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临床试验/NCT02445066
NCT02445066已完成早期 1 期

A Pilot Study to Examine the Effects of Vitamin D Supplementation on Mitochondrial Bioenergetics in Older Adults - An EVIDENCE Sub-Study

Wake Forest University Health Sciences2 个研究点 分布在 1 个国家目标入组 15 人开始时间: 2014年10月最近更新:
适应症

试验速览

阶段
早期 1 期
状态
已完成
入组人数
15
试验地点
2
主要终点
Respirometric profiling

研究概览

简要总结

This pilot study is a 4-month open label trial in 15 older (65-89 yrs) men and women with initial 25(OH)D concentrations of 12-<18 ng/mL to explore the effect of increasing 25(OH)D concentrations to ≥30 ng/mL through vitamin D3 supplementation on changes in mitochondrial bioenergetics. We will assess the bioenergetic profile of blood cells isolated mitochondria, and muscle fibers as well as the expression of mitochondrial proteins and regulators of mitochondria biogenesis before and after supplementation. All participants will be given vitamin D3 (4,000 IU/d) for 4 months.

详细描述

In the past two decades, the role of vitamin D has extended beyond bone health to encompass a wide range of biological activities important to muscle function in older adults. Low 25-hydroxyvitamin D (25[OH]D) concentrations (<30 ng/mL) are associated with lower extremity muscle weakness, impaired physical performance, and slower walking speed,(1-8) known risk factors for disability.(9-15) Low 25(OH)D concentrations in older adults have also been associated with frailty as well as the individual frailty components including muscle weakness, slow walking speed, and exhaustion/fatigue.(16-18) Clinical findings of vitamin D deficiency (25(OH)D <12 ng/mL) include proximal muscle weakness, muscle pain, and gait impairments which are often reversed with vitamin D supplementation.(19;20) However, vitamin D's effects on the mechanisms underlying muscle function are not well understood. Recent evidence supports a role for vitamin D in skeletal muscle mitochondrial metabolism. Using 31P-MRS imaging, an increase in maximal mitochondrial oxidative phosphorylation (OXPHOS) has been reported following vitamin D supplementation.(21) Thus, we hypothesize that muscle weakness and slow walking speed in individuals with low 25(OH)D concentrations may in part be due to diminished OXPHOS activity and lower ATP generation in skeletal muscle mitochondria.

Vitamin D insufficiency is common in older adults, ranging from approximately one-third to three-fourths of community-dwelling adults aged ≥70 years depending on the cut-point used (25(OH)D <20 ng/mL or <30 ng/mL, respectively).(22;23) Similarly, bioenergetic decline is broadly associated with increasing age.(24) Thus, examining the association between vitamin D and mitochondrial bioenergetics can improve our understanding of the underlying mechanisms and range of potential benefits of remediating low 25(OH)D concentrations in older adults.

The objective of the study is to obtain preliminary data on the effect of increasing 25(OH)D concentrations among older adults with vitamin D insufficiency to ≥30 ng/mL through vitamin D3 supplementation on 1) bioenergetic profiles of multiple blood cell populations, skeletal muscle mitochondria, and muscle fibers and 2) skeletal muscle mitochondrial mass and biogenesis.

Hypothesis 1: Bioenergetic capacity as well as respiratory control in muscle mitochondria, muscle fibers, and blood cells will be improved following 4 months of vitamin D3 supplementation.

Hypothesis 2: Expression of key mitochondrial proteins (VDAC/Porin and COX4) and regulators of mitochondria biogenesis (PGC1a, SIRT1, SIRT3, and TFAM) will be higher following 4 months of vitamin D3 supplementation.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Other
盲法
None

入排标准

年龄范围
65 Years 至 89 Years(Older Adult)
性别
All
接受健康志愿者

入选标准

  • SPPB score of 10 or less
  • initial serum 25(OH)D concentration of 12-17.9 ng/mL
  • not dependent on a walker
  • willing to provide informed consent and to adhere to the protocol
  • not involved in another behavioral, exercise, or investigational drug intervention study
  • self-reported physical performance difficulty
  • were screened for the EVIDENCE study within the last 2 months

排除标准

  • serious or uncontrolled chronic disease
  • evidence of impaired cognitive function (MoCA<18)
  • taking prescription vitamin D2 or taking >1000 IU/day of vitamin D3 from all sources; taking an oral corticosteroid; taking hormone replacement therapy
  • inability or contraindications to consume daily vitamin D supplements
  • knee or hip surgery within the last 6 months or planned knee or hip surgery within the next year
  • not willing or eligible to undergo a muscle biopsy (on blood thinners)
  • weight loss of greater than or equal to 5% in the past 3 months
  • BMI > 40kg/m2
  • eye surgery within the past month or planned within the next month
  • if the PI feels the participant is unlikely to follow the protocol

结局指标

主要结局

Respirometric profiling

时间窗: 4 months

Respirometry of isolated mitochondria will be performed in order to examine intrinsic mitochondrial function (type1). Respirometry of permeabilized muscle fibers will be performed to assess type 2 alterations in mitochondrial function. Mitochondrial mass and biogenesis will be determined by western blot analysis. Blood based bioenergetic profiling - PBMC's, monocytes, lymphocytes, and platelets will be separated from whole blood and assessed for basal respiration, maximal respiration, ATP linked respiration, spare respiratory capacity, proton leak, and non-mitochondrial respiration.

次要结局

  • Lower extremity muscle power(4 months)
  • Grip strength(4 months)
  • Physical performance(4 months)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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