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Health After eaRly Menopause Due to Oophorectomy

Conditions
BRCA2 Mutation
Menopause Surgical
Cardiovascular Diseases
Bone Mineral Density
Surgical Menopause
BRCA1 Mutation
Cognitive Decline
Quality of Life
Interventions
Diagnostic Test: CAC-score
Registration Number
NCT03835793
Lead Sponsor
The Netherlands Cancer Institute
Brief Summary

Risk-Reducing Salpingo-Oophorectomy (RRSO) at the age of 35 to 45 years is recommended for women with a high genetic risk for ovarian cancer. While this procedure decreases the risk of ovarian cancer by 80-96%, it also results in an immediate menopause. Current research on potential adverse effects of premenopausal risk-reducing salpingo-oophorectomy, such as increased risk of cardiovascular disease, compromised bone health, cognitive dysfunction and reduced quality of life, is limited, mostly due to short follow up.

The investigators will conduct a multicenter cross-sectional study nested in a cohort of BRCA mutation carriers from 8 Dutch centers for hereditary cancer. Eligible participants are women who underwent RRSO before the age of 45. The participants will be frequency-matched on current age with women above the age of 55 without RRSO or with RRSO after the age of 55. Participants will complete an online questionnaire containing various questions about lifestyle, medical history, risk factors for cardiovascular disease, bone health, cognition and quality of life. Participants will be asked to visit one of the participating hospitals for a blood test, a cardiovascular assessment and a DEXA scan for determining bone mineral density. Afterwards participants will be requested to perform the online Amsterdam Cognition Scale.

Detailed Description

Rationale: Women at high genetic risk of ovarian cancer are advised to undergo risk-reducing salpingo-oophorectomy (RRSO) at ages 35-45 years. Currently, in the Netherlands \~500 women/ year opt for RRSO, which minimizes ovarian cancer risk and may decrease breast cancer (BC) risk as well, due to reduced gonadal hormone levels. Besides favorable effects of RRSO on ovarian cancer and, potentially, BC risk, RRSO induces immediate menopause, which may have unfavorable long-term health consequences. Early menopause has been associated with increased risks of cardiovascular disease (CVD), lower bone mineral density (BMD), cognitive impairment, and decreased quality of life. Current evidence regarding these health effects is mainly based on women with a natural early menopause, and it is unknown whether these results hold for women undergoing RRSO at early premenopausal ages.

Objective: The investigators will investigate long-term health effects of premenopausal RRSO on (subclinical) cardiovascular status, BMD, cognition and quality of life.

Study design: the investigators will assess long-term health effects of RRSO in a cross-sectional study, among 500 women who underwent premenopausal RRSO compared to 250 women of the same age without RRSO (or with RRSO after age 55). Eligible women will be invited to participate in a screening program assessing cardiovascular status, bone mineral density, cognitive functioning and quality of life.

Study population: Women are eligible for the premenopausal RRSO group if:

* RRSO before the age of 45 years;

* RRSO was done 10 or more years ago; Women are eligible for the comparison group without premenopausal RRSO if the participant did not undergo RRSO before the age of 55 years, and did not have a natural or therapy induced menopause before age 50.

Primary study outcome: To study long-term effects of premenopausal RRSO on:

* (subclinical) CVD

* BMD

* Cognition

Secondary study outcome: To study long-term effects of premenopausal RRSO on:

* Quality of life

* Urogenital problems

* Cardiovascular risk factors

Furthermore, the investigators will examine the influence of age at RRSO, time since RRSO, hormone replacement therapy (HRT), carrier ship of a BRCA1 or BRCA2 mutation and BC history on the outcome.

The obtained knowledge will assist physicians in counselling women with high ovarian cancer risk and help them to make well-informed decisions.

Recruitment & Eligibility

Status
UNKNOWN
Sex
Female
Target Recruitment
750
Inclusion Criteria
  • RRSO before age 45
  • RRSO after age 55
  • no RRSO
Exclusion Criteria
  • metastatic disease
  • Premature ovarian insufficiency
  • Physical or mental problems interfering with a outpatient visit
  • nonbioabsorbable cardiac stent
  • insufficient understanding of the Dutch language

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
Early-RRSOCAC-score* RRSO before the age of 45 years * RRSO was done 10 or more years ago
Late-/non-RRSO groupCAC-score* Natural menopause ≥ 50 years of age * No RRSO ≤ age of 55 * No treatment-induced menopause ≤ 50 years of age
Primary Outcome Measures
NameTimeMethod
What is the prevalence of atherosclerotic diseases in women with RRSO compared to women with a high genetic risk of ovarian cancer with a natural menopause as assessed by pulse wave velocity in meters/second4 years

Due to the lack of estrogen we expect more atherosclerotic diseases.

What is the prevalence of osteoporosis in women with a premenopausal RRSO compared to women with a high genetic risk of ovarian cancer with a natural menopause as assessed by instant vertebral assessment4 years

Loss of estrogen can result in more activity of osteoclasts and less activity of osteoblasts

What is the prevalence of osteoporosis in women with a premenopausal RRSO compared to women with a high genenetic risk of ovarian cancer with a natural menopause as assessed by beta-CTX in picogram/mililiter4 years

Loss of estrogen can result in more activity of osteoclasts and less activity of osteoblasts

What is the prevalence of cognitive decline in women with RRSO compared to women with a natural menopause as assessed by the Amsterdam Cognition Scan4 years

There are some studies suggesting that an early menopause has an influence on cognition

What is the prevalence of atherosclerotic diseases in women with RRSO compared to women with a high genetic risk of ovarian cancer with a natural menopause as assessed by high-sensitive CRP in miligram/liter4 years

Due to the lack of estrogen we expect more atherosclerotic diseases.

What is the prevalence of atherosclerotic diseases in women with RRSO compared to women with a high genetic risk of ovarian cancer with a natural menopause as assessed by high-sensitive cardial Troponine T in microgram/liter4 years

Due to the lack of estrogen we expect more atherosclerotic diseases.

What is the prevalence of atherosclerotic diseases in women with RRSO compared to women with a high genetic risk of ovarian cancer with a natural menopause as assessed by coronary artery calcium scoring in agatston units4 years

Due to the lack of estrogen we expect more atherosclerotic diseases.

What is the prevalence of osteoporosis in women with a premenopausal RRSO compared to women with a high genetic risk of ovarian cancer with a natural menopause as assessed by dual-energy X-ray absoptiometry in T- and Z-scores4 years

Loss of estrogen can result in more activity of osteoclasts and less activity of osteoblasts, The DXA-scan is corrected for age, with lower values representing a worse outcome

What is the prevalence of osteoporosis in women with a premenopausal RRSO compared to women with a high genenetic risk of ovarian cancer with a natural menopause as assessed by P1NP in miligram/liter4 years

Loss of estrogen can result in more activity of osteoclasts and less activity of osteoblasts

Secondary Outcome Measures
NameTimeMethod
Quality of life after a premenopausal RRSO compared to women from families with a high genetic risk of ovarian cancer with a natural menopause as assessed by validated questionnaires such as the SF-364 years

How do women with a premenopausal RRSO experience their life. The SF-36 questionnaire ranges from 36 to 149, with higher values representing a worse outcome

Quality of life after a premenopausal RRSO compared to women from families with a high genetic risk of ovarian cancer with a natural menopause as assessed by validated questionnaires such as the FACT-ES4 years

How do women with a premenopausal RRSO experience their life. The FACT-ES questionnaire ranges from 0 to 76, with higher values representing a worse outcome

What is the prevalence of urogenital problems in women with a RRSO compared to women with a natural menopause as assessed by validated questionnaires such as the SAQ4 years

Have women with a premenopausal RRSO more urogenital complaints due to longer duration of estrogen deficiency.

The SAQ questionnaire scale has questions with different weights as described in Thirlaway et al. 1996

What is the prevalence of cardiovascular risk factors in women with RRSO compared to women with a high genetic risk of ovarian cancer as assessed by a questionnaire.4 years

Are some risk factors for cardiovascular disease more prevalent in women with a premenopausal RRSO

Quality of life after a premenopausal RRSO compared to women from families with a high genetic risk of ovarian cancer with a natural menopause as assessed by validated questionnaires such as the EORTC-QLQ BR23.4 years

How do women with a premenopausal RRSO experience their life. We measure the body image using the EORTC QLQ BR23, with ranges from 2 to 8, with higher values representing a worse outcome

What is the prevalence of urogenital problems in women with a RRSO compared to women with a natural menopause as assessed by validated questionnaires such as the UDI-64 years

Have women with a premenopausal RRSO more urogenital complaints due to longer duration of estrogen deficiency.

The UDI-6 questionnaire scale has a range from 0 to 18, with higher values representing a worse outcome

What is the prevalence of urogenital problems in women with a RRSO compared to women with a natural menopause as assessed by validated questionnaires such as the IIQ-74 years

Have women with a premenopausal RRSO more urogenital complaints due to longer duration of estrogen deficiency.

The IIQ-7 questionnaire scale has a range from 0 to 24, with higher values representing a worse outcome

Trial Locations

Locations (1)

Netherlands Cancer Institute - Antoni van Leeuwenhoek

🇳🇱

Amsterdam, Netherlands

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