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Optimizing the Beneficial Health Effects of Exercise for Diabetes: Focus on the Liver!

2016년 2월 27일 업데이트: Bram Brouwers

Due to the western lifestyle, correlated with a high calorie intake and low physical activity, obesity is becoming a major health problem. All over the world obesity reaches epidemic proportions. Obesity is closely linked to type 2 diabetes, a multi-factorial disease that increases the presence of multiple health problems. Until now, exercise and dietary intervention seem to be the single most effective interventions to treat obesity and type 2 diabetes mellitus. In obesity and type 2 diabetes, not only fat accumulation in adipose tissue, but also fat accumulation in the peripheral tissues occurs. Fat accumulation in peripheral tissues has been associated with insulin resistance. Exercise seems to have a positive effect on the accumulation of fat in the peripheral tissue and on the insulin sensitivity in type 2 diabetic patients.

In this study we want to investigate if a prolonged exercise training program can lower the intrahepatic lipid content and can improve the metabolism of the liver in type 2 diabetic patients and patients with non-alcoholic fatty liver disease, and to examine if this leads to improvements in metabolic risk markers. To this end, we will include investigation of the effect of exercise on adipose tissue (inflammatory markers and adipocyte size) and skeletal muscle (ex vivo lipid metabolism) to incorporate the effect of exercise on liver, muscle and adipose tissue and to clarify the crosstalk between these tissues in the pathophysiology of type 2 diabetes.

연구 개요

연구 유형

중재적

등록 (실제)

81

단계

  • 해당 없음

연락처 및 위치

이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.

연구 장소

    • Limburg
      • Maastricht, Limburg, 네덜란드, 6200MD
        • Maastricht University

참여기준

연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.

자격 기준

공부할 수 있는 나이

40년 (성인, 고령자)

건강한 자원 봉사자를 받아들입니다

연구 대상 성별

남성

설명

Inclusion Criteria:

  1. All subjects:

    • Male sex
    • Age 40-70 years
    • BMI 27-35 kg/m2
    • Stable dietary habits
    • Sedentary: No participation in any kind of sports for at least 2 years.
  2. For diabetic patients only:

    • Must be on sulphonylurea or metformin therapy for at least 6 months with constant dose for at least 2 months, or on a dietary treatment for at least 6 months
    • Well-controlled diabetes: fasting plasma glucose concentration ≥ 7.0 mmol/l and < 10.0 mmol/l at the time of screening.
  3. For subjects with non-alcoholic fatty liver disease:

    • Liver fat content ≥ 5,56%, based on the formula of Kotronen et al. and confirmed with MRS.
    • Fasting plasma glucose concentration must be < 7.0 mmol/l
  4. For control subjects:

    • Liver fat content < 5,56%, based on the formula of Kotronen et al. and confirmed with MRS.
    • Normoglycemic according to the WHO criteria (OGTT)

Exclusion Criteria:

  1. All subjects:

    • Female sex
    • Unstable body weight (weight gain or loss > 3 kg in the past three months)
    • Participation in an intensive weight-loss program or in vigorous exercise program during the last year before the start of the study.
    • Active cardiovascular disease. (This will be determined by questionnaires and by screening on medication. Furthermore, all subjects will undergo a physical examination by a medical doctor).
    • Chronic renal dysfunction (creatinine > 2 increased (normal values: 64-104 µmol/l))
    • Use of Thiazolidines (glitazone/rosiglitazone/pioglitazone/troglitazone)
    • Systolic blood pressure > 160 mmHg or diastolic blood pressure > 100 mmHg
    • Haemoglobin < 7.5 mmol/l (anaemia)
    • Blood donor
    • Use of medication known to interfere with glucose homeostasis (i.e. corticosteroids), except for diabetic patients.
    • Use of anti-thrombotic medication
    • Claustrophobia and contra-indications for MRI
    • Abuse of alcohol(> 3 units (1unit = 10 gram ethanol) per day)
    • Abuse of drugs
    • Participation in another biomedical study within 1 month before the first screening visit
  2. For diabetics:

    • Severe diabetes which requires application of insulin or patients with diabetes-related complications
  3. For controls:

    • Liver disease or liver dysfunction (ALAT > 2.5 x increased)

공부 계획

이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.

연구는 어떻게 설계됩니까?

디자인 세부사항

  • 주 목적: 치료
  • 할당: 무작위화되지 않음
  • 중재 모델: 단일 그룹 할당
  • 마스킹: 없음(오픈 라벨)

무기와 개입

참가자 그룹 / 팔
개입 / 치료
실험적: Healthy control
This group will exist of healthy obese that are matched for BMI and age with the type 2 diabetes group and non-alcoholic fatty liver disease group.
Subjects will be training for 12 week, 3 times a week. Two times a week they will perform a 30 minutes bicycle training. Once a week they will perform a 30 minutes resistance training.
실험적: Non-alcoholic fatty liver disease
This group will exist of people that suffer from non-alcoholic fatty liver disease. They will be matched for BMI and age according to the Type 2 diabetes group
Subjects will be training for 12 week, 3 times a week. Two times a week they will perform a 30 minutes bicycle training. Once a week they will perform a 30 minutes resistance training.
실험적: Type 2 diabetes patients
This group will exist of patients that suffer from type 2 diabetes
Subjects will be training for 12 week, 3 times a week. Two times a week they will perform a 30 minutes bicycle training. Once a week they will perform a 30 minutes resistance training.

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
측정값 설명
기간
Proton Magnetic resonance spectroscopy to measure the reduction in liver fat content after a training intervention
기간: 16 weeks
16 weeks
Magnetic resonance spectroscopy to measure the ATP and Pi concentrations in the liver
기간: 16 weeks
16 weeks
13C-methionine breath test to measure hepatic mitochondrial function
기간: 16 weeks
Subjects will drink a solution of 200ml H2O with 13C-Methionine. The following 2 hours, every 10 minutes a breath sample will be taken and analysed to measure the concentration of 13C in the exhaled breath.
16 weeks
Euglycemic-hyperinsulinemic clamp for measurement of insulin sensitivity and metabolic flexibility
기간: 16 weeks
After taking fasting blood samples, a primed constant infusion of glucose is initiated. Plasma glucose levels are clamped at ~5 mmol/L by variable co-infusion of 20 % glucose. Every 5 minutes, blood is sampled for immediate determination of plasma glucose concentration. Glucose infusion rate is adjusted to obtain plasma glucose levels of ~5 mmol/L (euglycemia). A bolus of insulin is then infused. Before and during steady state, substrate oxidation is measured using an indirect calorimeter, which determines metabolic flexibility.
16 weeks
Blood sampling to determine the concentration of cardiovascular risk factors in the blood before and after exercise
기간: 16 weeks
16 weeks

2차 결과 측정

결과 측정
측정값 설명
기간
Peripheral arterial tonometry to measure endothelial function, as a marker for cardiovascular risk.
기간: 16 weeks
16 weeks
Echography of the heart to measure diastolic dysfunction
기간: 16 weeks
16 weeks
Fat biopsy to measure adipose tissue inflammatory markers and adipocyte size before and after training intervention
기간: 16 weeks
A small amount of abdominal subcutaneous adipose tissue (~1g) will be collected under local anaesthesia (2% lidocain) using needle biopsy (with the needle connected to a vacuum syringe). Inflammatory markers in the adipose tissue (e.g. IL-6, IL-8, IL-1b, PAI-1, TNFa, CD68, CD163, CD11b, MCP-1, leptin, adiponectin mRNA expression) and adipocyte size will be analysed
16 weeks
Muscle biopsy to measure muscle mitochondrial density, muscle mitochondrial function and muscle lipid metabolism
기간: 16 weeks
. After local anaesthesia (2.0% Xylocain without adrenaline), a 5-mm diameter side-cutting needle will be passed through a 7-mm skin incision, according to the protocol of the Medical Ethical committee of the Academic Hospital and University of Maastricht. The muscle biopsy will be used to measure ex vivo lipid metabolism, muscle mitochondrial density and muscle mitochondrial function.
16 weeks

공동 작업자 및 조사자

여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

스폰서

수사관

  • 연구 책임자: Patrick Schrauwen, PhD, Maastricht University
  • 수석 연구원: Bram MW Brouwers, M.S., Maastricht University

간행물 및 유용한 링크

연구에 대한 정보 입력을 담당하는 사람이 자발적으로 이러한 간행물을 제공합니다. 이것은 연구와 관련된 모든 것에 관한 것일 수 있습니다.

일반 간행물

연구 기록 날짜

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연구 주요 날짜

연구 시작

2011년 3월 1일

기본 완료 (실제)

2015년 11월 1일

연구 완료 (실제)

2015년 11월 1일

연구 등록 날짜

최초 제출

2011년 3월 16일

QC 기준을 충족하는 최초 제출

2011년 3월 16일

처음 게시됨 (추정)

2011년 3월 17일

연구 기록 업데이트

마지막 업데이트 게시됨 (추정)

2016년 3월 1일

QC 기준을 충족하는 마지막 업데이트 제출

2016년 2월 27일

마지막으로 확인됨

2016년 2월 1일

추가 정보

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