Evidence map›Paper›PMID 22116196›Full record

Trial reportKidney & blood pressure research2012

Clinical outcome of hyperuricemia in IgA nephropathy: a retrospective cohort study and randomized controlled trial.

Yongjun Shi, Wei Chen, Diana Jalal, Zhibin Li, Wenfang Chen, Haiping Mao, Qiongqiong Yang, Richard J Johnson, Xueqing Yu

Open access · bronzeAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Kidney & blood pressure research, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 80 papers, 16 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
80citing papers in PubMed, 16 pooled it
4.7field-weighted citation impact, top 5% 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

80 citing papers in PubMed, 16 syntheses or guidelines pooled it, 168 citations in OpenAlex.

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  4. Non-immunosuppressive treatment for IgA nephropathy.The Cochrane database of systematic reviews · 2024
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  7. Hyperuricemia aggravates the progression of IgA nephropathy.International urology and nephrology · 2022
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20 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

9 authors at 4 institutions in 2 countries.

Yongjun ShiDepartment of Nephrology, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Wei Chen
Diana Jalal
Zhibin Li
Wenfang Chen
Haiping Mao
Qiongqiong Yang
Richard J Johnson
Xueqing Yu
Pediatric Nephrology of Alabama · USUniversity of Colorado Denver · USSun Yat-sen University · CNThe First Affiliated Hospital, Sun Yat-sen University · CN

Funding

Role of Uric Acid in Hypertension and Renal DiseaseR01HL068607 · NHLBI · UNIVERSITY OF FLORIDA · PI JOHNSON, RICHARD JOSEPH · 2002 to 2011
$3.5M
GLOMERULAR ENDOTHELIAL CELL &HEMOLYTIC UREMIC SYNDROMER01DK052121 · NIDDK · UNIVERSITY OF WASHINGTON · PI JOHNSON, RICHARD JOSEPH · 1996 to 2009
$3.3M
Uric Acid as a Mediator of Endothelial Dysfunction in Patients with CKDK23DK088833 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI JALAL, DIANA I · 2010 to 2014
$897k
NHLBI NIH HHS HL-68607NHLBI NIH HHS R01 HL068607NIDDK NIH HHS DK-52121NIDDK NIH HHS K23 DK088833NIDDK NIH HHS R01 DK052121
6 · The paper itself

Abstract

backgroundHyperuricemia is an independent risk factor for renal progression in IgA nephropathy (IgAN). However, no study has evaluated the effect of allopurinol on the clinical outcome in hyperuricemic IgAN.

methodsFirst,a retrospective cohort study of 353 IgAN patients was conducted to explore the relationship between uric acid (UA) and the progression of renal disease over a mean period of 5 years. Then, 40 hyperuricemic IgAN patients were randomized to receive allopurinol (100-300 mg/day) or usual therapy for 6 months. The study outcomes were renal disease progression and/or blood pressure.

resultsHyperuricemia independently predicted renal survival at 1, 3, and 5 years after adjustment for different baseline estimated glomerular filtration rates. In the randomized controlled trial, allopurinol did not significantly alter renal progression or proteinuria. The antihypertensive drug dosage was reduced in 7 of 9 cases with hypertension in the allopurinol group compared to 0 of 9 cases in the control group (p < 0.01). UA levels correlated with mean arterial pressure in normotensive patients (r = 0.388, p < 0.001).

conclusionHyperuricemia predicts the progression of IgAN independently of baseline estimated glomerular filtration rate. Allopurinol may improve the control of blood pressure. Further studies are required to explore the effects of lowering UA on renal protection in IgAN.

Indexed as

AdolescentAdultAgedAllopurinolCohort StudiesFemaleFollow-Up StudiesGlomerulonephritis, IGAHumansHyperuricemiaMaleMiddle AgedPilot ProjectsProspective StudiesRetrospective StudiesTreatment OutcomeAllopurinol

Identifiers

PMID22116196
PMCPMC3242707
OpenAlexW2030058610

What Socratic 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 Socratic graph.