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Statins lower ovarian cancer risk in women over 50


Statins lower ovarian cancer risk in women over 50

Statins are widely used to reduce the risk of cardiovascular diseases and lower blood cholesterol, but attention has recently focused on its role in the prevention of cancer.

A new study published in the International Journal of Cancer has found that use of statin by women aged 50 or older was associated with a significantly lower risk of developing any histologic type of ovarian cancer over the next decade compared with non-statin users. The study also found that the effect was independent of the use of any other concomitant medication.

Also Read: Newer contraceptives reduce ovarian cancer risk in women: BMJ

Daniel W. Cramer, Obstetrics and Gynecology Epidemiology Center, Brigham and Women’s Hospital, Boston, MA, and colleagues assessed whether statin use can lower the risk for epithelial ovarian cancer (EOC). For the purpose, they compared 2,040 women with EOC and 2,100 women without the disease.

The New England Case-Control (NEC) study enrolled participants in three time periods: 1992-1998, 1998-2002, and 2003-2008. “The participants were asked if they ever used statins for at least 6 consecutive months … age at first use of statins, type and quantity, and the duration of use,” the researchers noted. The dose consumed by statin users was determined by recording the number of tablets women took over a specific time period and whether or not the statin was lipophilic or hydrophilic.

Also Read: USPSTF : Screening for ovarian cancer not recommended in women without symptoms

Key Findings:

  • The risk of ovarian cancer was 32% lower among statin users compared with those who did not use a statin.
  • No association between statin use and ovarian cancer was seen in women who began use before age 50.
  • The risk of ovarian cancer was 37% lower in statin users between the ages of 50 and 59 compared with non-users, at an OR of 0.63.
  • Among women age 60 and older, the risk of ovarian cancer was 39% lower among statin users versus non-users, at an odds ratio of 0.61 (95% CI 0.44-0.85).
  • The reduction in ovarian cancer risk was also most apparent among women who had taken a statin for 2.o to 4.9 years, but the benefit was apparent for all invasive cancers as well as for both early and late-stage disease.
  • The benefit of taking a statin on ovarian cancer risk was greater for women who used both a statin and either a non-steroidal anti-inflammatory drug or a statin plus aspirin.
  • The reduction in ovarian cancer risk with statin use was apparent only in women who did not have obesity, who had a body mass index of less than 30 kg/m2, and who did not have either type 1 or type 2 diabetes.

“To our knowledge, this is the first population-based case-control study to report a reduced risk for EOC, along with its major histologic subtypes, associated with statin use,” the investigators wrote.

“We think it is noteworthy that the reduction in risk was seen within a decade of [statin] introduction, with relatively short-term use,” the team added.

An association between statin use and ovarian cancer was not apparent in the 1992-1998 data, but the benefit of taking a statin on ovarian cancer risk became apparent in the later dataset between 1998 and 2002 and gained significance in the 2003 to 2008 data set, Cramer and co-authors found.

Cramer told to MedPage Today that he was not surprised by the effect statins had on the risk of ovarian cancer, though he was still impressed with the magnitude of risk reduction seen in this study. He noted that earlier research in patients at very high risk for either oesophagal or colorectal cancer had also shown that statin use significantly reduced the risk of both of these cancers compared with non-statin use.

“We’ve speculated on various ways statins might derive this benefit, and one way is that they would certainly reduce the amount of estrogen formed from precursors of estrogen in the fat,” Cramer suggested. He also pointed out that since cholesterol has a key role in activating inflammation and angiogenesis, reducing cholesterol with statin use may well block both of these pathways. In addition, he said, the 32% reduction in ovarian cancer risk seen with statin use is relatively similar to the effect observed with an oral contraceptive use or tubal ligation.

Thus, for postmenopausal women at high risk for ovarian cancer, Cramer said statin use might be considered as a means for reducing this risk, although the same does not hold true for either premenopausal women or women harboring the BCRA 1 or 2 mutation: “If a woman knows she has either of these mutations, she really needs to be very closely followed by her gynecologist or oncologist,” Cramer cautioned.

“But for postmenopausal women at high risk for ovarian cancer, it does make some sense,” he added.

For further reference follow the link: https://doi.org/10.1002/ijc.31758

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Source: With inputs from International Journal of Cancer

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