Evidence map›Paper›PMID 20484896›Full record

ArticleAmerican journal of nephrology2010

Progression of chronic kidney disease: Adrenergic genetic influence on glomerular filtration rate decline in hypertensive nephrosclerosis.

Yuqing Chen, Michael S Lipkowitz, Rany M Salem, Maple M Fung, Vibha Bhatnagar, Manjula Mahata, Caroline M Nievergelt, Fangwen Rao, Sushil K Mahata, Nicholas J Schork and 6 more

Open access · bronzeAbstract read
In one paragraph

Article in American journal of nephrology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 2 pooled it
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

10 citing papers in PubMed, 2 syntheses or guidelines pooled it, 14 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. βAmerican journal of physiology. Regulatory, integrative and comparative physiology · 2021
    Review
  4. Article
  5. Article
  6. Article
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  8. Article
  9. Sympathetic nerve traffic and asymmetric dimethylarginine in chronic kidney disease.Clinical journal of the American Society of Nephrology : CJASN · 2011
    Article
  10. 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

16 authors at 6 institutions in 4 countries.

Yuqing ChenRenal Division, Peking University First Hospital, Beijing, China.
Michael S Lipkowitz
Rany M Salem
Maple M Fung
Vibha Bhatnagar
Manjula Mahata
Caroline M Nievergelt
Fangwen Rao
Sushil K Mahata
Nicholas J Schork
Pamela J Hicks
Donald W Bowden
Barry I Freedman
Victoria H Brophy
Daniel T O'Connor
AASK
Wake Forest University · USGeneral Department of Preventive Medicine · VNIcahn School of Medicine at Mount Sinai · USPeking University First Hospital · CNRoche (Switzerland) · CHScripps Research Institute · US

Funding

ZOVIRAX CREAM TO TREAT HERPES LABIALIS IN ADOLESCENTSM01RR000827 · NCRR · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI CHANG, R JEFFREY · 1985 to 2010
$74.3M
Trafficking of catecholamine storage vesicle proteinsP01HL058120 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI ZIEGLER, MICHAEL G. · 1999 to 2009
$18.5M
San Diego EXPORT Comprehensive NCMHD Research CenterP60MD000220 · NIMHD · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI DALEY, SANDRA P · 2002 to 2011
$11.0M
NCRR NIH HHS M01 RR000827NCRR NIH HHS RR00827NHLBI NIH HHS P01 HL058120NIMHD NIH HHS MD000220NIMHD NIH HHS P60 MD000220
6 · The paper itself

Abstract

backgroundAfrican-Americans are likely to develop hypertension and hypertensive nephrosclerosis. This grave prognosis, coupled with familial aggregation of end-stage renal disease (ESRD) in Blacks, prompts a search for genetic risk factors for ESRD. Recent evidence implicates a crucial role for the sympathetic nervous system in progressive renal disease.

methodsWe used the African-American Study of Kidney Disease to probe whether beta2-adrenergic receptor (ADRB2) predicts glomerular filtration rate (GFR) decline rate. A total of 580 participants were included. Baseline GFR was 51.2 +/- 0.5 ml/min/1.73 m2. Subjects were randomized in a 2 x 3 block design: to intensively lowered (MAP < or = 92 mm Hg) versus 'usual' (MAP = 102-107 mm Hg) blood pressure goal groups, and also divided by three randomized antihypertensive drugs (ramipril, metoprolol, or amlodipine). We scored 4 SNPs at the ADRB2 locus.

resultsHaplotypes at ADRB2 predicted chronic GFR decline rate, GFR declined more slowly in individuals with haplotype-1 (-804G-->173T-->16Gly-->27GIn), and faster in those who carried haplotype-3 (-804G-->173T-->16Arg-->27Gln). ADRB2 genotype interacted with antihypertensive drug class to influence GFR slope (p = 0.001-0.037). We extended our findings to an independent case/control sample of Black hypertensive ESRD, in which we found that variant Gly16Arg that tagged the GFR slope-determining ADRB2 haplotype also conferred risk for the ESRD trait in Blacks.

conclusionsThe GFR decline/progression rate in hypertensive renal disease is controlled in part by genetic variation within the adrenergic pathway.

Indexed as

Hypertension, RenalNephrosclerosisRenal Insufficiency, ChronicAdultAgedAntihypertensive AgentsBlack or African AmericanDisease ProgressionDrug ResistanceFemaleGlomerular Filtration RateHumansMaleMiddle AgedMulticenter Studies as TopicRandomized Controlled Trials as TopicAntihypertensive AgentsReceptors, Adrenergic, beta-2

Identifiers

PMID20484896
PMCPMC2914391
OpenAlexW1970994800

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.