This study aims to evaluate the changes in metabolic parameters, intestinal permeability, and gastrointestinal symptoms in individuals who have undergone bariatric surgery (Laparoscopic Sleeve Gastrectomy - LSG) for obesity treatment. Obesity is a chronic disease associated with serious health complications including type 2 diabetes, hypertension, cardiovascular disease, and metabolic disorders. Bariatric surgery is currently the most effective treatment method for morbid obesity. However, monitoring patients after surgery in terms of metabolic health, gut permeability, and gastrointestinal symptoms is crucial for long-term success. In this study, 40 volunteers (aged 19-50) who have undergone LSG surgery within the last month will be followed for 6 months. At the beginning of the study and 6 months later, the following will be assessed: * Metabolic parameters: fasting blood glucose, total cholesterol, triglycerides, high-density lipoprotein (HDL), low-density lipoprotein (LDL), very low-density lipoprotein (VLDL) cholesterol, and insulin levels * Intestinal permeability markers: zonulin, secretory immunoglobulin A (IgA), and lipopolysaccharide (LPS) levels * Gastrointestinal symptoms: assessed using the Gastrointestinal Symptom Rating Scale (GSRS) * Anthropometric measurements: body weight, height, waist and hip circumference, BMI * Nutritional intake: 3-day dietary records The study will be conducted at Bursa Yıldırım Doruk Hospital, General Surgery Clinic. Results will contribute to understanding the relationship between bariatric surgery and gut health, potentially helping to prevent postoperative complications.
Obesity is defined by the World Health Organization (WHO) as abnormal or excessive fat accumulation that presents a risk to health. Bariatric surgery, particularly Laparoscopic Sleeve Gastrectomy (LSG), is considered the most effective long-term treatment for morbid obesity. This prospective observational study will be conducted at Bursa Yıldırım Doruk Hospital with 40 volunteers who have undergone LSG within the last month. Participants will be evaluated at baseline (immediately after surgery) and at 6 months post-surgery. Assessments include: 1. Anthropometric Measurements: Body weight, height, waist and hip circumference will be measured. BMI and waist-to-hip ratio will be calculated according to WHO criteria. 2. Biochemical Parameters: Fasting blood glucose, total cholesterol, triglycerides, high-density lipoprotein (HDL), low-density lipoprotein (LDL), very low-density lipoprotein (VLDL) cholesterol, and insulin levels will be obtained from patient records. Zonulin, secretory immunoglobulin A (IgA), and lipopolysaccharide (LPS) levels will be analyzed using ELISA method (Biotek TS800) with commercial kits (RelAssay® Diagnostics, Ankara, Turkey) at Ankara Diagen Laboratory. Samples will be stored at -20°C until analysis. 3. Gastrointestinal Symptom Rating Scale (GSRS): A validated 15-item scale assessing five dimensions: diarrhea, indigestion, constipation, abdominal pain, and reflux. Scores range from 1 (no discomfort) to 7 (very severe discomfort). Turkish validity and reliability was established by Turan and Asti (2011). 4. Dietary Assessment: 3-day dietary records will be collected and analyzed using the Nutrition Information System (BeBIS) 8.2 software. Results will be evaluated according to the Turkish Dietary Guidelines 2022 (TUBER 2022). Statistical analyses will be performed using the Statistical Package for the Social Sciences (SPSS) 22.0. Normal distribution will be assessed using Kolmogorov-Smirnov/Shapiro-Wilk tests. Results will be expressed as mean ± standard deviation for continuous variables and frequency/percentage for categorical variables.
Study Type
OBSERVATIONAL
Enrollment
40
Participants will undergo two assessment visits: at baseline (within 1 month post-surgery) and at 6-month follow-up. Each visit includes anthropometric measurements (body weight, height, waist and hip circumference, BMI), biochemical blood analysis (fasting glucose, lipid profile, insulin, zonulin, secretory IgA, LPS), gastrointestinal symptom evaluation via GSRS, and 3-day dietary records.
Bursa Yıldırım Doruk Hospital
Bursa, Bursa, Turkey (Türkiye)
Change in Fasting Blood Glucose Concentration (mg/dL)
Change in serum fasting blood glucose levels after 12-hour fasting between baseline and 6-month follow-up.
Time frame: Baseline and 6 months
Change in Total Cholesterol Concentration (mg/dL)
Change in serum total cholesterol levels after 12-hour fasting between baseline and 6-month follow-up.
Time frame: Baseline and 6 months
Change in Triglyceride Concentration (mg/dL)
Change in serum triglyceride levels after 12-hour fasting between baseline and 6-month follow-up.
Time frame: Baseline and 6 months
Change in HDL Cholesterol Concentration (mg/dL)
Change in serum high-density lipoprotein (HDL) cholesterol levels after 12-hour fasting between baseline and 6-month follow-up.
Time frame: Baseline and 6 months
Change in LDL Cholesterol Concentration (mg/dL)
Change in serum low-density lipoprotein (LDL) cholesterol levels after 12-hour fasting between baseline and 6-month follow-up.
Time frame: Baseline and 6 months
Change in VLDL Cholesterol Concentration (mg/dL)
Change in serum very low-density lipoprotein (VLDL) cholesterol levels after 12-hour fasting between baseline and 6-month follow-up.
Time frame: Baseline and 6 months
Change in Fasting Insulin Concentration (µIU/mL)
Change in serum fasting insulin levels after 12-hour fasting between baseline and 6-month follow-up.
Time frame: Baseline and 6 months
Change in Serum Zonulin Concentration (ng/mL)
Change in serum zonulin levels assessed by ELISA method between baseline and 6-month follow-up.
Time frame: Baseline and 6 months
Change in Serum Secretory IgA Concentration (mg/dL)
Change in serum secretory IgA levels assessed by ELISA method between baseline and 6-month follow-up.
Time frame: Baseline and 6 months
Change in Serum LPS Concentration (EU/mL)
Change in serum lipopolysaccharide (LPS) levels assessed by ELISA method between baseline and 6-month follow-up.
Time frame: Baseline and 6 months
Change in Gastrointestinal Symptom Rating Scale (GSRS) Total Score (1-7)
Change in total score of the Gastrointestinal Symptom Rating Scale (GSRS) between baseline and 6-month follow-up. The scale consists of 15 items across 5 subscales; scores range from 1 to 7, with higher scores indicating more severe gastrointestinal symptoms.
Time frame: Baseline and 6 months
Change in Body Weight (kg)
Change in body weight between baseline and 6-month follow-up.
Time frame: Baseline and 6 months
Change in Body Mass Index (kg/m²)
Change in BMI between baseline and 6-month follow-up. Weight and height will be combined to report BMI in kg/m².
Time frame: Baseline and 6 months
Change in Waist Circumference (cm)
Change in waist circumference between baseline and 6-month follow-up.
Time frame: Baseline and 6 months
Change in Hip Circumference (cm)
Change in hip circumference between baseline and 6-month follow-up.
Time frame: Baseline and 6 months
Change in Waist-to-Hip Ratio
Change in waist-to-hip ratio between baseline and 6-month follow-up. Waist and hip circumference measurements will be combined to calculate the waist-to-hip ratio.
Time frame: Baseline and 6 months
Change in Daily Energy Intake (kcal/day)
Change in daily energy intake assessed by 3-day dietary intake records between baseline and 6-month follow-up. Data will be analyzed using BeBIS 8.2 software.
Time frame: Baseline and 6 months
Change in Daily Protein Intake (g/day)
Change in daily protein intake assessed by 3-day dietary intake records between baseline and 6-month follow-up. Data will be analyzed using BeBIS 8.2 software.
Time frame: Baseline and 6 months
Change in Daily Carbohydrate Intake (g/day)
Change in daily carbohydrate intake assessed by 3-day dietary intake records between baseline and 6-month follow-up. Data will be analyzed using BeBIS 8.2 software.
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Time frame: Baseline and 6 months
Change in Daily Fat Intake (g/day)
Change in daily fat intake assessed by 3-day dietary intake records between baseline and 6-month follow-up. Data will be analyzed using BeBIS 8.2 software.
Time frame: Baseline and 6 months