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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05156255
Other study ID # 21-08-0852
Secondary ID
Status Completed
Phase
First received
Last updated
Start date December 1, 2021
Est. completion date April 14, 2023

Study information

Verified date September 2023
Source Indonesia University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Human milk oligosaccharides (HMOs), the third most abundant constituent of breastmilk, are known to have beneficial effects on infant immunity. Maternal genetic polymorphisms cause HMO variability. The FUT2 gene determines the secretor status, whereas the FUT3 gene is responsible for the expression of Lewis fucosyltransferase. Therefore, breastmilk can be classified to four groups according to the variation. To date, this variability has not been investigated in Indonesia. This study aims to evaluate the association between FUT2 gene polymorphism and 2'-Fucosyllactose (2'-FL) secretor phenotype. In addition, infant FUT2 gene polymorphism and short chain fatty acid (SCFA) profile from stool samples are also analysed.


Description:

Eligible mother-infant pairs are explained about this study. Those willing to participate in this study are asked for written informed consent. Mothers are interviewed about their baseline characteristics, family pedigree, nutritional intake, and routine drug consumption. Infants are checked for their birth history. Both are measured for weight and height. Four specimens are collected from the subjects: 1. Mother 1. Breastmilk Breastmilk is expressed at 8-11 AM to avoid variability due to circadian rhythm. One breast is emptied, 30 mL of breastmilk is stored in a sterile container, and the rest is returned for feeding. Breastmilk is divided to five 2-mL cryovials and stored in a -80°C freezer. The remaining is stored in a -20°C freezer. 2. Blood Blood samples (3 mL) are collected for DNA extraction. 2. Infant 1. Buccal cells Buccal swab kits are used to obtain samples for DNA extraction. 2. Stool Stool specimens are collected at the age of four weeks in a sterile container and stored in a -80°C storage before short chain fatty acid profile analysis.


Recruitment information / eligibility

Status Completed
Enrollment 120
Est. completion date April 14, 2023
Est. primary completion date July 31, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 2 Weeks and older
Eligibility Inclusion Criteria: - Mother 1. Minimum of 18 years old 2. With term infants aged 2-5 weeks 3. Exclusively breastfeed 4. Healthy condition 5. Agree to participate and sign the informed consent - Infant 1. Infant with mother who fulfil the eligibility criteria Exclusion Criteria: - Mother 1. Has a Caucasian ancestor in two generations above 2. Infant has multiple congenital anomalies - Infant 1. Has ever received antibiotics

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Indonesia Faculty of Medicine, Universitas Indonesia Jakarta Pusat DKI Jakarta

Sponsors (2)

Lead Sponsor Collaborator
Indonesia University University Medical Center Groningen

Country where clinical trial is conducted

Indonesia, 

Outcome

Type Measure Description Time frame Safety issue
Primary Human milk oligosaccharides profile of Indonesian mothers The concentration of 19 HMOs will be measured using high performance anion exhange chromatography with pulsed amperometric detection (HPAEC-PAD). 1 day
Primary Proportion of FUT2 secretor genotype of mothers based on single nucleotide polymorphism (SNP) rs601338 Sequencing of coding sequence (exon 2) of FUT2 gene will be performed using a previously known outer primer from the study by Lefebvre, et al (2020). The results will be aligned with database from www.ncbi.nlm.nih.gov to find the proportion of rs601338 among mothers. 1 day
Primary Association between rs601338 FUT2 secretor genotype and 2'-FL secretor phenotype in mothers The association between rs601338 FUT2 genotype (homozygous dominant, heterozygous, homozygous recessive) and 2'-FL concentration will be analysed using ANOVA test. 1 day
Secondary Novel FUT2 polymorphism in Indonesian mothers The sequencing result of exon 2 in the FUT2 gene will be aligned with database from www.ncbi.nlm.nih.gov to find novel variants. Additional information regarding existing variants will be browsed using the same database. The allele frequency of new variants will be calculated to determine new SNP. 1 day
Secondary Proportion of FUT2 secretor genotype of infants based on single nucleotide polymorphism (SNP) rs601338 Sequencing of coding sequence (exon 2) of FUT2 gene will be performed using a previously known outer primer from the study by Lefebvre, et al (2020). The results will be aligned with database from www.ncbi.nlm.nih.gov to find the proportion of rs601338 among infants. 1 day
Secondary Novel FUT2 polymorphism in infant The sequencing result of exon 2 FUT2 will be aligned with database from www.ncbi.nlm.nih.gov to find novel variants. Additional information regarding existing variants will be browsed using the same database. The allele frequency of new variants will be calculated to determine new SNP. 1 day
Secondary Profile of infant stool short chain fatty acid based on mother-infant FUT2 genotype pairs The concentration of total short chain fatty acid, acetate, propionate, and butyrate in infant's stool will be measured using gas chromatography-mass spectrometry (GC-MS). Difference in the concentration between four mother-infant genotype pairs will be analysed using ANOVA test. 1 day
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