished by tenosynovitis that affects the flexor tendons resulting in inflammatory swelling in one or more fingers or toes. One of the main indicators that the disease is progressing toward generalized ankylosis is the restriction of cervical spine mobility.[7]
Causes
It is unknown what exactly causes the enteropathic arthropathies. Increased permeability from GI tract inflammation can lead to the absorption of antigenic substances, such as bacterial antigens. The musculoskeletal tissues, such as entheses and the synovial membrane, may then localize these arthrogenic antigens, triggering an inflammatory response. Alternatively, by means of molecular mimicry, which involves the host's immune system reacting to these antigens in a cross-reaction with self-antigens present in the synovial membrane and other target organs, an autoimmune response may be triggered.[9]
In an effort to treat morbid obesity, small intestine bypass surgeries first emerged in the 1950s. The goal was to decrease the absorptive surface of the gut. In 20% to 80% of patients, postoperative arthritis-dermatitis syndrome and several metabolic side effects occur. When the jejunoileal bypass was used in place of the jejunocolonic bypass, similar problems still occurred.[23] Though mono- and oligoarthritis have also been reported, the typical clinical presentation is a migratory non-erosive seronegative polyarthritis affecting the ankles, wrists, shoulders, hands, and fingers.[24] Usually, the arthritis appears two to three years following the surgery.[25] Intestinal bypass arthritis has been linked to the overgrowth of bacteria in the blind loop segment of the bowel, and immunologic involvement appears likely due to the presence of immune complexes in the serum.[26] Reversing the bypass surgery is typically linked to a total and permanent remission of the arthritis, providing more proof of the connection between intestines and joint pathology.[24]
Diagnosis
No pathognomonic finding exists to support a diagnosis of IBD-related arthritis. In the appropriate clinical context, a suspicion of the diagnosis may arise. Radiographs of the pelvis and spine may reveal characteristic features of sacroiliitis and ankylosing spondylitis. The latter is usually bilateral, though reports have indicated a higher incidence of zygapophyseal jointankylosis and asymmetric sacroiliitis. Although erosive lesions, primarily of the metatarsal joints, are reported, radiographic changes are typically not associated with peripheral joint involvement. Certain characteristics of these lesions differ from those of rheumatoid arthritis, such as the absence of osteoporosis as well as the presence of neighboring bone proliferation. Occasionally, a damaging granulomatous synovitis linked to Crohn's disease may be observed. Radiographically, enteropathies are similar to those observed in other spondyloarthritis.[7]
Controlling intestinal inflammation is the primary treatment objective for peripheral arthritis, as the disease's activity frequently resembles that of bowel disease. For ulcerative colitis, sulfasalazine has been demonstrated to be beneficial in treating flare-ups as well as the underlying condition;[29] however, the picture for Crohn's disease is less clear. Sulfasalazine has been demonstrated to be beneficial in certain trials for Crohn's disease,[30] but not in others.[31]
^De Keyser F, Elewaut D, De Vos M, De Vlam K, Cuvelier C, Mielants H, Veys EM (November 1998). "Bowel inflammation and the spondyloarthropathies". Rheumatic Disease Clinics of North America. 24 (4). Elsevier BV: 785–813. doi:10.1016/s0889-857x(05)70042-9. PMID9891711.
^Wordsworth P (April 2000). "Arthritis and inflammatory bowel disease". Current Rheumatology Reports. 2 (2). Springer Science and Business Media LLC: 87–88. doi:10.1007/s11926-000-0045-3. PMID11123044. S2CID35543053.
^Adelizzi RA, Pecora AA, Chiesa JC (July 1982). "Celiac disease: case report with an associated arthropathy". The American Journal of Gastroenterology. 77 (7). Am J Gastroenterol: 481–485. PMID7091138.
^McDonagh JE, Griffiths ID (December 1992). "Arthritis--a presenting feature of occult coeliac disease". British Journal of Rheumatology. 31 (12): 857–858. doi:10.1093/rheumatology/31.12.857-a. PMID1458297.
^Collin P, Korpela M, Hällström O, Viander M, Keyriläinen O, Mäki M (1992). "Rheumatic complaints as a presenting symptom in patients with coeliac disease". Scandinavian Journal of Rheumatology. 21 (1). Informa UK Limited: 20–23. doi:10.3109/03009749209095057. PMID1570482.
^Mäki M, Hallström O, Verronen P, Reunala T, Lähdeaho ML, Holm K, Visakorpi JK (February 1988). "Reticulin antibody, arthritis, and coeliac disease in children". Lancet. 1 (8583). Elsevier BV: 479–480. doi:10.1016/s0140-6736(88)91280-9. PMID2893907. S2CID41488212.
^Chakravarty K, Scott DG (May 1992). "Oligoarthritis--a presenting feature of occult coeliac disease". British Journal of Rheumatology. 31 (5). Oxford University Press (OUP): 349–350. doi:10.1093/rheumatology/31.5.349. PMID1581779.
^Shagrin JW, Frame B, Duncan H (September 1971). "Polyarthritis in obese patients with intestinal bypass". Annals of Internal Medicine. 75 (3). American College of Physicians: 377–380. doi:10.7326/0003-4819-75-3-377. PMID5568149.
^Utsinger PD (June 1980). "Systemic immune complex disease following intestinal bypass surgery: bypass disease". Journal of the American Academy of Dermatology. 2 (6). Elsevier BV: 488–495. doi:10.1016/s0190-9622(80)80149-6. PMID6447168.
^Kaufmann HJ, Taubin HL (October 1987). "Nonsteroidal anti-inflammatory drugs activate quiescent inflammatory bowel disease". Annals of Internal Medicine. 107 (4). American College of Physicians: 513–516. doi:10.7326/0003-4819-107-4-513. PMID3498419.
^Wenckert A, Kristensen M, Eklund AE, Barany F, Jarnum S, Worning H, et al. (1978). "The long-term prophylactic effect of salazosulphapyridine (Salazopyrin) in primarily resected patients with Crohn's disease. A controlled double-blind trial". Scandinavian Journal of Gastroenterology. 13 (2). Informa UK Limited: 161–167. doi:10.3109/00365527809181743. PMID24891.
^Mease PJ, Goffe BS, Metz J, VanderStoep A, Finck B, Burge DJ (July 2000). "Etanercept in the treatment of psoriatic arthritis and psoriasis: a randomised trial". Lancet. 356 (9227). Elsevier BV: 385–390. doi:10.1016/s0140-6736(00)02530-7. PMID10972371. S2CID9392760.
^Marzo-Ortega H, McGonagle D, O'Connor P, Emery P (September 2001). "Efficacy of etanercept in the treatment of the entheseal pathology in resistant spondylarthropathy: a clinical and magnetic resonance imaging study". Arthritis and Rheumatism. 44 (9): 2112–2117. doi:10.1002/1529-0131(200109)44:9<2112::AID-ART363>3.0.CO;2-H. PMID11592375.
^Brandt J, Haibel H, Cornely D, Golder W, Gonzalez J, Reddig J, et al. (June 2000). "Successful treatment of active ankylosing spondylitis with the anti-tumor necrosis factor alpha monoclonal antibody infliximab". Arthritis and Rheumatism. 43 (6): 1346–1352. doi:10.1002/1529-0131(200006)43:6<1346::AID-ANR18>3.0.CO;2-E. PMID10857793.
^Van den Bosch F, Kruithof E, De Vos M, De Keyser F, Mielants H (November 2000). "Crohn's disease associated with spondyloarthropathy: effect of TNF-alpha blockade with infliximab on articular symptoms". Lancet. 356 (9244). Elsevier BV: 1821–1822. doi:10.1016/s0140-6736(00)03239-6. PMID11117919. S2CID1799909.
العلاقات البوسنية الغرينادية البوسنة والهرسك غرينادا البوسنة والهرسك غرينادا تعديل مصدري - تعديل العلاقات البوسنية الغرينادية هي العلاقات الثنائية التي تجمع بين البوسنة والهرسك وغرينادا.[1][2][3][4][5] مقارنة بين البلدين هذه مقارنة عامة و
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