Gut Microbiota in Chronic Noncommunicable Diseases
The Development of Preventive Methods for Chronic Noncommunicable Diseases Based on Modulation of Gut Microbiota Composition and Function
調査の概要
研究の種類
入学 (実際)
連絡先と場所
研究場所
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Moscow、ロシア連邦、101990
- National Medical Research Center for Therapy and Preventive Medicine of the Ministry of Healthcare of the Russian Federation
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Moscow、ロシア連邦、119121
- Centre for Strategic Planning and Management of Biomedical Health Risks of the Federal Medical Biological Agency
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参加基準
適格基準
就学可能な年齢
健康ボランティアの受け入れ
受講資格のある性別
サンプリング方法
調査対象母集団
説明
Criteria for groups with arterial hypertension, chronic obstructive pulmonary disease (COPD), asthma, type 2 diabetes mellitus and nonalcoholic fatty liver disease (NAFLD) (both prospective and retrospective)
Inclusion criteria:
All mentioned groups:
- Men and women aged ≥ 18 and <80
- Signed informed consent form
Group of arterial hypertention (inclusion criteria):
- No current treatment of hypertension
- Systolic blood pressure <180 mm Hg and diastolic blood pressure <110 mm Hg
- No clinical signs of other cardiovascular diseases
Group of COPD and asthma (inclusion criteria)
- Medical records, confirming COPD or asthma
- Regular stable treatment of COPD, asthma or any chronic disease for ≥ 4 weeks before the enrollment. If inhaled corticosteroids are being used, regular treatment is required for ≥12 weeks.
- Absence of acute exacerbations of COPD, asthma or any concomitant diseases 4 weeks before the enrollment
- No use of genetically engineered biological drugs
- For patients with COPD after inhalation of salbutamol (400 mcg) the ratio FEV1/FVC is less than 0,70
Group of type 2 diabetes mellitus (inclusion criteria)
- Confirmed type 2 diabetes mellitus
- Stable glucose lowering treatment for ≥ 1 month
- No systemic corticosteroid treatment 4 weeks before the enrollment
Group of NAFLD (inclusion criteria)
- Ultrasound criteria of non-alcoholic fatty liver disease or
- Confirmed non-alcoholic fatty liver disease using FibroMax test
Control group inclusion criteria
- Men and women aged ≥ 18 and <80 years
- Signed informed consent form
Control group for arterial hypertension (inclusion criteria):
1. No history of cardiovascular diseases, COPD or asthma
Control group for COPD and asthma (inclusion criteria):
1. No history of diabetes mellitus, NAFLD, COPD and asthma
Exclusion criteria for all groups
- Age < 18 years and ≥80 years
- Denial of further participation
- Obesity with BMI≥40 kg/m2
- History of organ transplantion
- Psychiatric disorder, limiting participation in the study
- Acute infections
- Exacerbation of chronic infection 2 weeks before the enrollment
- Cancer with no radical treatment
- Pregnancy and lactation
- Alcohol and drug addition
- Chronic kidney disease with GFR <30 ml/min/1.73m2
- Systemic autoimmune diseases
- Inflammatory bowel disease
- Antimicrobial and probiotic treatment 3 months before the enrollment
Additional exclusion criteria adjusted for each group
Group of arterial hypertension (exclusion criteria):
- Ischemic heart disease (angina pectoris, myocardial infarction), cerebrovascular disease (stroke, transient ischemic attack), occlusive peripheral arterial disease, revascularization of any vascular bed.
- Cardiomyopathies
- Symptomatic arterial hypertension
- Diabetes mellitus
- Signs of previous myocardial infarction on ECG
- Arrhythmias (parohysmal arrhythmias, atrial fibrillation, sinoatrial block, atrioventricular block grade II-III)
- Signs of current myocardial ischemia on ECG
- Decompensated heart failure
Group of COPD and asthma (exclusion criteria):
Exacerbation of COPD or asthma 3 months before the enrollment which required antibiotic treatment or systemic corticosteroids.
Group of type 2 diabetes mellitus (exclusion criteria):
- Type 1 diabetes mellitus and other specific types of diabetes
- Severe microangiopathy: proliferative and terminal stage of diabetic retinopathy, chronic kidney disease (GFR < 30 ml/min/1,73 m2) for patients with type 2 diabetes
- The history of moderate, severe and very severe COPD
- The history of moderate or severe asthma
- Vegetarians or vegans
Group of non-alcoholic fatty liver disease (exclusion criteria):
- Chronic liver diseases except NAFLD
- The history of moderate, severe and very severe COPD
- The history of moderate or severe asthma
- Vegetarians or vegans
- Diabetes mellitus
Criteria for groups of heart failure and obstructive atherosclerosis (retrospective)
Inclusion criteria for HF-pEF group:
- Men and women aged ≥ 18 and <80 years
- Signs and symptoms of heart failure
- Left ventricular diastolic dysfunction
- Left ventricular ejection fraction ≥50%
- NT-pro BNP >125 pg/ml
- Signed study informed consent form
Inclusion criteria for HF-rEF group:
- Men and women aged ≥ 35 and <80 years
- Signs and symptoms of heart failure
- Left ventricular ejection fraction <50%
- Signed study informed consent form
Inclusion criteria for obstructive atherosclerosis group:
- Men and women aged ≥ 35 and <80 years
Symptoms and signs of obstructive atherosclerosis of any vascular bed:
- Ischemic heart disease or
- Revascularization of coronary, renal, brachiocephalic or lower extremity arteries or
- carotid endarterectomy or
- chronic lower extremity ischemia or
- history of myocardial infarction, stroke, transient ischemic attack or
- renovascular AH
- atherosclerotic aorta aneurysm
- Signed study informed consent form
Inclusion criteria for control group for HF-pEF, HF-rEF and obstructive atherosclerosis
- Men and women aged ≥ 18 and <80 years.
- No signs or symptoms of chronic heart failure
- No signs of left ventricular diastolic dysfunction
- No history, signs or symptoms of obstructive atherosclerosis of any vascular bed
- Signed study informed consent form
Exclusion criteria for groups with HF-pEF, HF-rEF and obstructive atherosclerosis:
- Age <18 and ≥80 years.
- Refuse to sign study informed consent form
- Body mass index ≥35 kg/m2
- Chronic kidney disease with GFR <30 ml/min/1,73 m2
- Current smoking
- Moderate or severe COPD
- Moderate or severe asthma
- Acute infections or exacerbation of chronic infections 2 weeks prior to study enrollment
- History of allergic reactions to gadolinium contrast
- Hypertrophic cardiomyopathy, dilated cardiomyopathy, restrictive cardiomyopathy: primary, amyloidosis, glycogen storage diseases, hemochromatosis, sarcoidosis, drug induced cardiomyopathy, radiation heart disease, constrictive pericarditis).
- Connective tissue disease
- Cancer with no radical treatment
- Pregnancy or lactation
- Inflammatory bowel disease
- Use of antimicrobial agents, probiotics or systemic corticosteroids 3 months before the enrollment
研究計画
研究はどのように設計されていますか?
デザインの詳細
コホートと介入
グループ/コホート |
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対照群
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Arterial hypertension
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Atherosclerosis occlusive disease
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Heart failure with preserved ejection fraction
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Heart failure with reduced ejection fraction
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Diabetes mellitus, type 2
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Chronic obstructive pulmonary disease and asthma
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Nonalcoholic fatty liver disease
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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 |
時間枠 |
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Significant (p<0,05) correlation (r>0,5) between abundance of Faecalibacterium genus and concentration of lipopolysaccharide
時間枠:on enrollment
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on enrollment
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協力者と研究者
研究記録日
主要日程の研究
研究開始 (実際)
一次修了 (実際)
研究の完了 (実際)
試験登録日
最初に提出
QC基準を満たした最初の提出物
最初の投稿 (実際)
学習記録の更新
投稿された最後の更新 (実際)
QC基準を満たした最後の更新が送信されました
最終確認日
詳しくは
本研究に関する用語
追加の関連 MeSH 用語
その他の研究ID番号
- 3162021
個々の参加者データ (IPD) の計画
個々の参加者データ (IPD) を共有する予定はありますか?
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
米国FDA規制機器製品の研究
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