Effects of a multinutrient-fortified milk drink combined with exercise on functional performance, muscle strength, body composition, inflammation, and oxidative stress in middle-aged women: a 4-month, double-blind, placebo-controlled, randomized trial

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ABSTRACT

Background

Multinutrient protein-enriched supplements are promoted to augment the effects of exercise on muscle mass and strength, but their effectiveness in middle-aged women, or whether there are any additional benefits to physical function, remains uncertain.

Objectives

We aimed to evaluate whether a multinutrient-fortified milk drink (MFMD) could enhance the effects of exercise on functional muscle power (stair climbing) in middle-aged women. Secondary aims were to evaluate the intervention effects on physical function, muscle strength, lean mass (LM), fat mass (FM), bone mineral content (BMC), muscle cross-sectional area (CSA), muscle density, balance, flexibility, aerobic fitness, inflammation, oxidative stress, bone and cartilage turnover, blood pressure, and blood lipids.

Methods

In this 4-mo, double-blind, placebo-controlled, randomized trial, 244 women (45–65 y) participated in a multimodal resistance-type exercise program 3 d/wk, with random allocation to a twice-daily MFMD containing added protein, vitamin D, calcium, milk fat globule membrane (phospholipids and other bioactives), and other micronutrients (Ex + MFMD, n = 123) or an energy-matched placebo (Ex + placebo, n = 121).

Results

A total of 216 women (89%) completed the study. After 4 mo, both groups experienced similar 3.6%–4.3% improvements in the primary outcomes of fast-pace 5- and 10-step stair ascent power. In contrast, Ex + MFMD experienced greater improvements in 5-step regular-pace stair descent time [net difference (95% CI): −0.09 s (−0.18, 0.00 s), P = 0.045], countermovement jump height [0.5 cm (0.04, 1.0 cm), P = 0.038], total body LM [0.3 kg (0.04, 0.60 kg), P = 0.020], FM [−0.6 kg (−1.0, −0.2 kg), P = 0.004], BMC [0.4% (0.1%, 0.6%), P = 0.020], muscle CSA [thigh: 1.8% (0.6%, 2.9%), P = 0.003; lower leg: 0.9% (0.3%, 1.6%), P = 0.005], balance eyes closed [3.3 s (1.1, 5.4 s), P = 0.005], 2-min step performance [8 steps (3, 12 steps), P = 0.003], and sit-and-reach flexibility [1.4 cm (0.6, 2.2 cm), P = 0.026]. MFMD did not enhance the effects of exercise on any measures of muscle strength, gait speed, dynamic balance, reaction time, or blood lipids, and there was no effect of either intervention on blood pressure, markers of inflammation, or cartilage turnover. Ex + placebo had a greater improvement in the oxidative stress marker protein carbonyls (P < 0.01).

Conclusions

In middle-aged women, daily consumption of an MFMD did not enhance the effects of a multimodal exercise program on the primary outcome of stair climbing ascent power, but did elicit greater improvements in multiple secondary outcomes including various other measures of functional performance, LM, muscle size, FM, balance, aerobic capacity, flexibility, and bone metabolism. This trial was registered at www.anzctr.org.au as ACTRN12617000383369.

Keywords:

resistance training
muscle power
muscle mass
milk protein
vitamin D
calcium
milk fat globule membrane
cytokines
bone turnover

Abbreviations used:

AE
adverse event
ALM
appendicular lean mass
ASA24®
Automated Self-Administered 24-Hour Dietary Assessment Tool
BMC
bone mineral content
CMJ
countermovement jump
CSA
cross-sectional area
CTX-II
C-terminal cross-linked telopeptide type II collagen
eGFR
estimated glomerular filtration rate
Ex + MFMD
multicomponent exercise program with a multinutrient-fortified milk drink
Ex + placebo
multicomponent exercise program with a placebo drink
FM
fat mass
FSST
4-square step test
GLMM
generalized linear mixed model
GP
general practitioner/doctor
hs-CRP
high-sensitivity C-reactive protein
LC/MS/MS
liquid chromatography–tandem mass spectrometry
LM
lean mass
MFGM
milk fat globule membrane
MFMD
multinutrient-fortified milk drink
pQCT
peripheral quantitative computed tomography
PRT
progressive resistance training
PTH
parathyroid hormone
P1NP
plasma procollagen type 1 amino-terminal peptide
RCT
randomized controlled trial
SLB
single-leg standing balance
SSJ
static squat jump
TUG
timed-up-and-go test
VDR
vitamin D receptor
O2 max
maximum oxygen uptake
1-RM
1-repetition maximum
25(OH)D
25-hydroxyvitamin D
β-CTX
plasma carboxy-terminal cross-linking telopeptide of type I collagen.

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Supported by a Primary Growth Partnership grant via the Ministry of Primary Industries in New Zealand with Fonterra Co-operative Group Ltd (to LS, CG, and RMD).

The sponsor was not involved in the conduct of the study; the collection, management, or analysis of the data; or the decision to publish the results.

Supplemental Table 1 is available from the “Supplementary data” link in the online posting of the article and from the same link in the online table of contents at https://academic.oup.com/ajcn/.

Data described in the article, code book, and analytic code will not be made available because approval to freely make available the data was not sought or granted from the Deakin University Human Research Ethics Committee.