Cancer in biopsy-proven giant cell arteritis.: A population-based study

被引:31
作者
Gonzalez-Gay, Miguel A.
Lopez-Diaz, Maria J.
Martinez-Lado, Luciana
Pena-Sagredo, Jose L.
Lopez-Agreda, Hugo
Miranda-Filloy, Jose A.
Gonzalez-Juanatey, Carlos
Sanchez-Andrade, Arnalia
Martin, Javier
Llorca, Javier
机构
[1] Hosp Xeral Calde, Div Rheumatol, Lugo 27004, Spain
[2] Hosp Xeral Calde, Div Cardiol, Lugo 27004, Spain
[3] Hosp Univ M Valdecilla, Div Rheumatol, Santander, Spain
[4] CSIC, Granada, Spain
[5] Univ Cantabria, Sch Med, Div Prevent Med & Publ Hlth, E-39005 Santander, Spain
关键词
giant cell arteritis; cancer; malignancy; comorbidity; anemia; inflammation; mortality;
D O I
10.1016/j.semarthrit.2007.03.006
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: To investigate the potential association between giant cell arteritis (GCA) and cancer in a series of consecutive patients diagnosed with biopsy-proven GCA over a 25-year period at the single reference hospital for a well-defined population. Methods: The case records of all patients diagnosed with biopsy-proven GCA at the Department of Medicine of the Hospital Xeral-Calde (Lugo, Northwest Spain) between January 1, 1981 and December 31, 2005 were reviewed. Information on cancer and cause of death over the extended follow-up was assessed. In all cases the presence of cancer was histologically confirmed. Results: Cancer was found in 39 (15.3%) of the 255 GCA patients. Although 7 (18%) of the 39 patients had cancer either at the time or within the first 12 months after GCA diagnosis, the standardized mortality ratio (SMR) due to cancer in patients with biopsy-proven GCA showed no increase (overall SMR 1.06 [0.65-1.60]; men, 0.81; women, 1.50). The time interval between GCA diagnosis and cancer diagnosis was 5.2 +/- 3.8 years (median 4.2 years; interquartile range: 3-7 years). When multivariate analysis adjusted by age and sex was performed, only the presence of dysphagia (adjusted hazards ratio (HR) = 3.90; P = 0.04), abnormal temporal artery on physical examination (adjusted HR = 4.61; P = 0.04), and anemia at the time of GCA diagnosis (adjusted HR = 3.39; P = 0.01) were associated with an increased risk of cancer over the extended follow-up. Conclusion: The results from this series do not support an overall increase of mortality due to cancer in GCA. (c) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:156 / 163
页数:8
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