Evidence map›Paper›PMID 21193038›Full record

ArticleThe Journal of steroid biochemistry and molecular biology2011

Associations between polymorphisms in glucuronidation and sulfation enzymes and sex steroid concentrations in premenopausal women in the United States.

Mellissa Yong, Stephen M Schwartz, Charlotte Atkinson, Karen W Makar, Sushma S Thomas, Frank Z Stanczyk, Kim C Westerlind, Katherine M Newton, Victoria L Holt, Wendy M Leisenring and 1 more

Open access · greenAbstract read
In one paragraph

Article in The Journal of steroid biochemistry and molecular biology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
3.4field-weighted citation impact, top 9% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

11 citing papers in PubMed, 21 citations in OpenAlex.

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  11. Functional polymorphisms in UDP-glucuronosyl transferases and recurrence in tamoxifen-treated breast cancer survivors.Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology · 2011
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors at 5 institutions in 2 countries.

Mellissa YongFred Hutchinson Cancer Research Center, Seattle, WA 98109, USA.
Stephen M Schwartz
Charlotte Atkinson
Karen W Makar
Sushma S Thomas
Frank Z Stanczyk
Kim C Westerlind
Katherine M Newton
Victoria L Holt
Wendy M Leisenring
Johanna W Lampe
Fred Hutch Cancer Center · USCancer Research Center · USKaiser Permanente Washington Health Research Institute · USUniversity of Bristol · GBUniversity of Southern California · US

Funding

Breast and Bone Density: Impact of Colonic EnvironmentR01CA097366 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI LAMPE, JOHANNA W · 2003 to 2006
$1.9M
UGT Polymorphisms and Hormonally-Mediated Biomarkers in Premenopausal WomenR03CA121872 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI LAMPE, JOHANNA W · 2007 to 2008
$158k
NCI NIH HHS R01 CA097366NCI NIH HHS R01CA097366NCI NIH HHS R03 CA121872NCI NIH HHS R03CA121872
6 · The paper itself

Abstract

Glucuronidation, catalyzed by UDP-glucuronosyltransferases (UGT) and sulfation, catalyzed by sulfotransferases (SULT), are pathways through which sex steroids are metabolized to less active compounds. These enzymes are highly polymorphic and genetic variants frequently result in higher or lower activity. The phenotypic effects of these polymorphisms on circulating sex steroids in premenopausal women have not yet been investigated. One hundred and seventy women aged 40-45 years had a blood sample drawn during the follicular phase of the menstrual cycle for sex steroid measures and to obtain genomic DNA. Urine was collected for 2-hydroxy (OH) estrone (E(1)) and 16α-OH E(1) measures. Generalized linear regression models were used to assess associations between sex steroids and polymorphisms in the UGT1A and UGT2B families, SULT1A1, and SULT1E1. Women with the UGT1A1(TA7/TA7) genotype had 25% lower mean estradiol (E(2)) concentrations compared to the wildtype (TA6/TA6) (p=0.02). Similar associations were observed between SULT1A1(R213/H213) and E(1) (13% lower mean E(1) concentration vs. wildtype; p-value=0.02) and UGT2B4(E458/E458) and dehydroepiandrosterone (DHEA) (20% lower mean DHEA vs. wildtype; p-value=0.03). The SULT1E1(A/C) and the UGT1A1(TA7)-UGT1A3(R11) haplotypes were associated with reduced estrogen concentrations. Further study of UGT and SULT polymorphisms and circulating sex steroid measures in larger populations of premenopausal women is warranted.

Indexed as

AdultDehydroepiandrosteroneDNAEstradiolEstroneFemaleGenetic VariationGlucuronosyltransferaseHaplotypesHumansLinear ModelsMiddle AgedPolymerase Chain ReactionPolymorphism, GeneticPremenopauseSulfotransferasesDehydroepiandrosteroneDNAEstradiolEstroneGlucuronosyltransferaseSulfotransferases

Identifiers

PMID21193038
PMCPMC3065887
OpenAlexW2024687930

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.