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Gut Microbiota in Chronic Noncommunicable Diseases

18. april 2022 oppdatert av: Anastasia Kaburova, National Medical Research Center for Therapy and Preventive Medicine

The Development of Preventive Methods for Chronic Noncommunicable Diseases Based on Modulation of Gut Microbiota Composition and Function

It is an observational study in patients with chronic noncommunicable diseases (i.e. cardiovascular diseases, diabetes mellitus, non-alcoholic fatty liver disease, chronic obstructive pulmonary disease and asthma ) and control group with no signs of these conditions. The study has a prospective part planned for 2021 and a retrospective part which includes the patients enrolled between 2018-2020. The aim of the study is to investigate gut microbiota composition, its metabolites, levels of inflammatory and other markers of the disease in prospective groups (arterial hypertension, type 2 diabetes mellitus, chronic obstructive pulmonary disease, asthma, non-alcoholic fatty liver disease and control patients) as well as in retrospective groups (chronic heart failure with preserved and reduced ejection fraction, obstructive atherosclerosis of any vascular bed, arterial hypertension, type 2 diabetes mellitus, chronic obstructive pulmonary disease, asthma, non-alcoholic fatty liver disease, and control patients). Also we are planning to investigate the association between gut microbiota composition and its metabolites, levels of inflammatory and other markers of the disease in retrospective and prospective groups.

Studieoversikt

Studietype

Observasjonsmessig

Registrering (Faktiske)

1084

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiesteder

      • Moscow, Den russiske føderasjonen, 101990
        • National Medical Research Center for Therapy and Preventive Medicine of the Ministry of Healthcare of the Russian Federation
      • Moscow, Den russiske føderasjonen, 119121
        • Centre for Strategic Planning and Management of Biomedical Health Risks of the Federal Medical Biological Agency

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

18 år til 79 år (Voksen, Eldre voksen)

Tar imot friske frivillige

Nei

Kjønn som er kvalifisert for studier

Alle

Prøvetakingsmetode

Ikke-sannsynlighetsprøve

Studiepopulasjon

Patients with chronic noncommunicable diseases including cardiovascular diseases, type 2 diabetes mellitus, nonalcoholic fatty liver disease, chronic obstructive pulmonary disease, asthma and control group

Beskrivelse

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):

  1. No current treatment of hypertension
  2. Systolic blood pressure <180 mm Hg and diastolic blood pressure <110 mm Hg
  3. No clinical signs of other cardiovascular diseases

Group of COPD and asthma (inclusion criteria)

  1. Medical records, confirming COPD or asthma
  2. 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.
  3. Absence of acute exacerbations of COPD, asthma or any concomitant diseases 4 weeks before the enrollment
  4. No use of genetically engineered biological drugs
  5. 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)

  1. Confirmed type 2 diabetes mellitus
  2. Stable glucose lowering treatment for ≥ 1 month
  3. No systemic corticosteroid treatment 4 weeks before the enrollment

Group of NAFLD (inclusion criteria)

  1. Ultrasound criteria of non-alcoholic fatty liver disease or
  2. Confirmed non-alcoholic fatty liver disease using FibroMax test

Control group inclusion criteria

  1. Men and women aged ≥ 18 and <80 years
  2. 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

  1. Age < 18 years and ≥80 years
  2. Denial of further participation
  3. Obesity with BMI≥40 kg/m2
  4. History of organ transplantion
  5. Psychiatric disorder, limiting participation in the study
  6. Acute infections
  7. Exacerbation of chronic infection 2 weeks before the enrollment
  8. Cancer with no radical treatment
  9. Pregnancy and lactation
  10. Alcohol and drug addition
  11. Chronic kidney disease with GFR <30 ml/min/1.73m2
  12. Systemic autoimmune diseases
  13. Inflammatory bowel disease
  14. Antimicrobial and probiotic treatment 3 months before the enrollment

Additional exclusion criteria adjusted for each group

Group of arterial hypertension (exclusion criteria):

  1. Ischemic heart disease (angina pectoris, myocardial infarction), cerebrovascular disease (stroke, transient ischemic attack), occlusive peripheral arterial disease, revascularization of any vascular bed.
  2. Cardiomyopathies
  3. Symptomatic arterial hypertension
  4. Diabetes mellitus
  5. Signs of previous myocardial infarction on ECG
  6. Arrhythmias (parohysmal arrhythmias, atrial fibrillation, sinoatrial block, atrioventricular block grade II-III)
  7. Signs of current myocardial ischemia on ECG
  8. Decompensated heart failure

Group of COPD and asthma (exclusion criteria):

  1. 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):

  2. Type 1 diabetes mellitus and other specific types of diabetes
  3. 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
  4. The history of moderate, severe and very severe COPD
  5. The history of moderate or severe asthma
  6. Vegetarians or vegans

Group of non-alcoholic fatty liver disease (exclusion criteria):

  1. Chronic liver diseases except NAFLD
  2. The history of moderate, severe and very severe COPD
  3. The history of moderate or severe asthma
  4. Vegetarians or vegans
  5. Diabetes mellitus

Criteria for groups of heart failure and obstructive atherosclerosis (retrospective)

Inclusion criteria for HF-pEF group:

  1. Men and women aged ≥ 18 and <80 years
  2. Signs and symptoms of heart failure
  3. Left ventricular diastolic dysfunction
  4. Left ventricular ejection fraction ≥50%
  5. NT-pro BNP >125 pg/ml
  6. Signed study informed consent form

Inclusion criteria for HF-rEF group:

  1. Men and women aged ≥ 35 and <80 years
  2. Signs and symptoms of heart failure
  3. Left ventricular ejection fraction <50%
  4. Signed study informed consent form

Inclusion criteria for obstructive atherosclerosis group:

  1. Men and women aged ≥ 35 and <80 years
  2. Symptoms and signs of obstructive atherosclerosis of any vascular bed:

    1. Ischemic heart disease or
    2. Revascularization of coronary, renal, brachiocephalic or lower extremity arteries or
    3. carotid endarterectomy or
    4. chronic lower extremity ischemia or
    5. history of myocardial infarction, stroke, transient ischemic attack or
    6. renovascular AH
    7. atherosclerotic aorta aneurysm
  3. Signed study informed consent form

Inclusion criteria for control group for HF-pEF, HF-rEF and obstructive atherosclerosis

  1. Men and women aged ≥ 18 and <80 years.
  2. No signs or symptoms of chronic heart failure
  3. No signs of left ventricular diastolic dysfunction
  4. No history, signs or symptoms of obstructive atherosclerosis of any vascular bed
  5. Signed study informed consent form

Exclusion criteria for groups with HF-pEF, HF-rEF and obstructive atherosclerosis:

  1. Age <18 and ≥80 years.
  2. Refuse to sign study informed consent form
  3. Body mass index ≥35 kg/m2
  4. Chronic kidney disease with GFR <30 ml/min/1,73 m2
  5. Current smoking
  6. Moderate or severe COPD
  7. Moderate or severe asthma
  8. Acute infections or exacerbation of chronic infections 2 weeks prior to study enrollment
  9. History of allergic reactions to gadolinium contrast
  10. Hypertrophic cardiomyopathy, dilated cardiomyopathy, restrictive cardiomyopathy: primary, amyloidosis, glycogen storage diseases, hemochromatosis, sarcoidosis, drug induced cardiomyopathy, radiation heart disease, constrictive pericarditis).
  11. Connective tissue disease
  12. Cancer with no radical treatment
  13. Pregnancy or lactation
  14. Inflammatory bowel disease
  15. Use of antimicrobial agents, probiotics or systemic corticosteroids 3 months before the enrollment

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

Kohorter og intervensjoner

Gruppe / Kohort
Kontrollgruppe
Arterial hypertension
Atherosclerosis occlusive disease
Heart failure with preserved ejection fraction
Heart failure with reduced ejection fraction
Diabetes mellitus, type 2
Chronic obstructive pulmonary disease and asthma
Nonalcoholic fatty liver disease

Hva måler studien?

Primære resultatmål

Resultatmål
Tidsramme
Significant (p<0,05) correlation (r>0,5) between abundance of Faecalibacterium genus and concentration of lipopolysaccharide
Tidsramme: on enrollment
on enrollment

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart (Faktiske)

12. april 2021

Primær fullføring (Faktiske)

1. desember 2021

Studiet fullført (Faktiske)

1. desember 2021

Datoer for studieregistrering

Først innsendt

25. mars 2021

Først innsendt som oppfylte QC-kriteriene

25. mars 2021

Først lagt ut (Faktiske)

29. mars 2021

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

19. april 2022

Siste oppdatering sendt inn som oppfylte QC-kriteriene

18. april 2022

Sist bekreftet

1. april 2022

Mer informasjon

Begreper knyttet til denne studien

Plan for individuelle deltakerdata (IPD)

Planlegger du å dele individuelle deltakerdata (IPD)?

NEI

Legemiddel- og utstyrsinformasjon, studiedokumenter

Studerer et amerikansk FDA-regulert medikamentprodukt

Nei

Studerer et amerikansk FDA-regulert enhetsprodukt

Nei

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