Clinical significance of quantitative immunohistology in labial salivary glands for diagnosing Sjogren's syndrome

被引:7
作者
van Woerkom, JM
Kruize, AA
Barendregt, PJ
Kater, L
Hené, R
Bootsma, H
Custers, RJH
Jacobs, JWG
Bijlsma, JWJ
机构
[1] Univ Med Ctr Utrecht, Dept Rheumatol & Clin Immunol, NL-3508 GA Utrecht, Netherlands
[2] Erasmus Univ, Med Ctr, Dept Rheumatol, Rotterdam, Netherlands
[3] Univ Groningen, Univ Med Ctr Groningen, Dept Rheumatol, Groningen, Netherlands
关键词
primary Sjogren's syndrome; sicca syndrome; quantitative immunohistology;
D O I
10.1093/rheumatology/kei191
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives. Because patients with primary Sjogren's syndrome (pSS) are at risk of developing other autoimmune phenomena and malignant lymphoma, it is important to distinguish pSS from non-Sjogren's (nSS) sicca syndrome. However, this distinction might be difficult because of the lack of a gold standard for pSS. We studied the clinical significance of quantitative immunohistology (QIH) in labial salivary glands for diagnosing pSS. Methods. In a model mimicking the making of a clinical diagnosis, five experts diagnosed 396 patients as nSS, 'indefinite', pSS or secondary SS (sSS) using 25 clinical parameters. Patients were diagnosed twice, namely without (yielding gold-standard diagnoses) and with knowledge of QIH. The numbers of changes in diagnosis from 'indefinite' to 'definite' (nSS, pSS or sSS) or vice versa were compared. Patient groups with vs without a changed diagnosis in the four gold-standard diagnosis groups were compared regarding objective autoimmune parameters. Results. Sensitivity, specificity, positive and negative predictive value for abnormal QIH in pSS vs nSS were 93, 86, 76 and 96%, respectively. Changes in diagnosis from 'indefinite' to 'definite' (31%) were found more often (P = 0.00) than changes from 'definite' to 'indefinite' (10%). Knowledge of QIH distinguished patient groups within the gold-standard nSS, indefinite and pSS patient group with regard to autoimmune parameters. Conclusion. In view of the consequences of distinguishing pSS from nSS, these results point to an additional diagnostic role for QIH in clinical practice.
引用
收藏
页码:470 / 477
页数:8
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