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SAT0133 (2018)
Prevalence of type 2 diabetes and evaluation of patient characteristics among patients with and without ra from community rheumatologyclinics
E. Alemao1, L. Ferri1, D. Paul1, A. Marshall1, L. McDonald2, A. Rao3, V. R. Anupindi4, G. Craig5, K. Knapp5
1Bristol-Myers Squibb, Princeton, UnitedStates
2Bristol-Myers Squibb, Uxbridge, United Kingdom
3MuSigma, Bangalore, India
4Mu Sigma, Princeton
5DiscusAnalytics LLC, Spokane, United States

 

Background: RA and type 2 diabetes (T2D) have common core pathophysiologic pathways, such as insulin resistance and increased glycated end products related to endothelial dysfunction, which may portendcardiovascular disease.1 Currently there is limited real-world evidence of T2D prevalence among patients (pts) with RA.

Objectives: To estimate the prevalence of T2D and insulin resistance among pts with RA vs control (osteoarthritis [OA] pts). To evaluate characteristics among RA pts with/without T2D.

Methods: A retrospective study was conducted ona subset of the JointMan database (an electronic medical record of >6000 ptsfrom >10 providers. At each visit, diagnosis, medications, test results,co-morbidities and demographic data were collected. Pts aged ≥18 years with ≥2 diagnoses of RA or satisfying ACR criteria from 1 Jan 2009 to 30 Nov 2017 were included with a control group (pts with ≥2 OA diagnoses in the same period). Pts were considered to have T2D if they had a diagnosis code, diabetic medications prescription, HbA1c ≥6.5%, random glucose test ≥200 mg/dL or prior report ofT2D. Between-group prevalence was compared using a chi-squared test and characteristics of pts with/without T2D were compared using Fisher's exact, chi-squared and Mann-Whitney tests.

Results: Data were analysed from 4181, 1157 and 1626 pts in RA-only, OA-only and dual (RA plus OA) cohorts, respectively. The RA-only cohort was younger and had a lower proportion of white pts compared with other cohorts (Table). T2D prevalence was significantly higher in the dual cohort (24.3%, n=395) vs RA-only (16.2%, n=676; p<0.001) and OA-only cohorts(10.5%, n=121; p<0.001). T2D prevalence was significantly higher in the RA-only vs OA-only cohorts (p<0.001). Sicca and Sjögren's syndromes were more prevalent co-morbidities in pts with RA only with vs without T2D (16.3 vs13.0%; p=0.023) and a similar trend was observed for thyroid disorder (6.4 vs 3.7%; p=0.001).

Table 1 Pt Characteristics by Cohort
RA only (n=4181) OA only (n=1157) Dual (RA plus OA) (n=1626)
With T2D (n=676) No T2D (n=3505) With T2D (n=121) No T2D (n=1036) With T2D (n=395) No T2D (n=1231)
Age (years), mean (SD) 59.6 (13.5) 59.6 (14.8) 68.6 (9.8) 65.4 (11.4) 64.7 (10.5) 64.5 (11.1)
Female, n (%) 504 (74.6) 2643 (75.4) 83 (68.8) 761 (73.5) 294 (74.4) 943 (76.6)
Race, n (%)
American Indian or Alaska Native 29 (4.3) 71 (2.0) 6 (5.0) 9 (0.9) 12 (3.0) 27 (2.2)
White 521 (77.1) 2579 (73.6) 105 (86.8) 921 (88.9) 363 (91.9) 1127 (91.6)
Co-morbidities, n (%)
Sicca/Sjögren's syndromes 110 (16.3) 456 (13.0) 20 (16.5) 117 (11.3) 92 (23.3) 356 (28.9)
Thyroid disorders 43 (6.4) 128 (3.7) 3 (2.5) 65 (6.3) 27 (6.8) 68 (5.5)
Charlson Comorbidity Index, mean (SD) 1.02 (0.15) 1.01 (0.18) 1.05 (0.34) 1.01 (0.12) 1.01 (0.14) 1 (0.09)

Conclusions: A higher prevalence of T2D was observed in pts with RA compared with controls. In addition, co-morbidities of Sjögren's syndrome and thyroid disorder were higher in T2D pts with RA but not for dual RA plus OA.

Reference:

  1. de Groot L, et al. Arthritis Res Ther 2011;13:R205.

Disclosure of Interest: E. AlemaoShareholder of: Bristol-Myers Squibb, Employee of: Bristol-Myers Squibb, L.Ferri Employee of: Bristol-Myers Squibb, D. Paul Employee of: Bristol-Myers Squibb, A. Marshall Share holder of: Bristol-Myers Squibb, Employee of:Bristol-Myers Squibb, L. McDonald Employee of: Bristol-Myers Squibb, A. Rao Consultant for: Bristol-Myers Squibb, V. Anupindi Consultant for: Mu Sigma, G.Craig Share holder of: Discus Analytics, Grant/research support from: Bristol-Myers Squibb, Consultant for: Premera Blue Cross/Blue Shield of Washington and Alaska, Celgene, Bristol-Myers Squibb, Genentech, Novartis, Employee of: Arthritis Northwest, Paid instructor for: Washington State University Elson Floyd School of Medicine; University of Washington, Speakers bureau: Bristol-Myers Squibb, UCB, Genentech, Celgene, Novartis, Abbvie,Sanofi/Regeneron, Eli Lily, K. Knapp Shareholder of: Discus Analytics, LLC, Employee of: Discus Analytics, LLC

DOI: 10.1136/annrheumdis-2018-eular.2582



Citation: Ann Rheum Dis, volume 77, supplement Suppl, year 2018, page A928
Session: Rheumatoid arthritis - comorbidity and clinical aspects