Influence of Early Menopause on Sympathetic Activation and Cardiovascular Function in Older Women



Status:Recruiting
Conditions:Women's Studies
Therapuetic Areas:Reproductive
Healthy:No
Age Range:60 - 70
Updated:10/11/2018
Start Date:August 1, 2018
End Date:August 31, 2020
Contact:Jeungki Yoo, Ph.D.
Email:JeungkiYoo@Texashealth.org
Phone:214-345-4184

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Women who enter menopause early are at a greater risk for developing cardiovascular disease
later in life as compared to women with normal onset of menopause. This increased risk may be
due to a prolonged length of time with decreased hormone levels post-menopause; however, this
health risk remains understudied. The current study plan to study why women with early
menopause are at higher risk for cardiovascular disease by evaluating their sympathetic
nervous system and heart-blood vessel function. In addition, there is lack of promising
treatment plans for cardiovascular disease in post-menopausal women. Therefore, the current
study will also test the impact of dietary nitrate on post-menopausal women to determine if
it might serve as a potential treatment to reduce risk of cardiovascular disease in older
women.

The current study is recruiting two groups of women aged between 60-70 years old; 1) women
who had early natural/non-surgical menopause (age 40-44 yrs) and 2) women who had normal
natural/non-surgical menopause (age 50-54). The investigators are recruiting women who do not
have any cardiovascular disease, hypertension, diabetes, and other major health issue.

The main hypothesis of the project is that early menopause negatively impacts the heart,
blood vessel and nerve system due to the increased length of time with reduced hormone
levels; which could explain the relationship between early menopause and greater risk of
cardiovascular disease in later life. Sympathetic nerve system and cardiovascular functions
will be evaluated in both groups to compare the impact of prolonged hormone deficiency. In
addition, current study will examine the impact of inorganic nitrate supplementation (beet
root juice) to see if there are any favorable changes after 2 weeks of beet root juice
intake. There are 2 main test visits in the current study.

Visit 1. Nerve system test (maximally take about 5 hours): Participants will rest in the
supine position for ≥ 20 mins. Resting heart rate, breathing rate, finger blood pressure will
be monitored. Cardiac output will be assessed using the acetylene gas rebreathing technique
(1 hour). IV will be inserted for blood draw. Nerve signal search will be performed using a
thin needle behind knee to find a signal from a specific nerve. At the same time,
transcranial Doppler probe will be placed on the head to look at brain blood flow using soft
head gear (1-2 hour). After acceptable signals are obtained, baseline data collection will
begin. It will be followed by handgrip exercise and hand immersion to cold water to examine
neural sympathetic response to different stimuli (30 mins). After this, to evaluate nerve
response to different degrees of passive standings, a bed will be tilted to 30° and 60° for 8
mins each. Blood samples will be obtained in the supine resting position and at the end of
60° tilt (45 mins).

Visit 2. Heart and vessel function assessment (Proximately take 2 hours): All measurements
are non-invasive for this visit. Participants will rest in the supine position for ≥ 20 mins.
Resting heart function will be assessed by ultrasound echocardiography (30mins). Vascular
stiffness measurement will be performed using a probe placed on wrist, neck and leg groin
area (30 mins). Vascular endothelial function will be measured using flow-mediated dilation
and followed by smooth muscle responsiveness test will be performed by measuring brachial
artery diameter changes for 10 min following 0.4 mg sublingual nitroglycerin administration
(1 hour).

After Visit 1-2, participant will be asked to drink either dietary nitrate supplementation or
placebo for 2 weeks (randomly assigned). After 2 weeks intervention, participant will come
back for post-intervention tests which are identical to visit 1 and 2.

After completion of the first intervention, participants will have at least 2 weeks of
wash-out period. After 2 weeks participant will be back to the lab and repeat the visit 1 and
2, as well as 2 weeks of dietary nitrate supplementation or placebo. (For those who received
2 weeks of nitrate supplementation for the first intervention, it will be a placebo for this
intervention. For those who received placebo for the first intervention, it will be a nitrate
supplementation for this intervention). After intervention participants will repeat the visit
1 and 2 again.

Inclusion Criteria:

- Healthy normotensive postmenopausal women

- Current age between 60 and 70 years

- Who have experienced "natural" or non-surgical menopause

Exclusion Criteria:

- Any evidence of cardiopulmonary disease

- History of hormone replacement therapy in the last 5 years

- Chronic kidney disease

- Diabetes mellitus

- Hypertension

- Current abuse of alcohol or drugs and use of tobacco products

- Surgical procedure induced menopause
We found this trial at
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Dallas, Texas 75231
Principal Investigator: Jeungki Yoo, Ph.D
Phone: 214-345-4607
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