Background
Ovarian and endometrial cancers are the two most commonly diagnosed gynecological cancers, with the highest mortality of all gynecological cancers [
1]. Ovarian cancer is the leading cause of cancer death in gynecological malignancies and the fifth leading cause of all cancers in women in the US [
2]. Endometrial cancer is the most common gynecological malignancy in the US, with a death rate that has increased gradually [
3].
Esposito et al. reported in a meta-analysis that metabolic syndrome is associated with an increased risk of ovarian and endometrial cancers [
4]. Hydroxymethylglutaryl-CoA reductase inhibitors (statins) are cholesterol-lowering drugs that are primarily used for hypercholesterolemia therapy. They also have antitumor effects, which have been reported in experimental research on many cancers [
5]. In recent years, the pharmacological functions of statins were found to be effective in several female reproductive diseases [
6‐
9]. Statins inhibit 3-hydroxy-3-methylglutaryl coenzyme A (HMG CoA) reductase, the key enzyme in the mevalonate pathway for cholesterol synthesis. They can down regulate products of the mevalonate pathway, such as farnesyl diphosphate and geranyl diphosphate, which may contribute to regulating tumor cell growth, motility, and differentiation [
10,
11].
Epidemiological studies of statins and the risk of endometrial or ovarian cancers have shown inconsistent results. A recent population-based study of 161,808 postmenopausal women indicated that statin use can reduce the risk of endometrial cancer but not that of ovarian cancer [
12]. In contrast, another study reported that statin use reduced the risk of ovarian cancer [
13]. Previous studies have reported that statin use was associated with a reduced risk of ovarian or endometrial cancer [
14,
15].
Here, we conducted a meta-analysis to investigate the relationship between statin use and the risk of endocrine-related gynecological cancers.
Discussion
The association between statin use and the risk of endometrial or ovarian cancer remains controversial. Sperling et al. [
15] reported no association between statin use and the risk of endometrial cancer, whereas Desai et al. [
12] reported that statins reduced the risk of endometrial cancer. Some studies have reported a significant association between statin use and the risk of ovarian cancer [
13,
25,
36], but others found no such association [
12,
31]. In 2014, Liu et al. [
41] performed a meta-analysis of the effect of statin use on the risk of gynecological cancers and reported that statin use lowered the risk of ovarian cancer but not that of endometrial cancer. The debate has continued after that publication, and the results of more recent studies have also been inconsistent.
Our meta-analysis included 19 studies enrolling 1,999,362 women. Seven of these studies were published after the last meta-analysis in 2014 and included an additional 1,171,122 subjects. Our pooled analysis indicated that statin use did not reduce the risk of ovarian or endometrial cancer. In addition, we conducted subgroup analyses by study type, percentage of cancer cases, quality of studies, and study location to explore sources of heterogeneity. Two RCTs, six cohort studies and 11 case-control studies were included, and there was no significant association between the use of statins and the risk of ovarian or endometrial cancer based on study type. We used the Jadad scale and NOS criterion to assess the quality of the RCTs and observational studies, respectively. The two RCTs were deemed to be of high quality, with Jadad total scores ≥3, and 14 observational studies had NOS scores ≥7, identifying them as high quality. Subgroup analyses based on the quality of studies indicated that no significant association between statin use and the risk of endometrial cancer was observed in studies of high quality or low quality. The studies we included had different numbers of participants, most included large populations, and the percentage of cancer patients was low and varied. However, we found no significant differences in the association of statin use and the risk of ovarian or endometrial cancer in groups with percentages of cancer cases ≥1% versus groups with < 1%. All of the above subgroup analyses supported our pooled conclusions. In the subgroup analyses based on study location, our results showed a similar tendency, with no reduced risk of ovarian or endometrial cancer in statin users, although a subgroup of statin users in Asia did have a significantly reduced risk of endometrial cancer. This result might be due to regional disparities or racial differences. People in different countries have different dietary habits. Patel et al. reported that metabolic syndrome was less prevalent in Asian populations than it is in US populations [
42]. Therefore, the effects of statin use may vary according to location. However, this meta-analysis subgroup (endometrial cancer patients in Asia) included only one study conducted in Asia, which enrolled fewer subjects than in other studies. Hence, the effects of statin use in endometrial cancer patients require further exploration, and our results require validation from additional RCTs enrolling large populations.
Ovarian and endometrial cancers may be associated with diabetes mellitus. Previous studies reported that patients with diabetes mellitus had an increased risk of ovarian cancer, and patients with ovarian cancer and diabetes had poor survival [
43,
44]. The incidence of endometrial cancer is increasing due to global increases in diabetes and obesity [
45,
46], suggesting that we should target women with diabetes. We planned to conduct subgroup analyses of studies enrolling women with diabetes, but the number of studies was limited. Although the risk of endometrial cancer was significantly reduced in statin users, the results require validation with additional studies enrolling larger populations.
Studies investigating the effects of long-term statin use on ovarian or endometrial cancer have reported inconsistent results. Some studies found no association [
34]. In contrast, the meta-analysis of Liu et al. [
41] reported that long-term statin use significantly reduced the risk of ovarian cancer. Our subgroup analyses of long-term statin use included three more studies and 5,817 additional subjects than the previous meta-analysis [
41] and showed no significant association between long-term statin use and the risk of ovarian or endometrial cancer. As we found no reduction in the risk of ovarian or endometrial cancer in statin users, long-term statin use also had no protective effect. The majority of studies of the effect of long-term statin use indicated no reduced risk of ovarian or endometrial cancer in statin users. Indeed, a recent observational study by Desai et al. [
12] reported that the use of pravastatin was associated with an increased risk of ovarian cancer. This study enrolled a large number of female subjects (161,808) and investigated the relationship between different drug types and cancer risk. Thus, the long-term effect of statins must still be considered unanswered, and more RCTs or high-quality observational studies are needed to verify the effects of long-term statin use on ovarian or endometrial cancer.
Our study has some advantages. The meta-analysis included 19 studies enrolling 1,999,362 female subjects and 19,849 cancer cases. Our inclusion and exclusion criteria were based on PICOS criteria. The Jadad scale was used to assess the quality of the RCTs, and the NOS criterion was used to evaluate the quality of the observational studies; most of the studies were high quality. The 2014 meta-analysis [
41] investigated the association between statin use and the risk of gynecological cancers. In contrast, we investigated the association between statin use and the risk of ovarian and endometrial cancers separately. Our meta-analysis included seven more studies and a larger number of participants than the previous meta-analysis, and our results differed from those of the earlier study. Our subgroup analyses based on study type, percentage of cancer cases, study location, and quality of studies largely supported our conclusions.
There were some limitations in our meta-analysis, which will be resolved in future studies. First, in the selected studies, women were prescribed statins primarily to treat metabolic syndrome, which may independently induce ovarian or endometrial cancer. As a result, it was not possible to pool metabolic status for the observational studies included in this meta-analysis. Moreover, in some studies, patients were prescribed other medications in addition to statins. As other medications may be associated with the risk of cancer, for example, the use of metformin or oral contraceptives may lower the risk of gynecologic cancer [
47,
48], and hormone replacement therapy may influence the risk of gynecologic cancer [
49], there was the possibility that our results had bias, which could be of concern. Hence, to confirm the conclusions of this meta-analysis, further RCTs enrolling larger populations to investigate the association between statin use and the risk of ovarian or endometrial cancer are needed.
Second, the heterogeneity of our study was significant. Our study included 2 RCTs and 17 observational studies; the two RCTs included 12 total cancer cases, whereas the largest studies included approximately 5,000 cancer cases [
15]. Among the included observational studies, the study by Lavie et al. [
36] is a case-control trial in which controls were individually matched to cases according to age, sex, clinic and ethnic group. Therefore, the study excluded many confounding factors, which might lead to a more reliable result. As it has been reported that statin use could reduce the risk of endometrial and ovarian cancers, we cannot ignore the important finding. Although our pooled analysis was negative, the majority of the studies we included were retrospective, which may contain selection, information, and confounding bias. More RCTs or high-quality observational studies are needed to confirm or update our meta-analysis. In addition, we extracted RR data directly or indirectly to represent the relationship between statin use and ovarian or endometrial cancer. However, each of the included studies utilized different study designs according to the different statins or different statin doses. Most studies observed the outcomes of overall statin use (rather than that of a particular drug) and cancer risk. Other studies classified statins as lipophilic or hydrophilic [
13,
37] or separately observed different drugs [
15,
33,
35,
39]. As different statins have different half-lives, different types or doses of statin have been proposed to contribute differently to clinical outcomes. However, the results could not be combined because of such differences in the included studies. Most studies did not record the duration of statin use, and other studies evaluating statin duration were not coincident in the observation time. Thus, we could not combine the results according to the duration of statin use specifically, but only extracted data for long-term statin use (> 5 years). Moreover, the studies we included differed in terms of research methods, follow-up time, and source of the population; any of these factors may have induced study heterogeneity.
Third, the sensitivity analysis indicated that excluding studies one-by-one did not alter the corresponding pooled RRs in the ovarian cancer group, which affirmed the robustness of the result. However, for the studies of endometrial cancer, we found that six studies seemed to affect the heterogeneity. When we excluded any one of these six studies from the overall analysis, statistically significant results were obtained. However, the upper limits of the 95% confidence intervals were approximately 1.00. Thus, as we did not think that excluding so many studies was appropriate, we maintained the original pooled results. In addition, when we conducted analyses of statin use and the risk of ovarian cancer, there was no evidence of publication bias. However, in the overall analyses of endometrial cancer, although there was no significance in Begg’s test, Egger’s test was statistically significant, which indicated a potential publication bias. The most likely explanation is the preferential publication of positive findings.
Fourth, the number of RCTs investigating statin use and the risk of ovarian or endometrial cancer was limited. The search retrieved two RCTs with 12 cancer cases but 17 observational studies with 19,837 cancer cases. Moreover, in these RCTs, statins were used to treat patients with coronary heart disease or hyperlipemia. Cancer was not a primary outcome. Hence, the results from the two RCTs were not powerful enough to conclude the outcome of cancers. Thus, further RCTs investigating statin use and the risk of ovarian or endometrial cancer will be required to confirm these results.
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