PLoS One. 2014;9(10):e109433.
Electronic medical record cancer incidence over six years comparing new users of glargine with new users of NPH insulin.
제1저자 임수 · 교신저자 Meigs JB
소속 (5)
- General Medicine Division, Department of Medicine, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts, United States of America; Department of Internal Medicine, Seoul National University College of Medicine and Seoul National University Bundang Hospital, Seongnam, Korea.
- General Medicine Division, Department of Medicine, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts, United States of America; Center for Human Genetic Research, Department of Medicine, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts, United States of America.
- General Medicine Division, Department of Medicine, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts, United States of America.
- Division of Endocrinology, University of North Carolina School of Medicine, Chapel Hill, North Carolina, United States of America.
- Department of Epidemiology, Gillings School of Global Public Health, University of North Carolina, Chapel Hill, North Carolina, United States of America.
Abstract
BACKGROUND Recent studies suggested that insulin glargine use could be associated with increased risk of cancer. We compared the incidence of cancer in new users of glargine versus new users of NPH in a longitudinal clinical cohort with diabetes for up to 6 years.
METHODS AND FINDINGS From all patients who had been regularly followed at Massachusetts General Hospital from 1/01/2005 to 12/31/2010, 3,680 patients who had a medication record for glargine or NPH usage were obtained from the electronic medical record (EMR). From those we selected 539 new glargine users (age: 60.1±13.6 years, BMI: 32.7±7.5 kg/m2) and 343 new NPH users (61.5±14.1 years, 32.7±8.3 kg/m2) who had no prevalent cancer during 19 months prior to glargine or NPH initiation. All incident cancer cases were ascertained from the EMR requiring at least 2 ICD-9 codes within a 2 month period. Insulin exposure time and cumulative dose were validated. The statistical analysis compared the rates of cancer in new glargine vs. new NPH users while on treatment, adjusted for the propensity to receive one or the other insulin. There were 26 and 28 new cancer cases in new glargine and new NPH users for 1559 and 1126 person-years follow-up, respectively. There were no differences in the propensity-adjusted clinical characteristics between groups. The adjusted hazard ratio for the cancer incidence comparing glargine vs. NPH use was 0.65 (95% CI: 0.36-1.19).
CONCLUSIONS Insulin glargine is not associated with development of cancers when compared with NPH in this longitudinal and carefully retrieved EMR data.
Figures
그림 출처: PubMed Central 공개 논문 (PMC4203726)
Conflict of interest statement
Competing Interests:The funding for this project was provided by Sanofi (Paris, France) through a subcontract with the University of North Carolina at Chapel Hill. This does not alter the authors’ adherence to PLOS ONE policies on sharing data and materials. There are no patents, products in development or marketed products to declare.
그 밖의 정보
- 출판 형태
- Comparative Study, Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't
- 저널
- PloS one · eISSN 1932-6203
- 전자 출판
- 2014-10-20
- MeSH
- Diabetes Mellitus / drug therapy · Disease-Free Survival · Electronic Health Records* · Female · Humans · Incidence · Insulin Glargine · Insulin, Isophane / adverse effects / therapeutic use · Insulin, Long-Acting / adverse effects / therapeutic use · Male · Middle Aged · Neoplasms / chemically induced · Time Factors
- Substances
- Insulin, Long-Acting · Insulin Glargine · Insulin, Isophane
- 연구비
- NIDDK NIH HHS K24 DK080140 · NIA NIH HHS R01 AG023178
- 참고문헌
- 22편
