Evidence map›Paper›PMID 21357676›Full record

SynthesisHuman molecular genetics2011

Sequence variants at CYP1A1-CYP1A2 and AHR associate with coffee consumption.

Patrick Sulem, Daniel F Gudbjartsson, Frank Geller, Inga Prokopenko, Bjarke Feenstra, Katja K H Aben, Barbara Franke, Martin den Heijer, Peter Kovacs, Michael Stumvoll and 20 more

Open access · bronzeAbstract readMeta-Analysis
In one paragraph

Synthesis in Human molecular genetics, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 70 papers, 10 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
70citing papers in PubMed, 10 pooled it
10.3field-weighted citation impact, top 1% 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

70 citing papers in PubMed, 10 syntheses or guidelines pooled it, 149 citations in OpenAlex.

  1. Pooled it
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  5. Journal of the American Society of Nephrology : JASN · 2017
    Pooled it
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  7. Genetic comorbidities in Parkinson's disease.Human molecular genetics · 2014
    Pooled it
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  11. Trial
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  19. Review
  20. Coffee: Fuel for Your Day or Foe for Your Arteries.Antioxidants (Basel, Switzerland) · 2024
    Review

10 more citing papers are in PubMed but not listed here.

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

30 authors at 9 institutions in 6 countries.

Patrick SulemdeCODE Genetics, Sturlugata 8, 101 Reykjavik, Iceland. patrick.sulem@decode.is
Daniel F Gudbjartsson
Frank Geller
Inga Prokopenko
Bjarke Feenstra
Katja K H Aben
Barbara Franke
Martin den Heijer
Peter Kovacs
Michael Stumvoll
Reedik Mägi
Lisa R Yanek
Lewis C Becker
Heather A Boyd
Simon N Stacey
G Bragi Walters
Adalbjorg Jonasdottir
Gudmar Thorleifsson
Hilma Holm
Sigurjon A Gudjonsson
Thorunn Rafnar
Gyda Björnsdottir
Diane M Becker
Mads Melbye
Augustine Kong
Anke Tönjes
Thorgeir Thorgeirsson
Unnur Thorsteinsdottir
Lambertus A Kiemeney
Kari Stefansson
deCODE Genetics (Iceland) · ISStatens Serum Institut · DKCentre for Human Genetics · GBJohns Hopkins University · USRadboud University Nijmegen · NLCenter for Clinical Research (United States) · USEast Harlem Tutorial Program · USLeipzig University · DELeipzig University of Applied Sciences · DE

Funding

Genes contributing to nicotine dependence in humansR01DA017932 · NIDA · DECODE GENETICS, INC. · PI STEFANSSON, KARI · 2005 to 2015
$9.6M
NIDA NIH HHS R01 DA017932NIDA NIH HHS R01-DA017932
6 · The paper itself

Abstract

Coffee is the most commonly used stimulant and caffeine is its main psychoactive ingredient. The heritability of coffee consumption has been estimated at around 50%. We performed a meta-analysis of four genome-wide association studies of coffee consumption among coffee drinkers from Iceland (n = 2680), The Netherlands (n = 2791), the Sorbs Slavonic population isolate in Germany (n = 771) and the USA (n = 369) using both directly genotyped and imputed single nucleotide polymorphisms (SNPs) (2.5 million SNPs). SNPs at the two most significant loci were also genotyped in a sample set from Iceland (n = 2430) and a Danish sample set consisting of pregnant women (n = 1620). Combining all data, two sequence variants significantly associated with increased coffee consumption: rs2472297-T located between CYP1A1 and CYP1A2 at 15q24 (P = 5.4 · 10(-14)) and rs6968865-T near aryl hydrocarbon receptor (AHR) at 7p21 (P = 2.3 · 10(-11)). An effect of ∼0.2 cups a day per allele was observed for both SNPs. CYP1A2 is the main caffeine metabolizing enzyme and is also involved in drug metabolism. AHR detects xenobiotics, such as polycyclic aryl hydrocarbons found in roasted coffee, and induces transcription of CYP1A1 and CYP1A2. The association of these SNPs with coffee consumption was present in both smokers and non-smokers.

Indexed as

Genetic VariationAdultAgedAllelesChromosomes, Human, Pair 15CoffeeCytochrome P-450 CYP1A1Cytochrome P-450 CYP1A2Drinking BehaviorFemaleGenome-Wide Association StudyHumansMaleMiddle AgedModels, BiologicalPolymorphism, Single NucleotideCoffeeCytochrome P-450 CYP1A1Cytochrome P-450 CYP1A2Receptors, Aryl Hydrocarbon

Identifiers

PMID21357676
PMCPMC3080612
OpenAlexW2102325625

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.