Is There A Connection Between Primary Hypophysitis and Celiac Disease?

Zehra Kara, Tuğçe Eşkazan, Serdar Şahin, Emre Durcan, Cem Sulu, Ahmet Numan Demir, Serhat Uysal, Hande Mefkure Özkaya, Erkan Yılmaz, Ali İbrahim Hatemi, İbrahim Murat Bolayırlı, Pınar Kadıoğlu
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引用次数: 0

Abstract

Aim: To investigate the autoimmune and genetic relationship between primary hypophysitis (PH) and celiac disease (CD).

Methods: The study was retrospective and patients with PH followed in our clinic between 2007 and 2022 were evaluated. Clinical, endocrinologic, pathologic, and radiologic findings and treatment modalities were assessed. Patients diagnosed with CD in the Gastroenterology outpatient clinic in 2020-2022 were included in the study as a control group. Information such as sociodemographic data, year of diagnosis, human leukocyte antigen (HLA) DQ2/8 information, CD-specific antibody levels, pathologic results of duodenal biopsy, treatment received, follow-up status, additional diseases, hormone use, and surgical history was obtained from patient records at PH.In patients diagnosed with PH, a duodenal biopsy was obtained, and the tissue was examined for CD by experienced pathologists. Anti-pituitary antibody (APA) and anti-arginine-vasopressin (AAVP) antibody levels of individuals with PH and CD were measured.

Results: The study included 19 patients with lymphocytic hypophysitis, 30 celiac patients, and 30 healthy controls. When patients diagnosed with lymphocytic hypophysitis were examined by duodenal biopsy, no evidence of CD was found in the pathologic findings. The detection rate of HLA-DQ2/8 was 80% in celiac patients and 42% in PH (p=0.044). (APA and AAVP antibodies associated with PH were tested in two separate groups of patients and in the control group. APA and anti-arginine vasopressin (AAVP) levels in PH, CD and healthy controls, respectively M [IQR]: 542 [178-607];164 [125-243]; 82 [74-107] ng/dL (p=0.001), 174 [52-218]; 60 [47-82]; 59 [48-76] ng/dL (p=0.008) were detected. The presence of an HLA-DQ2/8 haplotype correlates with posterior hypophysitis and panhypophysitis (r=0.598, p=0.04 and r=0.657, p=0.02, respectively).

Conclusion: Although patients with PH were found to have significant levels of HLA-DQ2/8, no CD was found in the tissue. Higher levels of pituitary antibodies were detected in celiac patients compared with healthy controls, but no hypophysitis clinic was observed at follow-up. Although these findings suggest that the two diseases may share a common genetic and autoimmune basis, the development of the disease may be partially explained by exposure to environmental factors.

原发性垂体炎和乳糜泻之间有联系吗?
目的探讨原发性垂体炎(PH)与乳糜泻(CD)之间的自身免疫和遗传关系。方法回顾性分析2007年至2022年在我院随访的PH患者。评估临床、内分泌、病理、放射学表现和治疗方式。2020-2022年在胃肠病学门诊诊断为乳糜泻的患者作为对照组纳入研究。社会人口统计数据、诊断年份、HLA DQ2/8信息、乳糜泻特异性抗体水平、十二指肠活检病理结果、接受的治疗、随访情况、其他疾病、激素使用和手术史等信息均从ph的患者记录中获得。对于诊断为原发性垂体炎的患者,进行十二指肠活检,并由经验丰富的病理学家检查组织是否患有乳糜泻。测定PH和CD患者的抗垂体和抗精氨酸-抗利尿激素抗体水平。结果本研究包括19例淋巴细胞性垂体炎患者、30例乳糜泻患者和30例健康对照。当诊断为淋巴细胞性垂体炎的患者通过十二指肠活检检查时,病理结果未发现乳糜泻的证据。乳糜泻患者HLA-DQ2/8检出率为80%,原发性垂体炎患者检出率为42% (p=0.044)。在两组单独的患者和对照组中检测与原发性垂体炎相关的抗垂体和抗精氨酸加压素(AAVP)抗体。抗垂体(AP)和抗精氨酸加压素(AAVP)水平在PH、CD和健康对照中的应用[j]: 542 [178-607];164 [125-243];82 [74-107] ng/dl (p=0.001), 174 [52-218];60 (47 - 82);59 [48 ~ 76] ng/dl (p=0.008)。HLA-DQ2/8单倍型的存在与后垂体炎和全垂体炎相关(r=0.598, p=0.04和r=0.657, p=0.02)。结论原发性垂体炎患者虽有明显的HLA-DQ2/8水平,但组织中未发现乳糜泻。与健康对照组相比,乳糜泻患者的垂体抗体水平较高,但随访时未观察到垂体炎临床。虽然这些发现表明这两种疾病可能具有共同的遗传和自身免疫基础,但疾病的发展可能部分归因于暴露于环境因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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