It appears you don't have support to open PDFs in this web browser. To view this file, Open with your PDF reader
Abstract
We evaluated whether thyroid function test (TFT) screening is warranted for patients with autoimmune rheumatic diseases (ARD) by comparing the incidence of hypothyroidism requiring treatment (HRT) in ARD patients and healthy controls (HCs). Medical records of 2307 ARD patients and 78,251 HCs for whom thyroid-stimulating hormone (TSH) levels were measured between 2004 and 2018 were retrospectively reviewed. Cumulative incidence of HRT in ARD patients and HCs was compared. HRT development was evaluated with age- and sex-adjusted Kaplan–Meier curve. Risk factors were identified with Cox proportional hazard models. HRT was significantly more common in ARD patients than in HCs (6.3% vs. 1.9%, P < 0.001). After adjusting for age, sex, and baseline TSH level, hazard ratios for HRT were significantly higher in overall ARD patients (hazard ratio [95% confidence interval] 3.99 [3.27–4.87]; P < 0.001), particularly with rheumatoid arthritis and antinuclear antibody-associated diseases in female, and antinuclear antibody-associated diseases, spondyloarthritis, and vasculitis in male patients. Baseline high TSH level, thyroid-related autoantibody positivity, high IgG, and renal impairment were significant risk factors for hypothyroidism development in ARD patients; 20% of high-risk patients developed HRT during follow-up. HRT was significantly more frequent in ARD patients. Careful TFT screening and follow-up could help detecting clinically important hypothyroidism.
You have requested "on-the-fly" machine translation of selected content from our databases. This functionality is provided solely for your convenience and is in no way intended to replace human translation. Show full disclaimer
Neither ProQuest nor its licensors make any representations or warranties with respect to the translations. The translations are automatically generated "AS IS" and "AS AVAILABLE" and are not retained in our systems. PROQUEST AND ITS LICENSORS SPECIFICALLY DISCLAIM ANY AND ALL EXPRESS OR IMPLIED WARRANTIES, INCLUDING WITHOUT LIMITATION, ANY WARRANTIES FOR AVAILABILITY, ACCURACY, TIMELINESS, COMPLETENESS, NON-INFRINGMENT, MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE. Your use of the translations is subject to all use restrictions contained in your Electronic Products License Agreement and by using the translation functionality you agree to forgo any and all claims against ProQuest or its licensors for your use of the translation functionality and any output derived there from. Hide full disclaimer
Details

1 St. Luke’s International Hospital, Immuno-Rheumatology Center, Tokyo, Japan (GRID:grid.430395.8); St. Luke’s International Hospital, Center for Clinical Epidemiology, Tokyo, Japan (GRID:grid.430395.8)
2 St. Luke’s International Hospital, Immuno-Rheumatology Center, Tokyo, Japan (GRID:grid.430395.8)
3 Juntendo University Urayasu Hospital, Department of Internal Medicine and Rheumatology, Chiba, Japan (GRID:grid.482669.7) (ISNI:0000 0004 0569 1541)
4 St. Luke’s International Hospital, Immuno-Rheumatology Center, Tokyo, Japan (GRID:grid.430395.8); NTT East Japan Kanto Hospital, Department of Rheumatology, Tokyo, Japan (GRID:grid.430395.8)
5 St. Luke’s International Hospital, Immuno-Rheumatology Center, Tokyo, Japan (GRID:grid.430395.8); Kyorin University School of Medicine, Department of Nephrology and Rheumatology, Tokyo, Japan (GRID:grid.411205.3) (ISNI:0000 0000 9340 2869)
6 St. Luke’s International Hospital, Department of Endocrinology, Tokyo, Japan (GRID:grid.430395.8)
7 St. Luke’s International Hospital, Center for Clinical Epidemiology, Tokyo, Japan (GRID:grid.430395.8)