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Showing papers by "Risto Sankila published in 2010"


Journal ArticleDOI
TL;DR: Large‐scale, population‐based results about the association between statin utilization and the incidence of cancer in Finland found neither beneficial nor harmful associations between the usage of statins and cancer.
Abstract: The consumption of statins (HMG-CoA reductase inhibitors) has been increasing, and a substantial part of the middle-aged and elderly population use them continuously. Because a large fraction of the population is exposed, even a small excess of risk with respect to cancer should be considered. We carried out a record-linkage study in Finland utilizing nationwide databases of reimbursed statin medication and cancer. The study population included all statin users in Finland who had purchased at least 1 prescription between 1996 and 2005 and who had no cancer diagnosis at the date of first purchase. A control population without statin usage was also included. Data consisted of 472,481 pairs of individuals that cumulated 4.2 million person years with an average of 8.8 years of follow-up. Fifty thousand two hundred ninety-four cancer cases were observed. Simvastatin and atorvastatin were the most used substances. The most frequent cancers were prostate, breast, lung, colon, and rectum cancer. In general, no association between the utilization of statins and cancer could be detected. In conclusion, this study adds large-scale, population-based results about the association between statin utilization and the incidence of cancer. We found neither beneficial nor harmful associations between the usage of statins and cancer.

153 citations


Journal ArticleDOI
TL;DR: No clear evidence of neither beneficial nor harmful association between usage of antidepressant and cancer was found and only few associations between the utilization of AD and cancer could be detected.
Abstract: The consumption of antidepressants, especially selective serotonine reuptake inhibitors (SSRI) has been increasing. Because a large fraction of the population is exposed, even a small excess of risk with respect to cancer should be considered. We carried out a record linkage study in Finland utilizing nationwide databases of reimbursed medication and cancer. The study population included all antidepressant drug (AD) users in Finland who had purchased at least 1 prescription between 1998 and 2005, and who had no cancer diagnosis at the date of first purchase. A control population without AD usage (matched by age and sex) was also included. Data consisted of 418,588 pairs of individuals that cumulated 3.3 million person-years with an average of 4.0 years of follow-up. 19,365 cancer cases were observed. The most frequent cancers were breast, prostate, lung, colon, and brain cancer. In general, only few associations between the utilization of AD and cancer could be detected. Over four years exposure to AD showed a weak association with increased colon and breast cancer incidence, which could have been caused by bias. As conclusion, no clear evidence of neither beneficial nor harmful association between usage of antidepressant and cancer was found.

50 citations


Journal ArticleDOI
TL;DR: This study shows that offspring of cancer patients are not at an increased risk of cancer except when the patient has a cancer‐predisposing syndrome, which is directly relevant to counseling cancer survivors with regard to family planning.
Abstract: Cancer treatments have the potential to cause germline mutations that might increase the risk of cancer in the offspring of former cancer patients. This risk was evaluated in a population-based study of early onset cancer patients in Finland. Using the nationwide registry data, 26,331 children of pediatric and early onset cancer patients (diagnosed under age 35 between 1953 and 2004) were compared to 58,155 children of siblings. Cancer occurrence among the children was determined by linkage with the cancer registry, and the standardized incidence ratios (SIRs) were calculated comparing the observed number of cancers with that expected, based on rates in the general population of Finland. Among the 9,877 children born after their parent's diagnosis, cancer risk was increased (SIR 1.67; 95% CI 1.29-2.12). However, after removing those with hereditary cancer syndromes, this increase disappeared (SIR 1.03; 95% CI 0.74-1.40). The overall risk of cancer among the offspring of siblings (SIR 1.07; 95% CI 0.94-1.21) was the same as among the offspring of the patients with non hereditary cancer. Risk of cancer in offspring, born before their parents cancer diagnosis, was elevated (SIR 1.37, 95% CI 1.20-1.54), but removing hereditary syndromes resulted in a diminished and nonsignificant association (SIR 1.08, 95% CI 0.93-1.25). This study shows that offspring of cancer patients are not at an increased risk of cancer except when the patient has a cancer-predisposing syndrome. These findings are directly relevant to counseling cancer survivors with regard to family planning.

43 citations


Journal ArticleDOI
TL;DR: It is concluded that patients diagnosed with MCC have an increased risk for a second cancer, which may in part result from shared etiological factors between MCC and other tumour types, such as immunosuppression or possibly Merkel cell polyomavirus infection.

37 citations


01 Jan 2010
TL;DR: The consumption of statins (HMG-CoA reductase inhibitors) has been increasing, and a substantial part of the middle-aged and elderly population use them continuously because a large fraction of the population is exposed, even a small excess of risk with respect to cancer should be considered as discussed by the authors.
Abstract: The consumption of statins (HMG-CoA reductase inhibitors) has been increasing, and a substantial part of the middle-aged and elderly population use them continuously Because a large fraction of the population is exposed, even a small excess of risk with respect to cancer should be considered We carried out a record-linkage study in Finland utilizing nationwide databases of reimbursed statin medication and cancer The study population included all statin users in Finland who had purchased at least 1 prescription between 1996 and 2005 and who had no cancer diagnosis at the date of first purchase A control population without statin usage was also included Data consisted of 472,481 pairs of individuals that cumulated 42 million person years with an average of 88 years of follow-up Fifty thousand two hundred ninety-four cancer cases were observed Simvastatin and atorvastatin were the most used substances The most frequent cancers were prostate, breast, lung, colon, and rectum cancer In general, no association between the utilization of statins and cancer could be detected In conclusion, this study adds large-scale, population-based results about the association between statin utilization and the incidence of cancer We found neither beneficial nor harmful associations between the usage of statins and cancer

8 citations