Evidence map›Paper›PMID 28349446›Full record

ArticleInternational urology and nephrology2017

Hydroxychloroquine alleviates persistent proteinuria in IgA nephropathy.

Ruitong Gao, Wei Wu, Yubing Wen, Xuemei Li

Abstract read
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In one paragraph

Article in International urology and nephrology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed, 3 pooled it
4.0field-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

29 citing papers in PubMed, 3 syntheses or guidelines pooled it, 50 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Hydroxychloroquine use in pediatric IgA nephropathy.Pediatric nephrology (Berlin, Germany) · 2026
    Observational
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  18. Current treatment of IgA nephropathy.Seminars in immunopathology · 2021
    Review
  19. Article
  20. Mechanism of Action and Efficacy of Immunosupressors in Lupus Nephritis.International journal of nephrology and renovascular disease · 2021
    Review
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

4 authors at 2 institutions in 1 country.

Ruitong GaoDivision of Nephrology, Department of Internal Medicine, Peking Union Medical College Hospital, Beijing, 100730, People's Republic of China.
Wei WuDepartment of Clinical Laboratory, Peking Union Medical College Hospital, Beijing, 100730, People's Republic of China.
Yubing WenDivision of Nephrology, Department of Internal Medicine, Peking Union Medical College Hospital, Beijing, 100730, People's Republic of China.
Xuemei LiDivision of Nephrology, Department of Internal Medicine, Peking Union Medical College Hospital, Beijing, 100730, People's Republic of China. pumch_lixuemei@sina.com.
Chinese Academy of Medical Sciences & Peking Union Medical College · CNPeking Union Medical College Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeDendritic cells, Toll-like receptor (TLR), interleukin-6 (IFN-α), interferon-alpha (IFN-α) and tumor necrosis factor-alpha (TNF-α) play an important role in the pathogenesis of IgA nephropathy (IgAN). Hydroxychloroquine (HCQ) is an antimalarial agent and had a notable impact on immune activation by the reduction of circulating activated immune cells that including decreased TLR-expressing cells, reduced IFN-secreting DCs, reduced production of cytokines including IFN-α,IL-6 and TNF-α. We evaluated the efficacy of HCQ in reducing proteinuria in patients with IgAN.

methodsTwenty-eight IgAN patients with persistent proteinuria (0.5-2.0 g/24 h) despite treatment with losartan for 3 months were matched to receive HCQ and losartan (group 1) or continue losartan therapy (group 2) for 24 weeks. The primary end point of this prospective, paired case-control study was reduction of proteinuria by 50% or more over entry level.

resultsSix patients (42.9%) in group one versus two patients (14.3%) in group 2 reach the primary end point (P = 0.004). By 24 weeks, the mean urinary protein excretion was 65.9 ± 25.5% (P = 0.002) and 95.3 ± 30.0% (P = 0.791) that of the corresponding baseline value in group 1 and group 2, respectively. Baseline proteinuria and histologic grades, blood pressure control and changes in serum creatinine and eGFR were not different between the two groups.

conclusionsIn selected patients with IgAN, HCQ is effective in ameliorating proteinuria.

Indexed as

AdultAngiotensin II Type 1 Receptor BlockersAntimalarialsBlood PressureCase-Control StudiesCreatinineDrug Therapy, CombinationFemaleGlomerular Filtration RateGlomerulonephritis, IGAHumansHydroxychloroquineLosartanMaleMiddle AgedPilot ProjectsAngiotensin II Type 1 Receptor BlockersAntimalarialsCreatinineHydroxychloroquineLosartanHydroxychloroquineIgA nephropathyProteinuriaRemission

Identifiers

PMID28349446
OpenAlexW2598967641

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.