Investigation of the Effects of Different Levels of Obesity on the Respiratory System

February 13, 2022 updated by: alihan bilen, Istanbul Medipol University Hospital

Investigation of the Effects of Different Obesity Levels on the Respiratory System: In Our Study, Besides the Effect of Obesity on the Respiratory System, Many Different Parameters Related to Health Will be Compared.

Obesity can be defined as' a disease that occurs as a result of the energy (calorie) taken with food being more than the energy consumed and the excess energy being stored as fat in the body, negatively affecting the quality and duration of life. BMI is calculated by dividing the weight (kg) by the square of the height (m2) (1,2). According to the World Health Organization (WHO) classification, BMI between 25-29.9 kg / m2 is overweight, 30-34.9 kg / m2 is light, 35-39.9 kg / m2 is medium, 40 kg / m2 and above is considered as severe obesity. Obesity has important effects on respiratory function. These mechanical and biochemical effects are not easily measured by pulmonary function test and BMI measurement.Changes caused by mediators produced by adipose tissue likely cause changes in lung function, but this effect is not fully understood at the moment. The aim of our study is to make these effects more understandable and to compare them with different obesity classes and people with normal weight who are considered healthy.

Hypothesis 0: The effects of obesity on respiratory functions and multidimensional health-related parameters do not show a statistically significant difference compared to individuals with different levels of the disease and normal weight individuals classified as healthy.

Hypothesis 1: The effects of obesity on respiratory functions and multidimensional health-related parameters show a statistically significant difference compared to people with different levels of the disease and normal weight individuals classified as healthy.

The study will be carried out by face-to-face evaluations in a clinical setting with obese patients between the ages of 18-65 who have applied to the clinic with a diagnosis of obesity and agree to participate in the study, and healthy volunteers who are considered to be healthy without a diagnosis of obesity. Looking at the evaluations to be made; Measurement of respiratory function parameters, measurement of respiratory muscle strength, anthropometric measurements, evaluation of body composition, quality of life, upper extremity muscle strength and grip strength, lower extremity muscle strength, fatigue evaluation, vital signs, evaluation of exercise perception, presence of dyspnea and its level will be evaluated. A detailed description of these evaluations and the parameters to be used will be explained in detail in the next step.

Study Overview

Detailed Description

Obesity can be defined as' a disease that occurs as a result of the energy (calorie) taken with food being more than the energy consumed and the excess energy being stored as fat in the body, negatively affecting the quality and duration of life. A body mass index (BMI) of 30 or above in adults is classified as obese. BMI is calculated by dividing the weight (kg) by the square of the height (m2). According to the World Health Organization (WHO) classification, BMI between 25-29. 9 kg / m2 is overweight, 30-34. 9 kg / m2 is light, 35-39. 9 kg / m2 is medium, 40 kg / m2 and above is considered as severe obesity. As the increases in BMI are related to the number of comorbidities, weight loss also affects many risk factors. It has been shown that voluntary weight loss in obese individuals over short periods (weeks or months) reduces risk factors and improves disease symptoms associated with obesity, including heart disease, Type II Diabetes mellitus, and osteoarthritis. Obesity; It is an important risk factor and disease factor for asthma, obstructive sleep apnea syndrome, obesity hypoventilation syndrome (OHS) and pulmonary hypertension diseases. The overall effect of obesity on lung function is multifactorial and is related to the mechanical and inflammatory aspects of obesity. Obesity has important effects on respiratory function. These mechanical and biochemical effects are not easily measured by pulmonary function test and BMI measurement. Changes caused by mediators produced by adipose tissue likely cause changes in lung function, but this effect is not fully understood at the moment.As a result of the literature review the investigators conducted, it was observed that the studies conducted in order to make more understandable the physiological and mechanical effects of obesity on different systems in the body, especially the respiratory system, were limited and inadequate in terms of numerical and targeted purposes. It was observed that lower extremity muscle strength, fatigue, sleep quality parameters were not included, and their relations with respiratory system functions and measurements were not measured. The aim of our study is to make these effects more understandable and to compare them with different obesity classes and people with normal weight who are considered healthy. Individuals who volunteered to participate in the study, who met the inclusion criteria and volunteered to participate will be evaluated by dividing them into five different groups according to the BMI parameter, in accordance with the intervals determined by WHO, and the data obtained will be compared between the groups.

Outcome Measures:

  • Measurement of Pulmonary Function Parameters: The respiratory function parameters of the participants will be measured with a respiratory function test using a spirometer. With these tests, the static and dynamic lung volumes and functional status of the person will be determined.
  • Measurement of Respiratory Muscle Strength:

It consists of respiratory muscles, diaphragm, intercostal (internal and external), scalene, sternocleidomastoid, triangularis sterni, abdominal, shoulder and neck muscles. Respiratory muscle strength can be measured in many different ways. Among the pulmonary function tests, maximum inspiratory and expiratory pressures are the measurements that are frequently used to evaluate the strength of the respiratory muscles. -Measurement of Respiratory Muscle Strength:It consists of respiratory muscles, diaphragm, intercostal (internal and external), scalene, sternocleidomastoid, triangularis sterni, abdominal, shoulder and neck muscles. Respiratory muscle strength can be measured in many different ways. Among the pulmonary function tests, maximum inspiratory and expiratory pressures are the measurements that are frequently used to evaluate the strength of the respiratory muscles. These measurements are directly related to respiratory muscle strength and help to determine the rehabilitation and exercise program by providing information about the patient's condition.

-Anthropometric Measurements: Participants' waist circumference, hip circumference, neck circumference will be measured, and their ratios (waist / height ratio, waist / hip ratio) will be calculated. Body mass index (BMI), waist circumference, and waist-to-hip ratio (B / C) is the diagnostic methods commonly used to detect adiposity. Waist circumference and waist-hip ratio have been found to be useful measurements for measuring visceral fat accumulation. Measurement of neck circumference is used as an anthropometric marker to identify patients at risk for sleep apnea syndrome. At the same time, neck circumference is thought to be associated with other metabolic diseases. In addition to these measurements, the measurement called 'New BMI' used in the literature will also be made. In this measurement, BMI is calculated with the formula 1.3 × (kg / m2).

In order to calculate the body fat ratio, it is aimed to estimate the amount of body fat with the measurement of Clinica Universidad de Navarra-Body Adiposity Estimator (CUN-BAE) in addition to the bioelectric impedance method.

BMI measurement is insufficient to determine body fat and muscle ratio. Since it is difficult to determine the location of the fat tissue in the body, it will be evaluated with the '' Body Shape Index ''.

-Assessment of Body Composition: Body composition will be measured using the method called bioelectrical impedance analysis (BIA). This measurement is based on the principles of electrical conductivity of body tissues. It is a fast, practical and relatively inexpensive method compared to other similar devices and applications used to examine the body composition of individuals. This method shows the percentage and mass of body fat, lean body weight and the amount of water in the body and their distribution percentage. The person climbs on the device and places his or her hands in the designated places. Electric current travels through the body and provides information about parameters determined by certain algorithms and calculations.

-Quality of Life: Quality of life is accepted as a multidimensional structure with many different contents. Considering the decrease in physical capacity, pain, deterioration in interpersonal relationships, decreased self-esteem, loss of self-esteem, depression, social stigma, difficulty in finding a job, rejection by the school and business environment, it is understood how low the health-related quality of life of obese individuals is. In measuring the quality of life; Nottingham Health Profile questionnaire will be used. Nottingham Health Profile is a questionnaire consisting of 7 subtitles and 45 questions, including physical, social and psychological evaluations.

-Upper Extremity Muscle Strength and Gripping Strength: It is an important parameter related to muscle strength, functional capacity, cardiovascular disease risk factors and mortality. Upper extremity muscle strength and grip strength will be measured by hand dynamometer and weight lifting tests (arm curls test).

-Lower Extremity Muscle Strength: Abnormalities that usually occur in lower extremity muscles affect patients' physical performance and daily living activities, reduce exercise tolerance and impair health-related quality of life. 30-second sit-and-go test will be used to measure lower extremity muscle strength. The score is determined by the number of times the participant sits and stands up for 30 seconds from the moment the participant is commanded to place his hands on the crossed, shoulders in the chair he is sitting with his back supported and to start in the position where his feet are in full contact with the floor.

  • Fatigue Assessment:

Fatigue is a common complaint in overweight and obese people. It has been stated that this is caused by increased body mass, decreased physical activity level and sleep disorders. In the assessment of fatigue, the Fatigue Severity Scale (39) will be used. The fatigue severity scale consists of 9 questions that question social relationship, physical performance and symptomatically the severity of fatigue. The total score is created according to the answers given to the questions.

-Vital Sign: Type 2 diabetes mellitus (T2DM), hypertension (HT), dyslipidemia (DLP), obstructive sleep apnea syndrome (OSAS) comorbidities have been associated with morbid obesity in obese individuals. Blood pressure, heart rate, oxygen saturation will be evaluated in order to observe the negative effects of these comorbidities.

-Evaluation of Exercise Perception: Aerobic exercise capacity is an essential component of physical fitness. Perceived benefits and perceived barriers to participating in physical activity will be assessed by Exercise Benefits / Barriers Scale (EBBS). It is a questionnaire consisting of 43 questions used to evaluate people's perception of exercise. Evaluates the ideas of being useful and preventive that exercise creates on people. The test score is determined by the score collected according to the answers given to the questions.

-Assessment of the Presence and Level of Dyspnea: According to the American Thoracic Society (ATS) report, the definition of dyspnea was defined as "unpleasant or uncomfortable breathing sensation and personal respiratory disturbance caused by various intensity senses" and it was stated to be a subjective feeling. "Modified Medical Research Council Scale (MMRC)" will be used to evaluate the presence of dyspnea. The MMRC is a five-item scale created on the basis of various activities that cause shortness of breath. The presence and effect of dyspnea occur according to the substance chosen by the person.

-Statistical method (s) to use: '' Hatem AM, Ismail MS, El-Hinnawy YH. 'Effect of different classes of obesity on the pulmonary functions among adult Egyptians: a cross-sectional study', Egypt J Bronchol 2019; 13: 510-5 '', the total number of samples determined for 5 groups in the sample size study, based on the FVC value and standard deviations in table 2, was calculated as 80 on the condition that it was 16 per group. Sample size calculation was made using the NCSS / PASS program. In the calculation, it was determined that the difference between the averages of the 5 groups should be 80% power and 95% confidence level to be significant. The statistical test method to be applied ANOVA will be used in conditions of normal distribution between groups, and Kruskal-Wallis test method will be used if the condition of normal distribution between groups cannot be achieved.

Study Type

Observational

Enrollment (Actual)

100

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Istanbul, Turkey, 34098
        • Istanbul University-Cerrahpaşa Faculty of Medicine Internal Medicine Department of Endocrinology and Metabolic Diseases

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 65 years (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

According to the WHO classification, the five groups to be formed will be group I normal weight (healthy), group II overweight, group III, class 1 obese, group IV, class 2 obese, group V, class 3 (morbid) obese.

Description

Inclusion Criteria:

  • Being in the age range of 18-65,
  • body mass index ≥18.5 according to the World Health Organization (WHO) classification,
  • Volunteering to participate in the study,

Exclusion Criteria:

  • Accompanying neurological or orthopedic effects that will prevent participation in the study,
  • Pregnancy status,
  • Presence of a pacemaker,
  • Having had Covid-19 disease ,
  • Having had any thoracic or abdominal surgery or injury,
  • For evaluation and control purposes Being unable to understand and apply the tests to be applied mentally and physically successfully,

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
GROUP I
Group I will include cases classified as normal weight (healthy) with a body mass index of 18.5-24.9 kg / m2 as a result of the classification made by the World Health Organization. All parameter and evaluation measurements determined for this group will be made. Since this group was not considered as obese, it was determined as the control group.
GROUP II
Group II will include cases classified as overweight and having a body mass index of 25.0-29.9 kg / m2 as a result of the classification made by the World Health Organization. All parameter and evaluation measurements determined in this group will be made.
GROUP III
Group III will include cases classified as class I obese, with a body mass index of 30.0-34.9 kg / m2 as a result of the classification made by the World Health Organization. All parameter and evaluation measurements determined in this group will be made.
GROUP IV
Group IV will include cases classified as class II obese, with a body mass index of 35.0-39.9 kg / m2 as a result of the classification made by the World Health Organization. All parameter and evaluation measurements determined in this group will be made.
GROUP V
Group V will include cases classified as class III (morbid) obese, with a body mass index of 40 kg / m2 as a result of the classification made by the World Health Organization. All parameter and evaluation measurements determined in this group will be made.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Respiratory Function Parameters
Time Frame: Day 1.
The respiratory function parameters of the participants will be measured with a pulmonary function test using a spirometer. With these tests, the static and dynamic lung volumes and functional status of the person will be determined. Spirometric measurements will be carried out by applying the guidelines for standardization of pulmonary function tests prepared by the American Thoracic Society (ATS) and the European Respiratory Society (ERS).
Day 1.

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Respiratory Muscle Strength
Time Frame: Day 1.
Respiratory muscles are composed of diaphragm, intercostal (internal and external), scalene, sternocleidomastoid, triangularis sterni, abdominal, shoulder and neck muscles. Respiratory muscle strength can be measured in many different ways. The maximum inspiratory and expiratory pressures among the respiratory function tests are the measurements that are frequently used to evaluate the strength of the respiratory muscles. These measurements are directly related to respiratory muscle strengths and assist in determining the rehabilitation and exercise program by providing information about the patient's condition. Respiratory muscle strength measurements will be carried out in accordance with the standardization of the guidelines prepared by the American Thoracic Society (ATS) and the European Respiratory Society (ERS).
Day 1.
Measurement of Quality of Life
Time Frame: Day 1.
Quality of life is accepted as a multidimensional structure with many different contents . In the measurement of quality of life; ''Nottingham Health Profile'' questionnaire will be used. Nottingham Health Profile is a questionnaire consisting of 7 subtitles and 45 questions including physical, social and psychological evaluations. This multifaceted scale includes: pain, emotional reactions, sleep, physical activity, energy and health status
Day 1.
Perception Of Exercise
Time Frame: Day 1.
Aerobic exercise capacity is an essential component of physical fitness. Perceived benefits and perceived barriers to participating in physical activity will be assessed through the Exercise Benefits / Barriers Scale This scale consists of 43 multiple-choice questions. According to the answers given, the minimum score that can be taken is 43 and the maximum score is 172. The higher the score, the better the perception of people about exercise..
Day 1.

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
Anthropometric Measurements Ratios
Time Frame: Day 1.
Measuring the waist circumference, hip circumference and neck circumference and their ratios (waist / height ratio, waist / hip ratio) to each other will be calculated. Anthropometric measurements (height, weight, waist, neck and hip circumference) will be carried out according to the World Health Organization (WHO) measurement criteria. Measurements will be made with a 150 centimeter long tape measure that is not rigid.
Day 1.
Neck Circumference
Time Frame: Day 1.
Measurement of neck circumference is used as an anthropometric marker to identify patients at risk for sleep apnea syndrome. Anthropometric measurements will be carried out according to the World Health Organization (WHO) measurement criteria. Measurements will be made with a 150 centimeter long tape measure that is not rigid.
Day 1.
Waist Circumference
Time Frame: Day 1.
Waist circumference has been found to be useful measurements for measuring visceral fat accumulation. waist circumference is a frequently used diagnostic method for detecting adiposity. Waist circumference has been found to be useful measurements for measuring visceral fat accumulation. Anthropometric measurements will be carried out according to the World Health Organization (WHO) measurement criteria. Measurements will be made with a 150 centimeter long tape measure that is not rigid.
Day 1.
NEW BMI
Time Frame: Day 1.
A measurement called 'New BMI' used in the literature will also be made. In this measurement, BMI is calculated with the formula 1.3 × (kg / m2).
Day 1.
Assessing Body Composition
Time Frame: Day 1.
Body composition will be measured using the method called bioelectrical impedance analysis (BIA). With the device used in this method, the weight and height of the people are also measured. This measurement is based on the principles of electrical conductivity of body tissues. It is a fast, practical and relatively inexpensive method compared to other similar devices and applications used to examine the body composition of individuals. This method shows the percentage and mass of body fat, lean body weight and the amount of water in the body and their distribution percentage.
Day 1.
Body Adiposity Estimator
Time Frame: Day 1.
In order to calculate the body fat ratio, it is aimed to estimate the amount of body fat with the measurement of Clinica Universidad de Navarra-Body Adiposity Estimator (CUN-BAE) in addition to the bioelectric impedance method. In this measurement,% BF (Percent estimate of body fat) = -44.988 (0.503 × age) (10.689 × gender) (3.172 × BMI) - (0.026 × BMI) (0.181 × BMI × gender) - (0.02 × BMI × age ) - (0.005 × BMI2 × gender) (0.00021 × BMI2 × age) (The multiplier value for the female gender is determined as 1, for the male gender the multiplier value is determined as 0)
Day 1.
Body Shape Index
Time Frame: Day 1.
BMI measurement is insufficient to determine body fat and muscle ratio. Since it is difficult to determine the location of the fat tissue in the body, it will be evaluated with the "Body Shape Index" in this regard. Body Shape Index is calculated with the formula waist circumference (cm) / (BMI2 / 3 × Height (m) 1/2).
Day 1.
Body Adiposity Index
Time Frame: Day 1.
Another parameter used to determine the body fat percentage is called the "Body Adiposity Index". A predictive value for the percentage of body fat is determined by the measurement result. Body Adiposity Index is calculated with the formula (hip circumference / Height (m) 1.5) -18.
Day 1.
Upper Extremity Muscle Strength
Time Frame: Day 1.
In the weight lifting test to be used to measure upper extremity muscle strength, the score is determined by bringing the arm to full extension from the person (3.60 kg for male participants, 2.3 kg for female participants) and the number of full lifts for 30 seconds.In the weightlifting test to be used to measure upper extremity muscle strength, the score is determined by bringing the arm to full extension of the person (3.60 kg for male participants, 2.3 kg for female participants) and the number of full lifts for 30 seconds.
Day 1.
Gripping Strength
Time Frame: Day 1.
Grip strength measurement is made using a hand dynamometer to measure the grip strength of the hand isometric.
Day 1.
Lower Extremity Muscle Strength
Time Frame: Day 1.
Abnormalities that usually occur in lower extremity muscles affect patients' physical performance and activities of daily living, reduce exercise tolerance and impair health-related quality of life. 30-second sit-and-go test will be used to measure lower extremity muscle strength. The score is determined by the number of times the participant sits and stands up for 30 seconds from the moment the participant is commanded to place his hands on the crossed shoulders in the chair he is sitting with his back supported and to start in the position where his feet touch the floor.
Day 1.
Fatigue Assessment
Time Frame: Day 1.
The fatigue severity scale consists of 9 questions that question social relationship, physical performance and symptomatically the severity of fatigue. The total score is created according to the answers given to the questions.The questions are scored between 0 and 7, and the result is obtained by dividing the total score by nine. As the total score increases, the severity of fatigue increases. If the result is less than 2.8, the result is found with no fatigue. If it is greater than 6.1, it is considered as chronic fatigue.
Day 1.
Blood Pressure
Time Frame: Day 1.
Central adiposity has long been linked to hypertension in adults, with the finding that cardiovascular and metabolic complications of obesity were more common in patients with the upper body obesity phenotype. Blood pressure will be measured with a digital sphygmomanometer
Day 1.
Heart Rate
Time Frame: Day 1.
Another important manifestation of obesity is impairment in the autonomic nervous system, present in all age groups, each of which has its own profile. Heart rate also changes due to this influence. Heart rate obtained using a heart rate monitor.
Day 1.
Oxygen Saturation
Time Frame: Day 1.
Oxygen saturation is an important vital parameter. Oxygen saturation will be measured with a pulse oximeter.
Day 1.
Evaluation of the Presence and Level of Dyspnea
Time Frame: Day 1.
According to the report of the American Thoracic Society (ATS), the definition of dyspnea was defined as "unpleasant or uncomfortable breathing sensation and personal respiratory distress caused by various intensity sensations '' and it was stated to be a subjective feeling. "Modified Medical Research Council Scale " will be used to evaluate the presence of dyspnea. The scale is a five-item scale based on various activities that cause shortness of breath. The presence and effect of dyspnea occurs according to the substance chosen by the person. In this scale consisting of five options, the effect created by the presence of dyspnea is determined according to the answer given. The lowest score is 0, the highest score is 5. Higher score means more exposure. And the higher the score, the worse the result.
Day 1.

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Collaborators

Investigators

  • Study Director: Gülay Aras Bayram, Phd, Medipol University

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

March 1, 2020

Primary Completion (Actual)

December 24, 2021

Study Completion (Actual)

December 24, 2021

Study Registration Dates

First Submitted

February 23, 2021

First Submitted That Met QC Criteria

March 2, 2021

First Posted (Actual)

March 4, 2021

Study Record Updates

Last Update Posted (Actual)

February 15, 2022

Last Update Submitted That Met QC Criteria

February 13, 2022

Last Verified

February 1, 2022

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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