Evidence map›Paper›PMID 16897191›Full record

ArticleJournal of human genetics2006

Polymorphisms in interleukin 8 and its receptors (IL8, IL8RA and IL8RB) and association of common IL8 receptor variants with peripheral blood eosinophil counts.

Hyun Sub Cheong, Hyoung Doo Shin, Soo Ok Lee, Byung Lae Park, Yoo Hyun Choi, Gun Il Lim, Soo Taek Uh, Young Hun Kim, Jong-Young Lee, Jong-Keuk Lee and 8 more

Open access · bronzeAbstract read
PubMed Publisher
In one paragraph

Article in Journal of human genetics, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.7field-weighted citation impact, top 30% 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

4 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. 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

18 authors at 6 institutions in 1 country.

Hyun Sub CheongDepartment of Genetic Epidemiology, SNP Genetics, Inc., Rm 1407, 14th floor, B-dong, WooLim Lion's Valley, 371-28, Gasan-dong, Geumcheon-Gu, Seoul, 153-803, South Korea.
Hyoung Doo ShinDepartment of Genetic Epidemiology, SNP Genetics, Inc., Rm 1407, 14th floor, B-dong, WooLim Lion's Valley, 371-28, Gasan-dong, Geumcheon-Gu, Seoul, 153-803, South Korea.
Soo Ok LeeDepartment of Genetic Epidemiology, SNP Genetics, Inc., Rm 1407, 14th floor, B-dong, WooLim Lion's Valley, 371-28, Gasan-dong, Geumcheon-Gu, Seoul, 153-803, South Korea.
Byung Lae ParkDepartment of Genetic Epidemiology, SNP Genetics, Inc., Rm 1407, 14th floor, B-dong, WooLim Lion's Valley, 371-28, Gasan-dong, Geumcheon-Gu, Seoul, 153-803, South Korea.
Yoo Hyun ChoiDepartment of Genetic Epidemiology, SNP Genetics, Inc., Rm 1407, 14th floor, B-dong, WooLim Lion's Valley, 371-28, Gasan-dong, Geumcheon-Gu, Seoul, 153-803, South Korea.
Gun Il LimAsthma Genome Research Group, Soonchunhyang University Hospital, Seoul, South Korea.
Soo Taek UhAsthma Genome Research Group, Ajuo University Hospital, Seoul, South Korea.
Young Hun KimAsthma Genome Research Group, Ulsan University Hospital, Seoul, South Korea.
Jong-Young LeeAsthma Genome Research Group, Choong-Ang University, Seoul, South Korea.
Jong-Keuk LeeNational Genome Research Institute, National Institute of Health, 5 Nokbun-dong, Eunpyung-ku, Seoul, 122-701, South Korea.
Hung Tae KimNational Genome Research Institute, National Institute of Health, 5 Nokbun-dong, Eunpyung-ku, Seoul, 122-701, South Korea.
Ha-Jung RyuNational Genome Research Institute, National Institute of Health, 5 Nokbun-dong, Eunpyung-ku, Seoul, 122-701, South Korea.
Ka-Kyung KimNational Genome Research Institute, National Institute of Health, 5 Nokbun-dong, Eunpyung-ku, Seoul, 122-701, South Korea.
Bok Ghee HanNational Genome Research Institute, National Institute of Health, 5 Nokbun-dong, Eunpyung-ku, Seoul, 122-701, South Korea.
Jun Woo KimNational Genome Research Institute, National Institute of Health, 5 Nokbun-dong, Eunpyung-ku, Seoul, 122-701, South Korea.
Kuchan KimmNational Genome Research Institute, National Institute of Health, 5 Nokbun-dong, Eunpyung-ku, Seoul, 122-701, South Korea.
Bermseok OhNational Genome Research Institute, National Institute of Health, 5 Nokbun-dong, Eunpyung-ku, Seoul, 122-701, South Korea. ohbs@nih.go.kr.
Choon-Sik ParkAsthma Genome Research Group, Soonchunhyang University Hospital, Seoul, South Korea. schalr@schbc.ac.kr.
Korea National Institute of Health · KRSNP Genetics (South Korea) · KRBucheon University · KRChung-Ang University · KRSoonchunhyang University Hospital · KRUlsan University Hospital · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Airway inflammation is a major factor in the pathogenesis of asthma. Interleukin 8 (IL8) is a potent proinflammatory cytokine that interacts with its receptors, IL8RA and IL8RB. We investigated the genetic polymorphisms in IL8, IL8RA, and IL8RB for any association with risk of asthma and peripheral blood eosinophil counts in a Korean population. By carrying out direct sequencing in 24 individuals, we identified 20 sequence variants within exons and their flanking regions, including the 1.5 kb promoter regions of IL8, IL8RA, and IL8RB. Among them, seven common single-nucleotide polymorphisms (SNPs) were selected for genotyping in our asthma cohort (n = 1,439). Two common haplotypes in IL8 and three in IL8RA and IL8RB (defined as one block) were identified. Although none of the polymorphisms showed a significant association with risk of asthma, IL8RA-B ht2 showed a significant association with the peripheral blood eosinophil counts (%) among asthma patients, e.g., lower eosinophil levels among individuals with the homozygous IL8RA-B ht2 (3.55 +/- 3.39%) than among other asthmatic patients (5.52 +/- 5.55%; P (corr) = 0.018). Our findings suggest that polymorphisms and haplotypes in IL8RA and IL8RB might be among the genetic factors underlying production of peripheral blood eosinophil.

Indexed as

AdolescentAdultAgedAged, 80 and overAsthmaCase-Control StudiesChildChild, PreschoolEosinophilsFemaleGenetic VariationHumansInterleukin-8KoreaLeukocyte CountMaleInterleukin-8Receptors, Interleukin-8AReceptors, Interleukin-8B

Identifiers

PMID16897191
OpenAlexW2035868549

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.