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MEBO TMAU TESTING CURRENTLY SUSPENDED INDEFINITELY

MEBO - UBIOME study 2018

'PRESS RELEASE'

NCT03582826
ClinicalTrials.gov

MEBO Gut Microbiome Study
"Microbial Basis of Systemic Malodor and PATM Conditions (PATM)"
Funded by uBiome Research Grant

"Microbial Basis of Systemic Malodor and PATM Conditions (PATM)"

Dynamics of the Gut Microbiota in
Idiopathic Malodor Production
& PATM

Started May 2018 - Ongoing

Current people sent kits : 100/100
3 kits per person

NO LONGER RECRUITING

Participation info : LINK English

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Full details : https://goo.gl/TMw8xu
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TMAU UK end total:262
TMAU UK ends 23/01/20
TMAU Petition USA end total 204
USA : Moveon open
TMAU (Dominican)
Metabolomic Profiling Study
NCT02683876

Start : Aug 2016
Stage 1 : 27 Canadian volunteers to test
Latest click here (26 oct) :
17 samples returned


Note : Stage 1 is Canada only.
Return cut-off date : passed
Analysis can take 6/8 weeks
Analysis start in/before Nov
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MEBO Research Clinical Trials

Click here to read details of the MEBO Clinical Trials
NCT03582826 - Ongoing not recruiting
Microbial Basis of Systemic Malodor and PATM Conditions (PATM)
United States 2018 - ongoing

NCT02683876 - Completed
Exploratory Study of Relationships Between Malodor and Urine Metabolomics
Canada and United States 2016 - ongoing

NCT03451994 - Completed
Exploratory Study of Volatile Organic Compounds in Alveolar Breath
United Kingdom and United States 2013 - ongoing

NCT02692495 - Completed
Evaluation of Potential Screening Tools for Metabolic Body Odor and Halitosis
United Kingdom 2009 - 2012

Thursday, February 25, 2010

More about the ABCC11 gene that seems to cause natural hypohydrosis

Recently we posted about the ABCC11 gene, which seems to co-relate with naturally not being prone to underarm body odor (axillary odor). A sign of having the ABCC11 gene is that your earwax is the dry-type. This seems to be most common in far-east Asia. The following papers go into more detail about the gene. The hypothesis seems to be that it causes a natural hypohydrosis, which makes it more difficult for the axillary bacteria to thrive in the less moist environment. Although it is a 'loss of function' copy of the gene (a mutation), it is no surprise that in the communities where it first came about, now it has become the dominant type for that gene (e.g. mates have preferred those with the mutation. Now at levels of 95% of the communities.)

A functional ABCC11 allele is essential in the biochemical formation of human axillary odor

A strong association of axillary osmidrosis with the wet earwax type determined by genotyping of the ABCC11 gene

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