{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,2]],"date-time":"2026-09-02T02:39:48Z","timestamp":1788316788682,"version":"build-2803163510"},"reference-count":23,"publisher":"Wiley","issue":"10","license":[{"start":{"date-parts":[[2021,8,24]],"date-time":"2021-08-24T00:00:00Z","timestamp":1629763200000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":["onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["Int J of Rheum Dis"],"published-print":{"date-parts":[[2021,10]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:sec><jats:title>Background<\/jats:title><jats:p>Parenchymal neuro\u2010Beh\u00e7et\u2019s disease involvement is the most serious complication of Beh\u00e7et's disease, and no sufficient data on its treatment exists. This study aims to investigate the efficacy and safety of infliximab treatment in neuro\u2010Beh\u00e7et\u2019s disease patients with parenchymal involvement.<\/jats:p><\/jats:sec><jats:sec><jats:title>Materials and Methods<\/jats:title><jats:p>Patients who were diagnosed with Beh\u00e7et's disease with parenchymal neurological involvement and underwent infliximab treatment for at least 12\u00a0months were included in the study. Demographic, clinical, and radiological data of the patients were accessed through the electronic database of our hospital.<\/jats:p><\/jats:sec><jats:sec><jats:title>Results<\/jats:title><jats:p>This study comprises 19 patients who were diagnosed with neuro\u2010Beh\u00e7et's disease and used infliximab: 12 male and 7 female patients. The mean age of the patients was 36.5\u00a0\u00b1\u00a011.7\u00a0years, and the diagnostic age was 26.3\u00a0\u00b1\u00a010.8\u00a0years. The duration of treatment with infliximab was 32.3\u00a0months (minimum 11, max 79). In the 19 patients receiving infliximab treatment, 11 (58%) patients achieved remission (complete disappearance of neurological symptoms) and 7 (37%) patients achieved disease stability (no new neurological findings); steroid treatments were discontinued for these 18 patients. In addition, only 5 patients were concomitantly taking immunosuppressive drugs with the infliximab. Infliximab was discontinued after the development of a new parenchymal attack in the 9th month of infliximab treatment.<\/jats:p><\/jats:sec><jats:sec><jats:title>Conclusion<\/jats:title><jats:p>In conclusion, parenchymal neurological involvement in Beh\u00e7et's disease is an important cause of disability, and no sufficient data exists in literature on its treatment. The results of our study suggest that infliximab treatment was effective and safe in neuro\u2010Beh\u00e7et\u2019s disease parenchymal involvement for preventing long\u2010term neurological attacks and discontinuing corticosteroid treatment.<\/jats:p><\/jats:sec>","DOI":"10.1111\/1756-185x.14209","type":"journal-article","created":{"date-parts":[[2021,8,24]],"date-time":"2021-08-24T07:54:28Z","timestamp":1629791668000},"page":"1302-1307","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":18,"title":["Infliximab therapy in parenchymal neuro\u2010Beh\u00e7et\u2019s disease: A single\u2010center experience"],"prefix":"10.1111","volume":"24","author":[{"given":"Demet","family":"Yalcin Kehribar","sequence":"first","affiliation":[{"name":"Department of Rheumatology Medical Faculty Ondokuz May\u0131s University Samsun Turkey"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-1131-2531","authenticated-orcid":false,"given":"Serkan","family":"Gunaydin","sequence":"additional","affiliation":[{"name":"Department of Rheumatology Medical Faculty Ondokuz May\u0131s University Samsun Turkey"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Metin","family":"Ozgen","sequence":"additional","affiliation":[{"name":"Department of Rheumatology Medical Faculty Ondokuz May\u0131s University Samsun Turkey"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"311","published-online":{"date-parts":[[2021,8,24]]},"reference":[{"key":"e_1_2_9_2_1","doi-asserted-by":"publisher","DOI":"10.1007\/s11926-003-0066-9"},{"key":"e_1_2_9_3_1","doi-asserted-by":"publisher","DOI":"10.1097\/BOR.0000000000000458"},{"key":"e_1_2_9_4_1","doi-asserted-by":"publisher","DOI":"10.1007\/s13317\u2010016\u20100074\u20101"},{"key":"e_1_2_9_5_1","doi-asserted-by":"publisher","DOI":"10.1093\/rheumatology\/35.2.139"},{"key":"e_1_2_9_6_1","doi-asserted-by":"publisher","DOI":"10.1093\/rheumatology\/kew486"},{"issue":"5","key":"e_1_2_9_7_1","first-page":"820","article-title":"The prevalence of Beh\u00e7et's syndrome in a rural area in northern Turkey","volume":"15","author":"Yurdakul S","year":"1988","journal-title":"J Rheumatol"},{"key":"e_1_2_9_8_1","doi-asserted-by":"publisher","DOI":"10.1155\/2019\/7371458"},{"key":"e_1_2_9_9_1","doi-asserted-by":"publisher","DOI":"10.1111\/j.1756-185X.2010.01549.x"},{"key":"e_1_2_9_10_1","doi-asserted-by":"publisher","DOI":"10.1097\/00005792-200301000-00006"},{"key":"e_1_2_9_11_1","doi-asserted-by":"publisher","DOI":"10.1016\/j.msard.2019.101512"},{"key":"e_1_2_9_12_1","doi-asserted-by":"publisher","DOI":"10.1007\/s11910-018-0843-5"},{"key":"e_1_2_9_13_1","doi-asserted-by":"publisher","DOI":"10.1007\/s10067\u2010010\u20101414\u20106"},{"issue":"8697","key":"e_1_2_9_14_1","first-page":"1078","article-title":"Criteria for diagnosis of Beh\u00e7et's disease. 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