Evidence map›Paper›PMID 25002376›Full record

Trial reportThe Kaohsiung journal of medical sciences2014

Cyclosporine A combined with medium/low dose prednisone in progressive IgA nephropathy.

Lin Xu, Zhong-Cheng Liu, Guang-Ju Guan, Xue-Ai Lv, Qing Luo

Open access · goldAbstract readClinical Trial
In one paragraph

Trial report in The Kaohsiung journal of medical sciences, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 3 pooled it
1.1field-weighted citation impact, top 25% 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

13 citing papers in PubMed, 3 syntheses or guidelines pooled it, 17 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Trial
  5. Article
  6. Article
  7. Article
  8. Article
  9. Emerging Modes of Treatment of IgA Nephropathy.International journal of molecular sciences · 2020
    Review
  10. Review
  11. Article
  12. The Treatment of IgA Nephropathy.Kidney diseases (Basel, Switzerland) · 2015
    Review
  13. Identification of mannose-binding lectin as a mechanism in progressive immunoglobulin A nephropathy.International journal of clinical and experimental pathology · 2015
    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

5 authors at 3 institutions in 1 country.

Lin XuDepartment of Nephrology, The Second Hospital of Shandong University, Shandong University, Jinan, China; Department of Nephrology, Taian Central Hospital, Taian, China.
Zhong-Cheng LiuDepartment of Neurosurgery, The First People's Hospital of Taian, Taian, China.
Guang-Ju GuanDepartment of Nephrology, The Second Hospital of Shandong University, Shandong University, Jinan, China. Electronic address: guangj@sdu.edu.cn.
Xue-Ai LvDepartment of Nephrology, Taian Central Hospital, Taian, China.
Qing LuoBlood Purification Centre, Taian Central Hospital, Taian, China.
Second Hospital of Shandong University · CNTaian City Central Hospital · CNTaizhou First People's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The aim of the present study was to evaluate the efficacy of cyclosporine A (CsA) combined with medium/low dose prednisone in the treatment of progressive immunoglobulin A nephropathy (IgAN). Ninety-six patients who satisfied the inclusion criteria were enrolled in a prospective controlled clinical study. They were assigned into two groups and initially given either 0.6-0.8 mg/kg/day prednisone (maximum 40 mg/day) plus 3 mg/kg/day CsA (CsA group), or 1 mg/kg/day prednisone (maximum 60 mg/day) alone (steroid group). During therapy, the dose of prednisone was reduced in both groups and the dose of CsA was gradually tailed off over the first 3 months and maintained at 2 mg/kg/day in the CsA group. Urinary protein excretion, serum biochemical indexes, clinical efficacy and side effects of CsA were assayed. A significant decline in mean 24-hour urinary protein excretion (p < 0.05) was observed 1 month after treatment in patients in the CsA group, which was observed 2 months after treatment in the steroid group. The decline in mean 24-hour urinary protein excretion in the CsA group was more significant than in the steroid group. Serum albumin level increased significantly in the CsA group 2 months after therapy (p < 0.05). Moreover, at the end of the course, a higher remission rate was observed in patients with Lee's Grade III IgAN after combined treatment with prednisone and CsA (p < 0.05). No significant difference in clinical efficacy was observed in patients with Lee's Grade IV and Grade V IgAN between the two groups (p > 0.05). CsA at a dose of 2-3 mg/kg/day in combination with medium/low dose prednisone was effective in inducing remission of IgAN, especially for patients with Lee's Grade III IgAN, and is a safe and effective choice for short-term treatment of patients with progressive IgAN.

Indexed as

AdultBiomarkersCyclosporineDisease ProgressionDrug Therapy, CombinationFemaleGlomerulonephritis, IGAHumansMalePrednisoneTreatment OutcomeBiomarkersCyclosporinePrednisoneCyclosporine AIgA nephropathyPrednisone

Identifiers

PMID25002376
PMCPMC11916700
OpenAlexW2012346615

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.