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Nutritional Supplement and Bone Health in Post-Menopausal Women (MBPS)

Primary Purpose

Bone and Bones, Osteoporosis Risk, Osteoporosis, Postmenopausal

Status
Unknown status
Phase
Not Applicable
Locations
Ireland
Study Type
Interventional
Intervention
PLACEBO
MBPM
Sponsored by
University of Limerick
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional basic science trial for Bone and Bones focused on measuring Post-menopausal, Osteoporosis, Bone Turnover Markers, Dairy Products

Eligibility Criteria

50 Years - 70 Years (Adult, Older Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria:

Post-menopausal women aged 50-70y. Assessed by site-specific BMD to be osteopenic. Assessed by clinical screen to be otherwise healthy and free from other illness or current medication likely to influence the study outcome.

Exclusion Criteria:

Intolerance to dairy-based food products

Sites / Locations

  • University of LimerickRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Placebo Comparator

Active Comparator

Arm Label

PLACEBO

Milk-based protein matrix

Arm Description

Intervention: Dietary Supplement: PLACEBO A group of subjects ingesting a liquid beverage (0.3g per kg body mass ; 1.2kcal/kg body mass) at 10:00pm, 3h post-absorptive of a standardised evening meal. Samples for the measurement of biomarkers of change in the rate of bone turnover appearing in the blood to be collected for the immediate 4h, and excreted in urine, 24h post-ingestion

Intervention: Dietary Supplement: MBPM A group of subjects ingesting a liquid beverage (0.3g per kg body mass ; 1.2kcal/kg body mass) at 10:00pm, 3h post-absorptive of a standardised evening meal. Samples for the measurement of biomarkers of change in the rate of bone turnover appearing in the blood to be collected for the immediate 4h, and excreted in urine, 24h post-ingestion

Outcomes

Primary Outcome Measures

Bone turnover
A balance of the difference between the magnitude and time course of the acute change (0-4h) in serum C-terminal telopeptide of type 1 collagen (CTX) in ng/mL, a measure of bone resorption, and procollagen type 1 amino-terminal propeptide (P1NP) in ng/ml, a measure of bone formation and diurnal change in bone resorption measured by 24h urinary excretion of deoxypyridinoline (Dpd), a marker of bone resorption, normalised to creatinine. Units nmolDPD/mmolCr

Secondary Outcome Measures

Change in regulator of bone metabolism - PTH
The magnitude and time course of the acute change (0-4h) in serum parathyroid hormone (PTH) measured in pmol/L
Change in regulator of bone metabolism - RANKL
The magnitude and time course of the acute change (0-4h) in serum receptor activator of the nuclear factor κB ligand (RANKL) measured in ng/dL
Change in regulator of bone metabolism - OPG
The magnitude and time course of the acute change (0-4h) in serum receptor activator of the osteoprotegerin (OPG) measured in pg/mL
Incretin peptide (GIP)
The magnitude and time course of the acute change (0-4h) in enterogastric peptide glucose-dependent insulinotropic peptide (GIP1-42) measured in pg/mL
Incretin peptide (GLP-1)
The magnitude and time course of the acute change (0-4h) in enterogastric glucagon-like peptide-1 (GLP-17-36) measured in pg/mL

Full Information

First Posted
October 12, 2017
Last Updated
November 6, 2017
Sponsor
University of Limerick
Collaborators
Dairygold Cooperative Society Ltd
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1. Study Identification

Unique Protocol Identification Number
NCT03337971
Brief Title
Nutritional Supplement and Bone Health in Post-Menopausal Women
Acronym
MBPS
Official Title
Evaluation of a Milk-Based Nutritional Supplement to Modify Diurnal Rates of Bone Turnover and Effect a Positive Change in Bone Health in Post-Menopausal Women at Risk of Osteoporosis
Study Type
Interventional

2. Study Status

Record Verification Date
November 2017
Overall Recruitment Status
Unknown status
Study Start Date
October 3, 2017 (Actual)
Primary Completion Date
December 28, 2018 (Anticipated)
Study Completion Date
April 4, 2019 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Limerick
Collaborators
Dairygold Cooperative Society Ltd

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The process of bone remodeling exhibits pronounced diurnal pattern that is important for bone health. A balanced rate of bone resorption is required to maintain bone health, a balance that can be disturbed during the lifecycle to effect net rate of formation (as occurs during growth and development to adulthood) or net resorption (as occurs, for example, during the menopause).The research to be undertaken investigates the pluripotent effect of dairy-based products on the regulation of the diurnal process of bone metabolism in post-menopausal women at risk of osteoporosis.
Detailed Description
Study Design: A block randomised, cross-over design of 24h rates of bone turnover in healthy, post-menopausal women with osteopenia receiving either a milk-based protein supplement (MBPS) or isoenergetic placebo control (PLACEBO). Participants: 16 Post-menopausal women with osteopenia as determined by site-specific bone mineral density BMD (DXA) diagnosed and screened by a clinician and for dietary intake of calcium and Vit D by a clinical dietitian. Subject screening (clinical examination) and dietary intake of calcium and Vit D (by food frequency questionnaire) will precede the experimental protocol. Experimental protocol and data collection: Subjects will attend for a 2 day and 2 night (overnight) residence equipped to conduct residential human trials. The subjects' programmed protocol is as follows; Arrive @ 17:00h with overnight bag; Empty bladder and then provide and retain urine samples for the duration of the stay (assisted collection by researchers); Consume a standardised evening meal (pre-prepared by the research dietitian) and then relax reading/watching films etc; At 20:00h a research nurse will insert a cannula into a superficial arm vein and a blood draw (5ml) will be taken and processed for later analysis; Further blood draws (5ml) will be taken at 22:00h, 2300h, 2400h,0100h and 0200h and the cannula withdrawn; At 22:00h consume either placebo control (PLACEBO) (day 1) OR supplement (MBPM)(day 2) - or vice versa - in randomised order. Retire to bedroom; Consume a standardised breakfast and lunch (pre-prepared by the research dietitian) whilst living in and around the University grounds (i.e. in close proximity to ensure 24h urine collection is complete); Repeat from 2 above to end of 2nd day.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Bone and Bones, Osteoporosis Risk, Osteoporosis, Postmenopausal
Keywords
Post-menopausal, Osteoporosis, Bone Turnover Markers, Dairy Products

7. Study Design

Primary Purpose
Basic Science
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Model Description
A block randomised, cross-over design receiving either a milk-based protein supplement (MBPS) or isoenergetic (corn starch) placebo control (PLACEBO).
Masking
Participant
Masking Description
Single blind (participant only)
Allocation
Randomized
Enrollment
16 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
PLACEBO
Arm Type
Placebo Comparator
Arm Description
Intervention: Dietary Supplement: PLACEBO A group of subjects ingesting a liquid beverage (0.3g per kg body mass ; 1.2kcal/kg body mass) at 10:00pm, 3h post-absorptive of a standardised evening meal. Samples for the measurement of biomarkers of change in the rate of bone turnover appearing in the blood to be collected for the immediate 4h, and excreted in urine, 24h post-ingestion
Arm Title
Milk-based protein matrix
Arm Type
Active Comparator
Arm Description
Intervention: Dietary Supplement: MBPM A group of subjects ingesting a liquid beverage (0.3g per kg body mass ; 1.2kcal/kg body mass) at 10:00pm, 3h post-absorptive of a standardised evening meal. Samples for the measurement of biomarkers of change in the rate of bone turnover appearing in the blood to be collected for the immediate 4h, and excreted in urine, 24h post-ingestion
Intervention Type
Dietary Supplement
Intervention Name(s)
PLACEBO
Intervention Description
A food-grade proprietary product containing corn starch in powder form, flavoured and instantised to be dissolved in water. Supplied by Dairygold Ingredients, Mitchelstown, Co Cork, Ireland
Intervention Type
Dietary Supplement
Intervention Name(s)
MBPM
Intervention Description
A food-grade proprietary product containing per 100g; milk protein (46.4%), carbohydrate (40.6%), fat (0.7%), Vitamin D (2ug); calcium (1840mg) in powder form, flavoured and instantised to be dissolved in water. Supplied by Dairygold Ingredients, Mitchelstown, Co Cork, Ireland
Primary Outcome Measure Information:
Title
Bone turnover
Description
A balance of the difference between the magnitude and time course of the acute change (0-4h) in serum C-terminal telopeptide of type 1 collagen (CTX) in ng/mL, a measure of bone resorption, and procollagen type 1 amino-terminal propeptide (P1NP) in ng/ml, a measure of bone formation and diurnal change in bone resorption measured by 24h urinary excretion of deoxypyridinoline (Dpd), a marker of bone resorption, normalised to creatinine. Units nmolDPD/mmolCr
Time Frame
Pre-ingestion and1,2,3 and 4hours post-ingestion (serum) and Pre-ingestion to +24hour post-ingestion (urine)
Secondary Outcome Measure Information:
Title
Change in regulator of bone metabolism - PTH
Description
The magnitude and time course of the acute change (0-4h) in serum parathyroid hormone (PTH) measured in pmol/L
Time Frame
Pre-ingestion,1,2,3 and 4hours post-ingestion
Title
Change in regulator of bone metabolism - RANKL
Description
The magnitude and time course of the acute change (0-4h) in serum receptor activator of the nuclear factor κB ligand (RANKL) measured in ng/dL
Time Frame
Pre-ingestion,1,2,3 and 4hours post-ingestion
Title
Change in regulator of bone metabolism - OPG
Description
The magnitude and time course of the acute change (0-4h) in serum receptor activator of the osteoprotegerin (OPG) measured in pg/mL
Time Frame
Pre-ingestion,1,2,3 and 4hours post-ingestion
Title
Incretin peptide (GIP)
Description
The magnitude and time course of the acute change (0-4h) in enterogastric peptide glucose-dependent insulinotropic peptide (GIP1-42) measured in pg/mL
Time Frame
Pre-ingestion,1,2,3 and 4hours post-ingestion
Title
Incretin peptide (GLP-1)
Description
The magnitude and time course of the acute change (0-4h) in enterogastric glucagon-like peptide-1 (GLP-17-36) measured in pg/mL
Time Frame
Pre-ingestion,1,2,3 and 4hours post-ingestion

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
50 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Post-menopausal women aged 50-70y. Assessed by site-specific BMD to be osteopenic. Assessed by clinical screen to be otherwise healthy and free from other illness or current medication likely to influence the study outcome. Exclusion Criteria: Intolerance to dairy-based food products
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Philip M Jakeman, PhD
Phone
+35361202800
Ext
2800
Email
phil.jakeman@ul.ie
First Name & Middle Initial & Last Name or Official Title & Degree
Mary Clarke-Moloney, BSc
Phone
+35361204230
Ext
4230
Email
Mary.ClarkMoloney@ul.ie
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Philip M Jakeman, PhD
Organizational Affiliation
University of Limerick
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Limerick
City
Limerick
State/Province
Co Limerick
Country
Ireland
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Philip Jakeman, PhD
Phone
+35361202800
Ext
2800
Email
phil.jakeman@ul.ie
First Name & Middle Initial & Last Name & Degree
Catherine Norton, PhD
Phone
+35361204780
Ext
4780
Email
catherine.norton@ul.ie
First Name & Middle Initial & Last Name & Degree
Philip Jakeman, PhD
First Name & Middle Initial & Last Name & Degree
Catherine Norton, PhD

12. IPD Sharing Statement

Plan to Share IPD
No
Links:
URL
http://ul.ie/4i
Description
Center for Inreventions in Inflammation Infection and Immunity

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Nutritional Supplement and Bone Health in Post-Menopausal Women

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