Autonomic Regulation of Blood Pressure in Premature and Early Menopausal Women

Sponsor
University of Minnesota (Other)
Overall Status
Recruiting
CT.gov ID
NCT04439370
Collaborator
(none)
160
1
39
4.1

Study Details

Study Description

Brief Summary

This is a cross-sectional study in which the investigators will determine the impact of premature/early menopause on MSNA, BP and baroreflex sensitivity in younger (≤49 yr old) and older (≥50 yr old) women. Specifically, aim one will determine mechanisms driving autonomic dysregulation of BP in premature and early menopausal women and aim two will determine mechanisms driving autonomic dysregulation of BP in older menopausal women. The study design outlined below will permit testing of aim one and aim two.

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: Microneurography to measure muscle sympathetic nerve activity (MSNA)
  • Diagnostic Test: Baroreflex sensitivity testing
  • Diagnostic Test: Sympathoexcitatory Maneuvers
  • Diagnostic Test: Blood tests

Detailed Description

Aim One: Determine mechanisms driving autonomic dysregulation of blood pressure (BP) in premature and early menopausal women. Because sympathetic activity and baroreflex function are important contributors for autonomic support of BP regulation, these two mechanisms will be assessed in premature and early menopausal women who are ≤49 yr old. To specifically identify the influence of menopause, these women will be compared to age-matched premenopausal women. The primary hypothesis is that there is greater resting sympathetic activity and blunted baroreflex function in premature and early menopausal women compared with age-matched premenopausal women. The secondary hypothesis is that BP and sympathetic reactivity will be greater in premature and early menopausal compared with age-matched premenopausal women when the sympathetic nervous system is challenged with a stressor.

Aim Two: Determine mechanisms driving autonomic dysregulation of BP in older menopausal women. Because older age contributes to risk of CVD, it is imperative to assess the long-term effects of premature and early menopause in older (≥50 yr) women. To determine the impact of the premature loss of sex hormones on cardiovascular physiology, women whom have lived without functioning ovaries for >10 yr will be compared to age-matched women who entered menopause at a typical age. The primary hypothesis is that resting sympathetic activity is greater and baroreflex function is attenuated in women who experience premature or early menopause compared with typically-aged menopausal women. The secondary hypothesis is that BP and sympathetic reactivity will be greater in premature and early compared with typically-aged menopausal women when the sympathetic nervous system is challenged with a stressor.

Study Design

Study Type:
Observational
Anticipated Enrollment :
160 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Autonomic Regulation of Blood Pressure in Premature and Early Menopausal Women
Actual Study Start Date :
Oct 1, 2019
Anticipated Primary Completion Date :
Jan 1, 2023
Anticipated Study Completion Date :
Jan 1, 2023

Arms and Interventions

Arm Intervention/Treatment
Aim 1: Postmenopausal Women

Participants in this group are postmenopausal women.

Diagnostic Test: Microneurography to measure muscle sympathetic nerve activity (MSNA)
Microneurography is a direct measurement of electrical activity of peripheral sympathetic nerves

Diagnostic Test: Baroreflex sensitivity testing
Two arms of the baroreflex that will be tested in this study are sympathetic and cardiovagal. Static baroreflex is tested during baseline resting conditions and dynamic baroreflex is tested during Valsalva maneuvers.

Diagnostic Test: Sympathoexcitatory Maneuvers
Cold Pressor Test (CPT) and Upper extremity fatiguing contraction with post exercise circulatory occlusion (PECO) will be performed

Diagnostic Test: Blood tests
Serum FSH, estrogen, progesterone, and testosterone will be measured

Aim 1: Premenopausal Women

Participants in this group are premenopausal women.

Diagnostic Test: Microneurography to measure muscle sympathetic nerve activity (MSNA)
Microneurography is a direct measurement of electrical activity of peripheral sympathetic nerves

Diagnostic Test: Baroreflex sensitivity testing
Two arms of the baroreflex that will be tested in this study are sympathetic and cardiovagal. Static baroreflex is tested during baseline resting conditions and dynamic baroreflex is tested during Valsalva maneuvers.

Diagnostic Test: Sympathoexcitatory Maneuvers
Cold Pressor Test (CPT) and Upper extremity fatiguing contraction with post exercise circulatory occlusion (PECO) will be performed

Diagnostic Test: Blood tests
Serum FSH, estrogen, progesterone, and testosterone will be measured

Aim 2: Premature/Early Menopause

Participants in this group women who experienced premature or early menopause.

Diagnostic Test: Microneurography to measure muscle sympathetic nerve activity (MSNA)
Microneurography is a direct measurement of electrical activity of peripheral sympathetic nerves

Diagnostic Test: Baroreflex sensitivity testing
Two arms of the baroreflex that will be tested in this study are sympathetic and cardiovagal. Static baroreflex is tested during baseline resting conditions and dynamic baroreflex is tested during Valsalva maneuvers.

Diagnostic Test: Sympathoexcitatory Maneuvers
Cold Pressor Test (CPT) and Upper extremity fatiguing contraction with post exercise circulatory occlusion (PECO) will be performed

Diagnostic Test: Blood tests
Serum FSH, estrogen, progesterone, and testosterone will be measured

Aim 2: Typical-Age Menopause

Participants in this group are women who experienced menopause at a typical age.

Diagnostic Test: Microneurography to measure muscle sympathetic nerve activity (MSNA)
Microneurography is a direct measurement of electrical activity of peripheral sympathetic nerves

Diagnostic Test: Baroreflex sensitivity testing
Two arms of the baroreflex that will be tested in this study are sympathetic and cardiovagal. Static baroreflex is tested during baseline resting conditions and dynamic baroreflex is tested during Valsalva maneuvers.

Diagnostic Test: Sympathoexcitatory Maneuvers
Cold Pressor Test (CPT) and Upper extremity fatiguing contraction with post exercise circulatory occlusion (PECO) will be performed

Diagnostic Test: Blood tests
Serum FSH, estrogen, progesterone, and testosterone will be measured

Outcome Measures

Primary Outcome Measures

  1. Muscle Sympathetic Nerve Activity (MSNA) (bursts per minute) [3 hours]

    Muscle sympathetic nerve activity (MSNA) is a measurement of sympathetic activity. This is measured by two small needles are inserted behind or on the side of the knee, one needle is an acupuncture needle and one needle is a small recording microelectrode (same size as the acupuncture needle). Outcome will be reported in units of bursts per minute.

  2. Muscle Sympathetic Nerve Activity (MSNA) (bursts/100 heart beats) [3 hours]

    Muscle sympathetic nerve activity (MSNA) is a measurement of sympathetic activity. This is measured by two small needles are inserted behind or on the side of the knee, one needle is an acupuncture needle and one needle is a small recording microelectrode (same size as the acupuncture needle). Outcome will be reported in units of bursts per 100 heart beats.

  3. Cardiac baroreflex sensitivity [3 hours]

    Baroreflex sensitivity will be derived from electrocardiogram measurements and blood pressure measurements during the baseline rest period and by performing a modified valsalva maneuver which involves exhaling against 30-40 mmHg of pressure over 15 seconds after a normal inhalation. Outcome will be reported in units as ms/mmHg.

  4. Sympathetic baroreflex sensitivity [3 hours]

    Baroreflex sensitivity will be derived from electrocardiogram measurements and blood pressure measurements during the baseline rest period and by performing a modified valsalva maneuver which involves exhaling against 30-40 mmHg of pressure over 15 seconds after a normal inhalation. Outcome will be reported in units of MSNA bursts/mmHg.

  5. Systolic Blood Pressure (mmHg) [3 hours]

    Blood pressure is measured using a non-invasive blood pressure cuff secured to the middle or ring finger and reported in units of mmHg.

  6. Diastolic Blood Pressure (mmHg) [3 hours]

    Blood pressure is measured using a non-invasive blood pressure cuff secured to the middle or ring finger and reported in units of mmHg.

  7. Mean Arterial Blood Pressure (mmHg) [3 hours]

    Blood pressure is measured using a non-invasive blood pressure cuff secured to the middle or ring finger and reported in units of mmHg.

  8. Heart Rate (beats/min) [3 hours]

    Heart rate will be measured with a three-lead electrocardiogram (ECG) and reported in units of beats/min.

Secondary Outcome Measures

  1. Respiratory Rate (breaths/min) [3 hours]

    Respiratory rate will be measured with a belt placed around the stomach and reported in units of breaths-per-minute.

  2. Heart Rate Variability (frequency) [3 hours]

    Heart rate variability will be measured using electrocardiogram and reported in units of Hertz.

  3. Heart Rate Variability (time) [3 hours]

    Heart rate variability will be measured using electrocardiogram and reported in units of milliseconds.

  4. Borg Rating of Perceived Exertion [3 hours]

    Participants will be asked to rate their perceived exertion using the Borg Rating of Perceived Exertion scale. Scores range from 6-20 with higher scores indicating greater exertion.

  5. Numerical Pain Scale Rating [3 hours]

    Participants will be asked to rate pain on a scale from 0 to 10. Higher scores indicate greater pain.

  6. Blood Levels: Estrogens-E1 [75 minutes]

    Serum concentration of estrogen-E1 will be reported in units of ng/ml.

  7. Blood Levels: Estrogen-E2 [75 minutes]

    Serum concentration of estrogen-E2 will be reported in units of ng/ml.

  8. Blood Levels: Progesterone [75 minutes]

    Serum concentration of progesterone will be reported in units of ng/ml.

  9. Blood Levels: Testosterone [75 minutes]

    Serum concentration of testosterone will be reported in units of ng/ml.

  10. Blood Levels: Follicle-Stimulating Hormone (FSH) [75 minutes]

    Serum concentration of FSH will be reported in units of IU/L.

  11. Upper extremity fatiguing contraction with post exercise circulatory occlusion (PECO) [3 hours]

    This test involves holding a hand grip device at 30% of the participant's maximum hand grip strength until they fatigue. At the end of this test a blood pressure cuff is inflated for two minutes. The outcome measurements are the total change in systolic, diastolic and mean blood pressure from rest as well as how much blood pressure changes every 15 seconds. The measurement units are the change in blood pressure in mmHg.

  12. Cold Pressor Test [3 hours]

    The cold pressor test is done by placing the participant's hand in a bucket of ice-cold water for 2 minutes. The outcome measurements are the total change in systolic, diastolic and mean blood pressure from rest as well as how much blood pressure changes every 15 seconds. The measurement units are the change in blood pressure in mmHg.

Eligibility Criteria

Criteria

Ages Eligible for Study:
35 Years to 70 Years
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Aged 35-49 or 50-70 years of age who experienced premature (<40) or early (≤45) menopause

  • Premenopausal 35-49 years of age

  • Typical-age menopause (i.e., after 45 years of age), who are between 50-70 years old

  • Menopause will be confirmed by subject report of amenorrhea for 12 months and serum FSH of >30 mIU/mL

Exclusion Criteria:
  • Current nicotine/tobacco use within the past six months

  • Are diabetic or asthmatic

  • Have diagnosed significant carotid stenosis

  • Have a history of significant autonomic dysfunction, heart disease, respiratory disease or a severe neurologic condition such as stroke or traumatic brain injury.

  • Have existing metabolic or endocrine abnormities

  • Take any heart/blood pressure medications that are determined to interfere with study outcomes

  • IF the participant is premenopausal AND currently taking OC or other exogenous steroids that are determined to interfere with study outcomes

  • Females who classify as having early or premature menopause AND are not willing to discontinue OC or MHT in order to complete the study

  • Are pregnant or breastfeeding

Contacts and Locations

Locations

Site City State Country Postal Code
1 University of Minnesota Minneapolis Minnesota United States 55455

Sponsors and Collaborators

  • University of Minnesota

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
University of Minnesota
ClinicalTrials.gov Identifier:
NCT04439370
Other Study ID Numbers:
  • STUDY00007978
First Posted:
Jun 19, 2020
Last Update Posted:
Sep 27, 2021
Last Verified:
Sep 1, 2021
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Sep 27, 2021