Bilateral oophorectomy at the time of hysterectomy for benign disease is commonly practiced to prevent subsequent development of ovarian cancer.1 Data from the Centers for Disease Control and Prevention show that for women having a hysterectomy between ages 40 years and 44 years, 50% have concurrent oophorectomy, and between ages 45 years and 64 years, 78% have oophorectomy.2 In all, approximately 300,000 U.S. women have a prophylactic oophorectomy every year.
Oophorectomy before menopause leads to an abrupt reduction in endogenous estrogen and androgen production.3 Postmenopausal ovaries continue to produce significant amounts of testosterone and androstenedione, which are converted to estrogen peripherally.4,5 Later age of menopause has been associated with a reduced risk of death from coronary heart disease and stroke, and studies show that preserving ovarian function is associated with a lower risk of coronary heart disease.6–9 Among U.S. women, ovarian cancer accounts for 14,700 deaths per year, whereas coronary heart disease accounts for 326,900 deaths, and stroke accounts for approximately 86,900 deaths each year.10
Ovarian conservation, therefore, might benefit overall survival in women not at high risk for ovarian cancer.11 The objective of this study was to report long-term health outcomes and mortality after ovarian conservation or oophorectomy.
MATERIALS AND METHODS
We used the database from the Nurses’ Health Study cohort, which included 122,700 married registered nurses who were aged 30–55 years in 1976 when the initial questionnaires were mailed. Race was self-reported and the cohort was 94% white, 2% African American, 1% Asian, 1% multiracial, and 2% other. The cohort was relatively homogeneous with regard to education, socioeconomic status, and access to health care.12 Additional questionnaires, updating risk factors and newly diagnosed health conditions, have been sent every 2 years, with response rates of approximately 90% for each cycle. In this cohort, a validation study found self-reported oophorectomy at the time of hysterectomy to be very accurate when compared with medical records.13 Nurses’ Health Study participants with a previous hysterectomy entered study follow-up in 1980. Others entered when they reported having a hysterectomy on the 1982 through 2002 questionnaires. All eligible Nurses’ Health Study participants were initially included before application of exclusion criteria.
Through 2002, 50,432 Nurses’ Health Study participants reported having a hysterectomy without a diagnosis of gynecologic cancer. Women were excluded from this study if they had unilateral or partial oophorectomy (n=4,817), unknown ovarian status at the time of hysterectomy (n=2,559), a prior history of an outcome of interest as described below (n=8,525) or an oophorectomy (n=465) before their hysterectomy, or an unknown age at hysterectomy (n=4,643). Women with missing information on past oral contraceptive use were excluded due to the small number in this category (n=43). The remaining 29,380 women were included in the analysis; 16,345 (55.6%) had a hysterectomy with bilateral oophorectomy, and 13,035 (44.4%) had hysterectomy with ovarian conservation. Submission of a completed self-administered questionnaire was deemed to imply informed consent. The institutional review boards at John Wayne Cancer Institute at Saint John’s Health Center in Los Angeles and Brigham and Women’s Hospital in Boston approved this study.
We focused on incident events and death due to the following conditions: coronary heart disease (International Classification of Diseases, 8th Revision [ICD-8]: 410–414), stroke (ICD-8: 430–438), breast cancer (ICD-8: 174), epithelial ovarian cancer (ICD-8: 183), lung cancer (ICD-8:162), colorectal cancer, (ICD-8: 153, 154), hip fracture (ICD-9: 820.3), pulmonary embolus (ICD-8: 450), and death due to all causes. Hip fracture was confirmed by self-report alone; ovarian cancer was confirmed by medical record review, and all other events were confirmed either by medical record or by the participant in writing or by telephone interview.13 If a diagnosis could not be confirmed or rejected, the event was excluded and the follow-up period was censored thereafter. Cause of death was determined using death certificates, autopsy reports, and medical records. Mortality follow-up using the National Death Index and next of kin was more than 98% complete.14
Participant’s age in months and biennial questionnaire cycle were used as stratification variables in the Cox proportional hazards models. For each outcome analysis, we adjusted for related risk factors: age, age at hysterectomy, diabetes, high blood pressure, hypercholesterolemia, family history of myocardial infarction before age 60, tubal ligation, family history of breast cancer, family history of ovarian cancer, body mass index (BMI), smoking status, use of estrogen therapy (ET), duration of oral contraceptive use, alcohol consumption, physical activity and acetylsalicylic acid use (Table 1). Alcohol consumption, physical activity, and use of acetylsalicylic acid were initially queried in 1980. All data were updated at biennial questionnaire cycles. Family history of ovarian cancer (mother or sister) was first asked in 1992 and, once reported, was not updated. For all variables, missing information was separately noted.
Women contributed person-time from the return of the 1980 questionnaire or the questionnaire on which they first reported having a hysterectomy until report of an outcome of interest, oophorectomy subsequent to hysterectomy, death, or end of follow-up on June 1, 2004. In analyses of incident events, women were censored only upon report of the event under analysis, therefore the numbers of person-years varied for each outcome. We calculated incidence rates by dividing the number of incident cases by the total number of person-years for simple hysterectomy or hysterectomy with bilateral oophorectomy. For multivariable analyses, we used Cox proportional hazards models to estimate relative risk (RR) and corresponding 95% confidence intervals (CIs). Age and questionnaire cycle were stratifying variables in the analyses and were controlled for multiple potential confounders, as described in Table 1 and listed in the footnotes of each table.
The study design stratified the cohort into three subcohorts based on age at hysterectomy: younger than 45 years, 45–54 years, and 55 years or older, and we conducted modeling separately for each. In a secondary analysis of oophorectomy status among those who never used estrogen therapy, women were stratified into two age groups (younger than 50 years and 50 years or older) to gain statistical power, and all analyses were repeated. All data transformations and statistical analyses were performed using SAS 9.1. (SAS Institute Inc., Cary, NC) All P values were based on two-tailed tests with significance of 0.05.
Women with ovarian conservation and those with bilateral oophorectomy had similar baseline distributions of risk factors for cardiovascular disease and cancer, but the latter were slightly older and more likely to be current or past users of hormone therapy (Table 1). After adjustment for multiple relevant risk factors, we compared the two groups in relation to the incidence of fatal and nonfatal events during 24 years of follow-up (Table 2—cancer events, Table 3— noncancer events, Table 4—deaths). Oophorectomy was associated with an increased risk of coronary heart disease; this increase was statistically significant for all women (HR 1.17, 95% CI 1.02–1.35) and for women having oophorectomy before age 45 years (HR 1.26, 95% CI 1.04–1.54). Breast cancer was less frequent among all women having oophorectomy (HR 0.75, 95% CI 0.68–0.84), and the risk was lower among women having oophorectomy before the age of 45 years (HR 0.62, 95% CI 0.53–0.74). Oophorectomy was associated with a markedly reduced risk of ovarian cancer (HR 0.04, 95% CI 0.01–0.09), an increased risk of lung cancer (HR 1.26, 95% CI 1.02–1.56), and a reduction in total cancers (HR 0.90, 95% CI 0.84–0.96). Risks of stroke, hip fracture, colorectal cancer, and pulmonary embolism did not differ significantly between groups.
We documented 3,197 deaths from any cause: 350 women (10.9%) died from coronary heart disease, 219 (6.9%) died from stroke, 230 (7.2%) died from breast cancer, 37 (1.2%) died from ovarian cancer, 336 (10.5%) died from lung cancer, 118 (3.7%) died from colorectal cancer, none died due to hip fracture, 12 (0.4%) died from pulmonary embolism, and 1,895 (59.3%) died from other causes.
Among women having a simple hysterectomy, 1,242 died (527 per 100,000 person-years), and among women having a hysterectomy with bilateral oophorectomy, 1,955 died (648 per 100,000 person-years). In multivariable analysis, oophorectomy increased the risk of death from any cause (HR 1.12, 95% CI 1.03–1.21). For every 24 women having bilateral oophorectomy, at least one women will die prematurely from any cause as a result of the oophorectomy. Analysis of cause-specific mortality found an increased risk of death from CHD (HR 1.28, 95% CI 1.00–1.64), lung cancer (HR 1.31, 95% CI 1.02–1.68), and all cancers (HR 1.17, 95% CI 1.04–1.32), a reduced risk of death from ovarian cancer (HR 0.06, 95% CI 0.02–0.21), and no overall difference in deaths from stroke, breast cancer, or colorectal cancer. For every 130 women having bilateral oophorectomy, one extra death from CHD will occur as a result of the oophorectomy. Analysis of death from pulmonary embolism was precluded by the small numbers of deaths.
We performed an analysis of the 10,094 women who had either bilateral oophorectomy or ovarian conservation and had never used estrogen therapy (ET), stratified by age at hysterectomy younger than 50 years and 50 years or older (Table 5). Those who never used ET who had oophorectomy before age 50 years had a higher risk of incident coronary heart disease (HR 1.98, 95% CI 1.18–3.32). Oophorectomy was associated with a significantly increased risk of stroke for all women (HR 1.85, 95% CI 1.09–3.16) and for women aged younger than 50 years at the time of surgery (HR 2.19, 95% CI 1.16–4.14). Oophorectomy was associated with an increased the risk of lung cancer (HR 2.09, 95% 1.01–4.33). The risk of all-cause death was significantly higher among women aged younger than 50 years at the time of surgery (HR 1.40, 95% CI 1.01–1.96). The risks of breast cancer, colorectal cancer, total cancer, hip fracture, and pulmonary embolus were no different among women who had never used ET.
This large prospective study of women having a hysterectomy for benign disease indicates that concurrent bilateral oophorectomy, after adjustment for multiple independent risk factors, is associated with a higher risk of all-cause mortality, primarily from coronary heart disease and lung cancer, when compared with ovarian conservation. Furthermore, prophylactic oophorectomy did not improve survival at any age. During 24 years of follow-up, among 13,305 women who had ovarian conservation, 34 (0.26%) died from ovarian cancer. We did not find increased risks for colorectal cancer, pulmonary embolus, or hip fracture in any analysis. Whereas breast cancer, ovarian cancer, and all cancers were less frequent, the overall risk of death from cancer was greater among women having oophorectomy. The basis for this paradox is unclear and warrants further study. In a secondary analysis of women who never used estrogen therapy, oophorectomy was associated with an increased risk for incident stroke and lung cancer, and oophorectomy before age 50 years was associated with an increased risk of fatal plus nonfatal coronary heart disease, stroke, and deaths from all causes. Total cancer risk was neither increased nor decreased among women with oophorectomy who had never used ET.
Our study has several strengths. This is the largest prospective study, with the longest follow-up, to examine the effect of oophorectomy on health outcomes in women. Although our study is observational, the Nurses’ Health Study cohort is particularly homogenous relative to a study in the general population, with regard to educational and socioeconomic factors that may possibly confound nonrandomized studies. To reduce the possibility of confounding due to the indication for surgery, women with any prior diagnosis of cancer or prior unilateral oophorectomy were excluded from our analysis. To reduce the possibility of confounding due to the family history, our main analysis was adjusted for both family history of breast or ovarian cancer. We also performed a subset analysis that excluded women with a family history of ovarian cancer (approximately 4.5% of study subjects) and found results similar to those presented in our report (data not shown).
Many previous studies were small or did not adjust for known risk factors for cardiovascular disease.6,15,16 Our study included 29,380 women who had hysterectomies, nearly equally divided between bilateral oophorectomy and ovarian conservation. Although baseline characteristics differed somewhat between groups, we used multivariable analysis to correct for multiple known risk factors associated with all the conditions of interest. Follow-up over the 24 years was high for reported incident diagnoses and updated information on risk factors, and identification of deaths is approximately 98% complete.
Several limitations of our study deserve comment. The study was observational, and oophorectomy or ovarian conservation was self-selected. Despite the biologic plausibility of many of our results and despite accounting for multiple risk factors, it is possible that our findings could be related to the underlying indication for which participants chose oophorectomy or due to uncorrected differences between the groups. Most of the women in this study were white and the results may not be applicable to nonwhite women.
Our results for cardiovascular disease are biologically plausible and supported by experimental evidence. Reduction in endogenous estrogen increases serum lipids, reduces carotid artery blood flow, and increases subclinical atherosclerosis as measured by carotid artery intima-media thickness.17–19
Our results are consistent with other studies. A decision analysis found that ovarian conservation improved survival for women aged younger than 65 years at the time of surgery.20 A cohort study of 1,097 women who underwent hysterectomy and bilateral oophorectomy for benign disease who were matched by age to 2,390 women choosing ovarian conservation found mortality to be higher in women who had prophylactic bilateral oophorectomy before the age of 45 years.16
Earlier age of surgical or natural menopause correlates with increased risk of cardiovascular events.15,21,22 Previous reports from the Nurses’ Health Study found that women with oophorectomy between the ages of 40 years and 44 years, compared with women with intact ovaries, had double the risk of myocardial infarction (RR 2.2, 95% CI 1.2–4.2).7 Oophorectomy after age 50 years increased the risk of developing a first myocardial infarction compared with controls (RR 1.4, 95% CI 1.0–2.0).8 When adjusted for age, death from stroke was reduced 6% per year of delayed menopause (RR 0.94, 95%CI 0.89–1.00).6 A meta-analysis of observational studies found that oophorectomy doubled the risk of cardiovascular disease (RR 2.62, 95% CI 2.05–3.35).9 In that cardiovascular disease is the main cause of death among U.S. women, any increased risk would be expected to increase overall morbidity and mortality, as found in our study.
Ovarian cancer is a low-prevalence disease, and simple hysterectomy may reduce the risk of ovarian cancer. Suggested mechanisms include interruption of transport of potential carcinogens through the reproductive tract, alteration in hormone levels, or induction of protective anti-MUC1 antibodies.23–25 Our analysis found a decreased risk of breast cancer among women after oophorectomy. Women with oophorectomy before age 50 years have been shown to have a 50% decreased risk of breast cancer that persisted for 10 years after surgery.26
We found the increased risk of dying of other cancers exceeded the risk of dying from ovarian cancer (low incidence) and breast cancer (high long-term survival rate) among women having an oophorectomy. The association of oophorectomy with lung cancer was unexpected and warrants further study.
Although postmenopausal estrogen therapy may reduce some of the increased risks we found, after publication of the Women’s Health Initiative results, many women discontinued hormone therapy, and 77% fewer women now start hormones at the time of menopause.27 Likewise, continuation rates for medications that can reduce the risk of cardiovascular disease, such as statins, are as low as 18% for women after one year.28
Our findings provide evidence that, for women not at high risk for ovarian cancer, oophorectomy may adversely affect long-term health outcomes and mortality, and at no age was oophorectomy associated with a survival benefit. Preventive surgery should not be performed if it does not clearly benefit the patient. Therefore, prophylactic oophorectomy, with the goal of improving survival by reducing ovarian cancer, seems not to be supported by our study. Given that approximately 300,000 U.S. women per year undergo elective oophorectomy, these findings have important public health implications.
1. ACOG. ACOG Practice Bulletin No. 89. Elective and risk-reducing salpingo-oophorectomy. Obstet Gynecol 2008;111:231–41.
3. Judd H, Judd G, Lucas W, Yen S. Endocrine function of the postmenopausal ovary: concentration of androgens and estrogens in ovarian and peripheral vein blood. J Clin Endocrinol Metab 1974;39:1020–4.
4. Fogle R, Stanczyk F, Zhang X, Paulson R. Ovarian androgen production in postmenopausal women. J Clin Endocrinol Metab 2007;92:3040–3.
5. Judd H, Lucas W, Yen S. Effect of oophorectomy on circulating testosterone and androstenedione levels in patients with endometrial cancer. Am J Obstet Gynecol 1974;118:793–8.
6. Ossewaarde M, Bots M, Verbeek A, Peeters PH, van der Graaf Y, Grobbee DE, et al. Age at menopause, cause-specific mortality and total life expectancy. Epidemiology 2005;16:556–62.
7. Colditz G, Willett W, Stampfer M, Rosner B, Speizer F, Hennekens C. Menopause and the risk of coronary heart disease in women. N Engl J Med 1987;316:1105–10.
8. Falkeborn M, Schairer C, Naessen T, Persson I. Risk of myocardial infarction after oophorectomy and hysterectomy. J Clin Epidemiol 2000;53:832–7.
9. Atsma F, Bartelink M, Grobbee D, van der Schouw Y. Postmenopausal status and early menopause as independent risk factors for cardiovascular disease: a meta-analysis. Menopause 2006;13:265–79.
10. Kung H, Hoyert D, Xu J, Murphy S. Deaths: Final Data for 2005. Natl Vital Stat Rep 2008;56:1–120.
11. Armstrong K, Schwartz J, Randall T, Rubin S, Weber B. Hormone replacement therapy and life expectancy after prophylactic oophorectomy in women with BRCA1/2 mutations: a decision analysis. J Clin Oncol 2004;22:1045–54.
12. Colditz G, Manson J, Hankinson S. The Nurses’ Health Study: 20-year contribution to the understanding of health among women. J Womens Health 1997;6:49–62.
13. Colditz G, Stampfer M, Willett W, Stason W, Rosner B, Hennekens C, et al. Reproducibility and validity of self-reported menopausal status in a prospective cohort study. Am J Epidemiol 1987;126:319–25.
14. Stampfer MJ, Willett WC, Speizer FE, Dysert DC, Lipnick R, Rosner B, et al. Test of the National Death Index. Am J Epidemiol 1984;119:837–9.
15. van der Schouw YT, van der Graaf Y, Steyerberg EW, Eijkemans JC, Banga JD. Age at menopause as a risk factor for cardiovascular mortality. Lancet 1996;347:714–8.
16. Rocca W, Grossardt B, de Andrade M, Malkasian G, Melton LJ 3rd. Survival patterns after oophorectomy in premenopausal women: a population-based cohort study. Lancet Oncol 2006;7:821–8.
17. Cheung L, Pang M, Lam C, Tomlinson B, Chung T, Haines C. Acute effects of a surgical menopause on serum concentrations of lipoprotein(a). Climacteric 1998;1:33–41.
18. Mihmanli V, Mihmanli I, Kantarci F, Aydin T, Yilmaz M, Ogut G. Carotid pulsatility indices in surgical menopause. Arch Gynecol Obstet 2002;266:96–100.
19. Hodis H, Mack W. Atherosclerosis imaging methods: assessing cardiovascular disease and evaluating the role of estrogen in the prevention of atherosclerosis. Am J Cardiol 2002;89:19E–27E.
20. Parker WH, Broder MS, Liu Z, Shoupe D, Farquhar C, Berek JS. Ovarian conservation at the time of hysterectomy for benign disease. Obstet Gynecol 2005;106:219–26.
21. Løkkegaarda E, Jovanovicb Z, Heitmannc B, Keidingb N, Ottesend B, Pedersend A. The association between early menopause and risk of ischaemic heart disease: influence of Hormone Therapy. Maturitas 2006;53:226–33.
22. de Kleijn M, van der Schouw Y, Verbeek A, Peeters P, Banga J, van der Graaf Y. Endogenous estrogen exposure and cardiovascular mortality risk in postmenopausal women. Am J Epidemiol 2002;155:339–45.
23. Hankinson S, Hunter D, Colditz G, Willett W, Stampfer M, Rosner B, et al. Tubal ligation, hysterectomy, and risk of ovarian cancer. A prospective study. JAMA 1993;270:2813–8.
24. Cramer DW, Welch WR, Berkowitz RS, Godleski JJ. Presence of talc in pelvic lymph nodes of a woman with ovarian cancer and long-term genital exposure to cosmetic talc. Obstet Gynecol 2007;110:498–501.
25. Cramer D, Titus-Ernstoff L, McKolanis J, Welch W, Vitonis A, Berkowitz R, et al. Conditions associated with antibodies against the tumor-associated antigen MUC1 and their relationship to risk for ovarian cancer. Cancer Epidemiol Biomarkers Prev 2005;14:1125–31.
26. Schairer C, Persson I, Falkeborn M, Naessen T, Troisi R, Brinton L. Breast cancer risk associated with gynecologic surgery and indications for such surgery. Int J Cancer 1997;70:150–4.
27. Wegienka G, Havstad S, Kelsey J. Menopausal hormone therapy in a health maintenance organization before and after women’s health initiative hormone trials termination. J Womens Health (Larchmt) 2006;15:369–78.
© 2009 by The American College of Obstetricians and Gynecologists. Published by Wolters Kluwer Health, Inc. All rights reserved.
28. Huser MA, Evans TS, Berger V. Medication adherence trends with statins. Adv Ther 2005;22:163–71.