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Dietary Protein Quality for Skeletal Muscle Anabolism in Older Adults

2022年10月5日 更新者:University of Birmingham

The Importance of Dietary Protein Quality for Skeletal Muscle Anabolism in Older Adults

Dietary proteins potently augment muscle protein synthesis. Because of poorer anabolic sensitivity with ageing, studies and guidelines recommend higher dietary protein intake for older adults. Although higher doses would benefit skeletal muscle remodelling, large protein consumption is not feasible for many older adults. To circumvent, high-protein quality which possesses a high amino acid profile and digestibility appears to have an emergent role for supporting anabolism. Since currently the best line of defence against age related muscle loss is resistance exercise training and regular protein consumption, emphasising high-quality protein ingestion, such as whey protein, within meals may be feasible and efficacious in supporting musculoskeletal remodelling in older adults, without requirement for large protein doses.

The investigators propose that at low doses, high quality protein will have additive benefit to muscle protein synthesis compared to low-quality protein. Further, combining high-quality protein diets with resistance exercise training will have more profound benefits for muscle protein synthesis and muscle remodelling more so than low-quality protein diets.

調査の概要

詳細な説明

Participants will be randomly assigned to a 10-day dietary intervention consuming primarily animal proteins (high-quality condition) or primarily plant proteins (low-quality condition). In both conditions, participants will undertake supervised single-leg resistance exercise training every other day, amassing five days resistance exercise sessions during the study. The groups will aim to be matched and counterbalanced for gender. Equally for unilateral exercise randomisation for leg dominance will aim to be counterbalanced within both groups.

Preliminary assessments:

5 days preceding the start of the dietary intervention, participants will report to the University of Birmingham, Sport, Exercise and Rehabilitation Science for the following:

  1. Health questionnaire
  2. Written informed consent
  3. Anthropometrics (Height and Weight)
  4. Body fat (bioelectrical impedance)
  5. Start measuring habitual activity (provided with an activity monitor and pedometer)
  6. Start measuring habitual diet (provided with diet diary)

2 days preceding the start of the dietary intervention, participants will report to the University of Birmingham, Sport, Exercise and Rehabilitation Science for the following:

  1. Saliva sample (participant gives own saliva sample in a tube)
  2. 10ml of blood taken for baseline measures (venepuncture by trained phlebotomist)
  3. Loading dose of D2O (stable isotope of water ingested in 8 small 50ml doses taken 1 hour apart throughout the day)
  4. Find 1 repetition maximum (1RM) during unilateral knee extension.

Dietary intervention each day throughout 10-day intervention participants will provide a saliva sample and then consume a top up dose of D2O, continue wearing an activity tracker and keep a diet diary to record eating times of provided meals.

Meals will be individualised to body weight for each individual to achieve a moderate protein intake of which will then consist of primarily higher quality or lower quality proteins.

Day 0 (first day of diet), participants will report to the University of Birmingham, Sport, Exercise and Rehabilitation Science at 0800h after fasting >10 hours the night prior for the following:

  1. Resting metabolic rate (Laying down for 30 minutes to assess gaseous exchange while wearing a mask)
  2. Muscle architecture (using non-invasive ultrasonography)
  3. Whole-body composition assessment (DXA scan)
  4. Bilateral muscle biopsies (small amount of muscle will be taken from the muscle in the thigh (vastus lateralis) by a trained person from the left and right leg, under local anaesthetic)
  5. Maximal muscle strength (isometric dynamometry) and neural activation (interpolated twitch) during maximal muscle contraction on both legs in series.
  6. Serial blood samples will be taken with a single cannulisation and 8 10ml blood draws taken throughout the visit (before and after consuming a breakfast which is either higher or lower in protein quality, according to the randomised condition).
  7. Perceived appetite will be assessed during the visit, before and after breakfast, using visual analogue scales
  8. Urine collection tub will be provided to collect urine over the next 24-hours.

After consuming specified breakfast on this visit, participants will continue to eat meals given to them according to their random allocation of either higher or lower quality protein diets.

Day 1, 3, 5, 7, 9

Participants will report to the University of Birmingham, Sport, Exercise and Rehabilitation Science to undergo single-leg resistance exercise on a knee extension machine. Eight sets will be completed on the machine at each visit at 75% of 1RM (determined during preliminary visits and will be supervised).

On day 9, the participant will be given a urine collection tub to collect urine over the next 24-hours.

Day 10 (Diet finishing during this visit), participants will report to the University of Birmingham, Sport, Exercise and Rehabilitation Science at 0800h after fasting >10 hours the night prior for the following assessments:

  1. Resting metabolic rate (Laying down for 30 minutes to assess gaseous exchange while wearing a mask)
  2. Whole-body composition assessment (DXA scan)
  3. Muscle Architecture (using non-invasive ultrasonography)
  4. Maximal muscle strength (Isometric Dynamometry) and neural activation during maximal muscle contraction (Interpolated twitch)
  5. Bilateral muscle biopsies (small amount of muscle will be taken from the muscle in the thigh (vastus lateralis) from the left and right leg under local anaesthetic
  6. Serial blood samples will be taken with a single cannulisation and 8 10ml blood draws taken throughout the visit (before and after consuming the final meal of the diet which is the breakfast which is either higher or lower in protein quality, according to the randomised condition)
  7. Perceived appetite will be assessed during the visit, before and after breakfast, using visual analogue scales.

研究の種類

介入

入学 (予想される)

40

段階

  • 適用できない

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究連絡先

  • 名前:Leigh Breen, PhD
  • 電話番号:+44 121 414 4109
  • メールl.breen@bham.ac.uk

研究連絡先のバックアップ

研究場所

    • West Midlands
      • Edgbaston、West Midlands、イギリス、B15 2TT
        • 募集
        • University of Birmingham, School of Sport, Exercise and Rehabilitation Sciences
        • コンタクト:
        • コンタクト:
          • Marie Korzepa, MSc

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

50年~70年 (大人、高齢者)

健康ボランティアの受け入れ

いいえ

受講資格のある性別

全て

説明

Inclusion Criteria:

  • Males and Females aged between 50-70 years
  • Accustomed to normal physical activity levels (averaging at least 7000 steps a day)
  • Healthy body mass (i.e., BMI 18-25 kg/m2)
  • General good health indicated by health questionnaire
  • Free from COVID-19 (SARS-CoV-2) symptoms.

Exclusion Criteria:

  • Habitually high consumers of protein (>1.6g/kg/day) assessed by habitual diet diary
  • Food allergies
  • Lidocaine allergy
  • Smoker
  • Bleeding Disorders
  • Chronic/systemic illnesses (i.e., renal failure, rheumatoid arthritis, diabetes, poor lung function, heart disease, cancer, uncontrolled hypertension)
  • Regular consumption of any analgesic or anti-inflammatory drugs. Taking medications mknown to affect muscle metabolis (e.g. beta-blockers, corticosteroids).

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

研究はどのように設計されていますか?

デザインの詳細

  • 主な目的:基礎科学
  • 割り当て:ランダム化
  • 介入モデル:並列代入
  • マスキング:独身

武器と介入

参加者グループ / アーム
介入・治療
実験的:High Quality Protein
Participants will consume four high-quality protein containing meals per day (amounting to 1g/kg/day of protein) over a 10-day period. Each meal will contain 75:25 animal:plant protein with most of the animal protein from supplemental high-quality protein powder.
Supervised single-leg (unilateral) exercise will be undertaken every other day throughout the dietary intervention
他の名前:
  • Single-leg resistance exercise
Participants will consume a protein supplement alongside a provided diet to control protein amount and quality.
実験的:Low Quality Protein
Participants will consume four low-quality protein containing meals per day (amounting to 1g/kg/day of protein) over a 10-day period. Each meal will contain 25:75 animal:plant protein with most of the plant protein from supplemental low-quality protein powder.
Supervised single-leg (unilateral) exercise will be undertaken every other day throughout the dietary intervention
他の名前:
  • Single-leg resistance exercise
Participants will consume a protein supplement alongside a provided diet to control protein amount and quality.

この研究は何を測定していますか?

主要な結果の測定

結果測定
メジャーの説明
時間枠
Muscle protein synthesis using muscle biopsies and deuterated water enrichment.
時間枠:0-10 days
Muscle protein synthesis will be assessed during the high-quality and low-quality intervention and compared between exercised and controlled leg.
0-10 days
Leg Strength using dynamometry
時間枠:0-10 days
Evaluating change in leg strength, of trained leg, pre- and post-intervention with high-quality and low-quality protein condition
0-10 days
Neural activation using interpolated twitch
時間枠:0-10 days
Assessing change in neural activation via non-invasive interpolated twitch technique of between exercised legs pre-and post intervention in both protein quality conditions
0-10 days
Muscle architecture using ultrasound
時間枠:0-10 days
Using non-invasive ultrasound to determine change of muscle structure with training between protein quality conditions.
0-10 days

二次結果の測定

結果測定
メジャーの説明
時間枠
Appetite regulation using questionnaires
時間枠:0-10 days (3 hours postprandial)
Assessing perceived hunger using a validated, 8 question, 100mm visual analogue scales.
0-10 days (3 hours postprandial)
Appetite regulation, blood
時間枠:0-10 days (3 hours postprandial)
Assessing the secretion of hunger and appetite hormones within the blood after meals which contain high-quality versus low-quality protein.
0-10 days (3 hours postprandial)
Metabolic rate, metabolic cart
時間枠:0-10 days
Evaluating alterations in energy expenditure before and after high-quality or low-quality protein containing meal using a metabolic cart.
0-10 days
Nitrogen balance from urine and dietary protein intake
時間枠:0-10 days (24-hour urine collection)
Evaluating change in nitrogen balance between adhering to high-quality or low-quality protein diets over a 10-day period
0-10 days (24-hour urine collection)
Body composition using Duel- energy x-ray absorptiometry (DXA) scan.
時間枠:0-10 days
Change in body composition (muscle mass, fat mass, bone mineral density) will be evaluated using a DXA scanner before and after adhering to single leg resistance exercise paired with either high-quality or low-quality protein diet.
0-10 days
Muscle fibre specific analysis using immunofluorescence microscopy.
時間枠:0-10 days
Evaluate changes in fibre specific differences in the distribution and localisation of key anabolic markers between trained and untrained legs for both protein quality conditions.
0-10 days
Intramuscular signalling using western blotting
時間枠:0-10 days
Evaluate changes in protein content and phosphorylation from the start to the end of the intervention.
0-10 days
Physical activity levels using accelerometery and pedometer
時間枠:-5-10 days
Monitoring of habitual and habitual physical activity to evaluate if intensity and duration of activity is similar between habitual and intervention.
-5-10 days

協力者と研究者

ここでは、この調査に関係する人々や組織を見つけることができます。

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始 (予想される)

2022年11月1日

一次修了 (予想される)

2023年10月1日

研究の完了 (予想される)

2023年12月1日

試験登録日

最初に提出

2022年9月29日

QC基準を満たした最初の提出物

2022年10月5日

最初の投稿 (実際)

2022年10月10日

学習記録の更新

投稿された最後の更新 (実際)

2022年10月10日

QC基準を満たした最後の更新が送信されました

2022年10月5日

最終確認日

2022年9月1日

詳しくは

本研究に関する用語

医薬品およびデバイス情報、研究文書

米国FDA規制医薬品の研究

いいえ

米国FDA規制機器製品の研究

いいえ

この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。

Resistance Exerciseの臨床試験

3
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