Evidence map›Paper›PMID 19965533›Full record

ArticleClinical journal of the American Society of Nephrology : CJASN2010

CRP polymorphisms and progression of chronic kidney disease in African Americans.

Adriana M Hung, Dana C Crawford, Marie R Griffin, Kristin Brown-Gentry, Michael S Lipkowitz, Edward D Siew, Kerri Cavanaugh, Julia B Lewis, T Alp Ikizler, AASK Study Group

Abstract read
In one paragraph

Article in Clinical journal of the American Society of Nephrology : CJASN, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.5field-weighted citation impact, top 16% 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

12 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
  2. C-reactive protein promotes diabetic kidney disease via Smad3-mediated NLRP3 inflammasome activation.Molecular therapy : the journal of the American Society of Gene Therapy · 2025
    Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. The pleiotropic effects of the hydroxy-methyl-glutaryl-CoA reductase inhibitors in renal disease.International journal of nephrology and renovascular disease · 2014
    Review
  9. Article
  10. Article
  11. Statins, inflammation and kidney disease.Nature reviews. Nephrology · 2011
    Review
  12. 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

10 authors at 4 institutions in 1 country.

Adriana M HungVanderbilt University Medical Center, 1161 21st Avenue South & Garland, Division of Nephrology, S-3223 MCN, Nashville, TN 37232-2372, USA. Adriana.hung@vanderbilt.edu
Dana C Crawford
Marie R Griffin
Kristin Brown-Gentry
Michael S Lipkowitz
Edward D Siew
Kerri Cavanaugh
Julia B Lewis
T Alp Ikizler
AASK Study Group
Center for Human Genetics · USIcahn School of Medicine at Mount Sinai · USVanderbilt University · USVA Tennessee Valley Healthcare System · US

Funding

VANDERBILT UNIVERSITY CTSA FOR PEDIATRIC RESEARCHUL1RR024975 · NCRR · VANDERBILT UNIVERSITY · PI BERNARD, GORDON RAPHAEL · 2007 to 2011
$45.7M
ZIPRASIDONE (GEODON) AUGMENTATION IN SEROTONIN REUPTAKE INHIBITOR-RESISTANT OBM01RR000071 · NCRR · MOUNT SINAI SCHOOL OF MEDICINE OF NYU · PI GOODMAN, MARC T · 1985 to 2009
$41.5M
Impact of Acute Kidney Injury on Kidney Disease ProgressionU01DK082192 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI IKIZLER, TALAT ALP · 2008 to 2018
$5.0M
GENES AND FIBRINOLYTIC CAPACITY OF HUMAN ENDOTHELIUMR01HL065193 · NHLBI · VANDERBILT UNIVERSITY · PI IKIZLER, TALAT ALP, PRETORIUS, MIAS · 2000 to 2012
$4.0M
AFRICAN AMERICAN STUDY OF KIDNEY DISEASE &HYPERTENSIONU01DK048689 · NIDDK · MOUNT SINAI SCHOOL OF MEDICINE OF NYU · PI LIPKOWITZ, MICHAEL · 1994 to 2007
$2.9M
ETIOLOGY OF NEPHROPATHY AND HYPERTENSION IN AASK PATIENTR01DK057867 · NIDDK · MOUNT SINAI SCHOOL OF MEDICINE OF NYU · PI LIPKOWITZ, MICHAEL S · 2000 to 2004
$1.9M
Nutrition and Metabolism in Dialysis PatientsK24DK062849 · NIDDK · VANDERBILT UNIVERSITY · PI IKIZLER, TALAT ALP · 2003 to 2012
$1.6M
Addressing Literacy and Numeracy in Self-care & Clinical Outcomes in ESRDK23DK080952 · NIDDK · VANDERBILT UNIVERSITY · PI CAVANAUGH, KERRI · 2008 to 2012
$915k
Omega-3 Fatty Acid Administration In Dialysis PatientsR21AT003844 · NCCIH · VANDERBILT UNIVERSITY · PI IKIZLER, TALAT ALP · 2008 to 2010
$596k
Inflammation, proteolysis and IL-1beta receptor inhibition in CHD patientsR21DK077373 · NIDDK · VANDERBILT UNIVERSITY · PI HUNG, ADRIANA · 2007 to 2008
$418k
NCCIH NIH HHS AT003844NCCIH NIH HHS R21 AT003844NCRR NIH HHS 1UL-1RR024975NCRR NIH HHS M01 RR000071NCRR NIH HHS RR000071NCRR NIH HHS UL1 RR024975NHLBI NIH HHS HL065193NHLBI NIH HHS R01 HL065193NIDDK NIH HHS DK048689NIDDK NIH HHS DK057867NIDDK NIH HHS DK077373NIDDK NIH HHS DK082192NIDDK NIH HHS DK62849NIDDK NIH HHS K23 DK080952NIDDK NIH HHS K23-DK080952-01NIDDK NIH HHS K24 DK062849NIDDK NIH HHS R01 DK057867NIDDK NIH HHS R21 DK077373NIDDK NIH HHS U01 DK048689NIDDK NIH HHS U01 DK082192
6 · The paper itself

Abstract

BACKGROUND AND

objectivesChronic inflammation may play a role in chronic kidney disease (CKD) progression. CRP gene polymorphisms are associated with serum C-reactive protein (CRP) concentrations. It is unknown if CRP polymorphisms are associated with CKD progression or modify the effectiveness of anti-hypertensive therapy in delaying CKD progression. DESIGN, SETTING, PARTICIPANTS, & MEASUREMENTS: We genotyped 642 participants with CKD from the African American Study of Kidney Disease and Hypertension (AASK), selecting five tag polymorphisms: rs2808630, rs1205, rs3093066, rs1417938, and rs3093058. We compared the minor allele frequencies (MAF) of single nucleotide polymorphisms (SNPs) in AASK to MAFs of African Americans from NHANES III. Among AASK participants, we evaluated the association of SNPs with CRP levels and prospectively with a composite: halving the GFR, ESRD, or death.

resultsThe MAF was higher for the rs2808630_G allele (P = 0.03) and lower for the rs1205_A allele (P = 0.03) in the AASK compared with NHANES III. Among AASK participants, the rs3093058_T allele predicted higher CRP concentrations (P < 0.0001) but not CKD progression. The rs2808630_GG genotype was associated with higher risk of the composite endpoint compared with the AA genotype (P = 0.002). Participants with the rs2808630_GG genotype on angiotensin converting enzyme inhibitors (ACEIs) versus beta blockers had increased risk of progression (P = 0.03).

conclusionCRP SNPs that were associated with higher levels of CRP did not predict CKD progression. The rs2808630_GG genotype was associated with higher risk of CKD progression, and in patients with this genotype, ACEIs did not slow progression.

Indexed as

Black or African AmericanPolymorphism, GeneticAngiotensin-Converting Enzyme InhibitorsChronic DiseaseC-Reactive ProteinDisease ProgressionFemaleHumansKidney DiseasesMaleMiddle AgedProspective StudiesAngiotensin-Converting Enzyme InhibitorsC-Reactive Protein

Identifiers

PMID19965533
PMCPMC2801650
OpenAlexW2141901627

What OpenQuestion holds

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Registered trials

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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.