Use of drugs for hyperlipidaemia and diabetes and risk of primary and secondary brain tumours: nested case-control studies using the UK Clinical Practice Research Datalink (CPRD)

被引:0
作者
Robinson, Jamie W. [1 ]
Martin, Richard [1 ,2 ,3 ]
Ozawa, Mio [4 ]
Elwenspoek, Martha Maria Christine [2 ,5 ]
Redaniel, Maria Theresa [2 ,5 ]
Kurian, Kathreena M. [1 ,6 ]
Ben-Shlomo, Yoav [2 ,5 ]
机构
[1] Univ Bristol, MRC Integrat Epidemiol Unit, Bristol, England
[2] Univ Bristol Med Sch, Dept Populat Hlth Sci, Bristol, England
[3] Univ Hosp Bristol, Natl Inst Hlth Res NIHR, Bristol Biomed Res Ctr, Bristol, England
[4] UCL Great Ormond St Inst Child Hlth, Populat Policy & Practice Res & Teaching Dept, London, England
[5] Univeristy Bristol, Natl Inst Hlth Res NIHR, Collaborat Leadership Appl Hlth Res Care CLAHRC We, Bristol, England
[6] Univ Bristol, Brain Tumour Res Ctr, Bristol, England
关键词
Epidemiology; Head & neck tumours; CLINICAL PHARMACOLOGY; EPIDEMIOLOGIC STUDIES; Neurological oncology;
D O I
暂无
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives Previous studies have suggested that fibrates and glitazones may have a role in brain tumour prevention. We examined if there is support for these observations using primary care records from the UK Clinical Practice Research Datalink (CPRD). Design We conducted two nested case-control studies using primary and secondary brain tumours identified within CPRD between 2000 and 2016. We selected cases and controls among the population of individuals who had been treated with any anti-diabetic or anti-hyperlipidaemic medication to reduce confounding by indication. Setting Adults older than 18 years registered with a general practitioner in the UK contributing data to CPRD. Results We identified 7496 individuals with any brain tumour (4471 primary; 3025 secondary) in total. After restricting cases and controls to those prescribed any anti-diabetic or anti-hyperlipidaemic medication, there were 1950 cases and 7791 controls in the fibrate and 480 cases with 1920 controls in the glitazone analyses. Longer use of glitazones compared with all other anti-diabetic medications was associated with a reduced risk of primary (adjusted OR (aOR) 0.89 per year, 95% CI 0.80 to 0.98), secondary (aOR 0.87 per year, 95% CI 0.77 to 0.99) or combined brain tumours (aOR 0.88 per year, 95% CI 0.81 to 0.95). There was little evidence that fibrate exposure was associated with risk of either primary or secondary brain tumours. Conclusions Longer exposure to glitazones was associated with reduced primary and secondary brain tumour risk. Further basic science and population-based research should explore this finding in greater detail, in terms of replication and mechanistic studies.
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页数:9
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