Obesity Clinical Trial
Official title:
Study on Dietary Nutrition Intervention Techniques for Children Obesity
With the rapid development of society and economy, children's simple obesity is the rising in
the world and has become a chronic disease which is one of the biggest public health
challenges in the world. It is a serious threat to the health of children and their
adulthood. The overweight and obesity is induced by the genetic and environmental factors.
The environmental factors are very important, while the dietary factors are the driving
factors of many chronic diseases including obesity. This study focus on the dietary
intervention of childhood obesity to build healthy intestinal flora. The interventing food
was based on a natural health food - fruit and vegetable fermentation liquid, and combined
with other probiotic dietary factors, dietary fiber and oligosaccharides. The implementation
of the study will help to reveal the fuction mechanism of intestinal bacteria in the obese
children and normal children, and to construct healthy micro environment of intestinal flor.
According to the positive effect factors, the study will propose a healthy diet and nutrition
intervention model for obese children, which is significant to social health especially to
children's health.
To investigate the accuracy of MRI in quantifying liver fat with magnetic resonance
spectroscopy (MRS) as a reference. A secondary goal was to assess the prevalence of
nonalcoholic fatty liver disease in overweight and obese Chinese children and adolescents.
Before academic examination, letter to parents, informed consent and volunteer questionnaire
are released to school children and their guardians. We tell the volunteers and their
guardians what about this study and invite them to participate this study. Only the
volunteers and guardians signature on the letter to parents and informed consent are able to
the research objects.
Experimental procedures:
Two times of medical exams, blood and stool sample collection is required for the whole
experiment research. The first time exams and sample collection is carried on during academic
examination; the second time is carried on after the intervention.
Recruit of research objects:
According to academic examination and volunteer questionnaires, about 300 healthy children
without in taking antibiotics before 3 months are recruited and their BMI should be in the
obese range. Then their waist circumference and the ratio of body fat are measured. If the
ratio of waist size to weight of them is >0.46 and they have higher percentage of body fat
(>20% for boys and under 12 years old girls, >25% for 12 years old girls), the data are
collected and input to the database. About 40 healthy children between 15-18 years old are
recruited to participate the next intervention research.
General body examination:
In academic examination, the student's basic medical data including height and weight are
recorded, and then their BMI are calculated. If his/her BMI are in the obese range, his/her
body composition are measured and recorded.
MRI and MRS test:
All patients underwent MRI scanning performed by an experienced technologist using a 3 Tesla
MR unit (MAGNETOM Skyra, Siemens Healthcare, Erlangen, Germany). MRI and MRS were performed
with multi-echo Dixon and HISTO sequences, respectively, to calculate hepatic proton density
fat fraction (PDFF).
Blood collection, preservation and test:
Blood collection and preservation are proceed in standard of medical examination. When
collecting the data of obesity, the tests of blood count, blood glucose, serum lipid and
liver function should be processed for obese children. When intervening, more tests including
blood count, blood glucose, blood lipids, liver function, hemoglobin, cytokines, insulin,
high sensitivity C-reactive protein, leptin and somatomedin C should be processed.
Stool collection, preservation and detection:
50 ml centrifuge tubes are used to collect stool samples. Each tube is marked a unique
encoding corresponds to a volunteer. When volunteers collecting stool samples, they transfer
the stool samples into sterile centrifuge tube using sterile swabs or toothpicks as soon as
possible. The collecting samples should be more than 10g. The centrifuge tubes should be put
in low-temperature place , then transfer to refrigerator and stored at -80 ℃ until to DNA
extraction and other testing. The tests including short chain fatty acids content (SCFA), pH,
water content, immune factors sIgA and Calprotectin are processed.
16S rRNA gene sequencing of bacteria in stools:
DNA extraction:
For each sample, about 0.2g stool is weighted and the total DNA is extracted using fecal
genomic DNA extraction Kit (Qiagen, model DP328). And then the concentration and purity of
extracted DNA were measured using NanoDrop (Thermo, 2000C) to guarantee each sample meets the
sequencing requirement.
Sample sequencing:
PCR amplification of 16S rRNA gene (V3-V4) are performed with universal forward primers
5'-ACTCCTACGGGAGGCAGCAG-3' and reverse primer 5'-GGACTACVSGGGTATCTAAT-3'. The amplification
system include sterile water 19.375 ul, buffer 2.5ul, template 1ul, primers 1ul, Pyrobest DNA
polymerase 0.125ul. PCR cycling conditions were as follows: 94 ℃ 5min, followed by some
cycles including 94℃ denaturing for 30s, 50℃ renaturing for 30s,72℃ extending for 30s, then
72℃ extending for 5min. PCR product electrophoresis are performed to determine the
appropriate PCR product with different application cycles. After connecting amplified
products to tagged primers and labels, paired-end sequencing are performed with the
sequencing platform of Illumina MiSeq, and the read length is about 250bp.
Intervention treatment on childhood obesity with PFE:
After 16S rRNA gene sequencing, about 40 obese volunteers in high school and with similar
intestinal flora profiles are selected to participate the intervention treatment research.
The intervening food is "Dr. Ephraim" plant fermentation extract (PFE). Without changing the
previous diets of research objects, each research object drinks drinking 30mL PFE at morning
and evening enzymes respectively, and the intervention last for 8 weeks. Before and after
8-week intervention, stool and blood samples of research objects are collected and analyzed
to obtain their physiological and biochemical indexes. The all 16S rRNA gene of fecal samples
in each stage are sequenced.
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