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Sökning: onr:"swepub:oai:DiVA.org:uu-420205" > Association of type...

Association of type 2 diabetes mellitus and antidiabetic medication with risk of prostate cancer : a population-based case-control study

Lin, E. (författare)
Kings Coll London, Sch Canc & Pharmaceut Sci, Translat Oncol & Urol Res TOUR, London, England.
Garmo, Hans (författare)
Kings Coll London, Sch Canc & Pharmaceut Sci, Translat Oncol & Urol Res TOUR, London, England.
Van Hemelrijck, Mieke (författare)
Kings Coll London, Sch Canc & Pharmaceut Sci, Translat Oncol & Urol Res TOUR, London, England.
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Adolfsson, Jan (författare)
Karolinska Inst, Dept Clin Sci Intervent & Technol, Stockholm, Sweden.
Stattin, Pär (författare)
Uppsala universitet,Urologkirurgi
Zethelius, Björn (författare)
Uppsala universitet,Geriatrik
Crawley, Danielle (författare)
Kings Coll London, Sch Canc & Pharmaceut Sci, Translat Oncol & Urol Res TOUR, London, England.
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Kings Coll London, Sch Canc & Pharmaceut Sci, Translat Oncol & Urol Res TOUR, London, England Karolinska Inst, Dept Clin Sci Intervent & Technol, Stockholm, Sweden. (creator_code:org_t)
2020-06-15
2020
Engelska.
Ingår i: BMC Cancer. - : BMC. - 1471-2407. ; 20:1
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • BackgroundProstate cancer (PCa) and type 2 diabetes mellitus (T2DM) are prevalent conditions that often occur concomitantly. However, many aspects of the impact of T2DM, particularly the duration of T2DM and antidiabetic medications, on PCa risk are poorly understood.MethodsTo assess the association of duration of T2DM and antidiabetic medication with PCa risk, we designed a matched case-control study, including 31,415 men with PCa and 154,812 PCa-free men in Prostate Cancer data Base Sweden (PCBaSe) 4.1.ResultsOverall, a decreased risk of PCa was observed for men with T2DM (odds ratio (OR): 0.81, 95% confidence interval (CI): 0.78-0.84), as compared to men without T2DM. The decreased risk of PCa was consistently showed across duration of T2DM. With respect to use of antidiabetic drugs, this inverse association with duration was also found for all medications types, as compared to men without T2DM, including insulin, metformin and sulphonylurea (SU) (e.g. 3-<5yr insulin OR:0.69, 95%CI:0.60-0.80; 3-<5yr metformin OR: 0.82, 95%CI: 0.74-0.91; 3-<5yr SU OR: 0.72, 95%CI: 0.62-0.83). When stratifying by PCa risk categories, this decreased risk was most evident for diagnosis of low and intermediate-risk PCa (low-risk OR: 0.65, 95%CI: 0.66-0.70, intermediate-risk OR: 0.80, 95%CI: 0.75-0.85).ConclusionsThe study showed an inverse association between pre-existing T2DM and PCa across different durations of T2DM and all types of T2DM medication received. This inverse association was most evident for low- and intermediate-risk PCa, suggesting that whilst T2DM and its medication may protect some men from developing PCa, the relationship warrants further study.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Cancer och onkologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Cancer and Oncology (hsv//eng)

Nyckelord

Type 2 diabetes mellitus
Antidiabetic medication
Duration
Prostate cancer risk

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