ID

45898

Descripción

Principal Investigator: Julie A. Mennella, Monell Chemical Senses Center MeSH: Taste Perception,Sensation https://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?study_id=phs000839 The goal of this project is to determine variation in human bitter perception and the effectiveness of bitter blockers in individuals of different genotypes. The project is based on the parent project titled "Efficacy of bitter taste blockers on flavor acceptance in pediatric population", which addresses how bitter taste perception affects medication compliance. As a part of the parent project, mothers and their children were recruited from the general population of metropolitan Philadelphia through print and internet media as well as from a database of past research participants. Adults (mothers) were evaluated in the laboratory for bitter taste perception for a variety of "Generally Recognized As Safe" (GRAS) bitter compounds using the general Labeled Magnitude Scale (gLMS) which allows subjects to rate sensory intensity. Mothers were also evaluated for perception of the liquid formulation of the drug KaletrasupTM/sup, a recommended 1st line treatment for infants with HIV infection, whose taste is rejected by some children and accepted well by others. DNA samples from mothers were genotyped as a part of this study to identify (1) novel genes associated with human bitter perception and (2) the ability of compounds to block bitterness.

Link

study id = phs000839

Palabras clave

  1. 11/12/23 11/12/23 - Dr. Christian Niklas
Titular de derechos de autor

Julie A. Mennella, Monell Chemical Senses Center

Subido en

11 de diciembre de 2023

DOI

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Licencia

Creative Commons BY 4.0

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dbGaP phs000839 Bitter Blockers (BB)

Eligibility Criteria

Inclusion and exclusion criteria
Descripción

Inclusion and exclusion criteria

Alias
UMLS CUI [1,1]
C1512693
UMLS CUI [1,2]
C0680251
Women who were diabetic, pregnant, or lactating were not eligible; pregnancy tests were conducted on the day of testing to confirm non-pregnant status.
Descripción

Elig.phs000839.v1.p1.1

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0032961
UMLS CUI [1,2]
C2828358
UMLS CUI [1,3]
C0011849
UMLS CUI [1,4]
C1555471
UMLS CUI [1,5]
C0043210
UMLS CUI [2,1]
C0427777

Similar models

Eligibility Criteria

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
Inclusion and exclusion criteria
C1512693 (UMLS CUI [1,1])
C0680251 (UMLS CUI [1,2])
Elig.phs000839.v1.p1.1
Item
Women who were diabetic, pregnant, or lactating were not eligible; pregnancy tests were conducted on the day of testing to confirm non-pregnant status.
boolean
C0032961 (UMLS CUI [1,1])
C2828358 (UMLS CUI [1,2])
C0011849 (UMLS CUI [1,3])
C1555471 (UMLS CUI [1,4])
C0043210 (UMLS CUI [1,5])
C0427777 (UMLS CUI [2,1])

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