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1.
Ann Rheum Dis ; 61(10): 948; author reply 948-9, 2002 Oct.
Article in English | MEDLINE | ID: mdl-12228176
2.
Rheumatology (Oxford) ; 41(7): 819-23, 2002 Jul.
Article in English | MEDLINE | ID: mdl-12096234

ABSTRACT

OBJECTIVE: Increasing the accuracy of the diagnosis of Sjögren's syndrome (SS) by placing emphasis on objective findings such as the presence of anti-Ro and anti-La autoantibodies and abnormal salivary gland tissue (SGT) histology is a current issue. In order to obtain optimal disease sensitivity and specificity of SGT findings, histological and immunohistological SGT examinations were compared. The first describes the extent of the lymphocytic infiltrate as a focus score (LFS), whereas the latter describes the composition of the infiltrate as a percentage of IgA-containing plasma cells (IgA%). METHODS: Both the LFS and IgA% score were assessed in 279 SGT biopsies taken from patients with symptoms suggestive of SS. In case histological conclusions did not match immunohistological conclusions patients were assigned to so-called mismatch groups. Patients in the mismatch groups were further classified using objective, serological parameters [rheumatoid factor (RF), anti-Ro, anti-La, anti-nuclear antibodies, gammaglobulin level]. RESULTS: In 249 samples (89%), LFS and IgA% resulted in the same conclusion. Within this group a total of 63 SGT samples (25%) were characteristic for SS showing LFS >1.0 and IgA% <70. In the mismatch groups after serological classification, both false positive as well as false negative scores were observed less frequently for IgA% as compared with LFS (50 vs 75% and 25 vs 50%, respectively). CONCLUSIONS: Additional immunohistological SGT examination provides greater disease sensitivity and specificity than histological SGT examination alone, thereby increasing accuracy of SS diagnosis.


Subject(s)
Lymphocytes/pathology , Plasma Cells/pathology , Salivary Glands, Minor/pathology , Sjogren's Syndrome/pathology , Adult , Aged , Aged, 80 and over , Female , Humans , Immunoglobulin A/metabolism , Lymphocytes/metabolism , Male , Middle Aged , Plasma Cells/immunology , Reproducibility of Results , Salivary Glands, Minor/immunology , Sensitivity and Specificity , Sjogren's Syndrome/immunology
3.
Ann Rheum Dis ; 60(9): 841-5, 2001 Sep.
Article in English | MEDLINE | ID: mdl-11502610

ABSTRACT

BACKGROUND: Physical disability is part of the end point measures in rheumatoid arthritis clinical trials. The Stanford Health Assessment Questionnaire Disability Index (HAQ DI) is often used for this purpose but lacks international uniformity owing to variations in the translated and adapted questionnaires and variations in its calculation. To study the consequences of these variations the previous Dutch HAQ (HAQ90) was revised, resulting in a new Dutch HAQ (HAQ99). OBJECTIVE: To compare DI scores from the two versions, and to study the consequences of applying different calculation methods for the DI score. METHODS: 78 patients completed both the HAQ99 and the HAQ90. To compare the use of different category score calculation methods a post hoc analysis on prospectively collected data obtained in clinical trials was performed. RESULTS: No statistically significant differences were observed between the DI scores of the HAQ90 and the HAQ99 using the alternative method (that is, without correcting for aid and devices). However, correcting for the use of aid or devices or not did result in statistically significant different DI scores. The systematic shift when using the maximum or mean item score for calculation of the category score resulted in non-comparable absolute DI scores. CONCLUSION: The use of HAQ DI questionnaires with different numbers of items and/or categories does not hinder international comparability, except when these variations interfere with the calculation method of the DI (as in the case of questionnaires without a section correcting for devices). For the sake of international uniformity the HAQ or any validated translation should be used and calculated in a standard way, including correcting for the use of aid and devices, and taking the maximum within each category as the category score.


Subject(s)
Health Status , Surveys and Questionnaires/standards , Aged , Female , Humans , Male , Middle Aged , Prospective Studies , Reproducibility of Results , Statistics, Nonparametric , Translations
4.
Ann Rheum Dis ; 60(5): 511-3, 2001 May.
Article in English | MEDLINE | ID: mdl-11302875

ABSTRACT

Sjögren's syndrome (SS) is a chronic autoimmune disease characterised by specific lesions in exocrine glands, so sublabial minor salivary gland biopsy (SLGB) plays an important part in its diagnosis. The extent and composition of the lymphocytic infiltrate in SLGB specimens can be considered as target organ specific parameters. They are quantified after histological and immunohistological examination by a focus score (describing the extent of the infiltrate) and IgA% score (describing the composition of the infiltrate), respectively. However, little is known about the factors that contribute to the extent and composition of the infiltrate and whether these features are reversible as repeated SLGBs are rarely performed. A patient with SS is described who underwent SLGBs before and after treatment with high dose corticosteroids. After treatment there was not only clinical improvement, but also improvement in the histological and immunohistological parameters. Although these findings need to be confirmed in further studies, this suggests that histopathological changes may be reversible in SS. Furthermore, it shows that the potential effects of corticosteroid use should be taken into account when interpreting SLGB specimens. When clinical changes do parallel histological changes, repeated SLGBs might offer a marker for disease activity in patients with SS.


Subject(s)
Glucocorticoids/therapeutic use , Prednisone/therapeutic use , Salivary Glands, Minor/pathology , Sjogren's Syndrome/drug therapy , Sjogren's Syndrome/pathology , Adult , Cyclophosphamide/therapeutic use , Humans , Immunoglobulin A/analysis , Immunohistochemistry , Immunosuppressive Agents/therapeutic use , Lip , Lymphocytes/pathology , Male
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