Evidence map›Paper›PMID 28509128›Full record

ArticleCEN case reports2017

A case of rapid amelioration of hepatitis C virus-associated cryoglobulinemic membranoproliferative glomerulonephritis treated by interferon-free directly acting antivirals for HCV in the absence of immunosuppressant.

Fumiaki Obata, Taichi Murakami, Junko Miyagi, Sayo Ueda, Taizo Inagaki, Masanori Minato, Hiroyuki Ono, Kenji Nishimura, Eriko Shibata, Masanori Tamaki and 7 more

Open access · greenAbstract read
In one paragraph

Article in CEN case reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.4field-weighted citation impact, top 17% 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

9 citing papers in PubMed, 13 citations in OpenAlex.

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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

17 authors at 2 institutions in 1 country.

Fumiaki ObataDepartment of Nephrology, Tokushima University Graduate School of Biomedical Science, 3-18-15 Kuramoto-cho, Tokushima, Tokushima, 770-8503, Japan.
Taichi MurakamiDepartment of Nephrology, Tokushima University Graduate School of Biomedical Science, 3-18-15 Kuramoto-cho, Tokushima, Tokushima, 770-8503, Japan. murakami.taichi@tokushima-u.ac.jp.
Junko MiyagiDepartment of Internal Medicine, Local Incorporated Administrative Agency Tokushima Prefecture Naruto Hospital, 32 Kurozaki-aza-kotani, Muya-cho, Naruto, Tokushima, 772-8503, Japan.
Sayo UedaDepartment of Nephrology, Tokushima University Graduate School of Biomedical Science, 3-18-15 Kuramoto-cho, Tokushima, Tokushima, 770-8503, Japan.
Taizo InagakiDepartment of Nephrology, Tokushima University Graduate School of Biomedical Science, 3-18-15 Kuramoto-cho, Tokushima, Tokushima, 770-8503, Japan.
Masanori MinatoDepartment of Nephrology, Tokushima University Graduate School of Biomedical Science, 3-18-15 Kuramoto-cho, Tokushima, Tokushima, 770-8503, Japan.
Hiroyuki OnoDepartment of Nephrology, Tokushima University Graduate School of Biomedical Science, 3-18-15 Kuramoto-cho, Tokushima, Tokushima, 770-8503, Japan.
Kenji NishimuraDepartment of Nephrology, Tokushima University Graduate School of Biomedical Science, 3-18-15 Kuramoto-cho, Tokushima, Tokushima, 770-8503, Japan.
Eriko ShibataDepartment of Nephrology, Tokushima University Graduate School of Biomedical Science, 3-18-15 Kuramoto-cho, Tokushima, Tokushima, 770-8503, Japan.
Masanori TamakiDepartment of Nephrology, Tokushima University Graduate School of Biomedical Science, 3-18-15 Kuramoto-cho, Tokushima, Tokushima, 770-8503, Japan.
Sakiya YoshimotoDepartment of Nephrology, Tokushima University Graduate School of Biomedical Science, 3-18-15 Kuramoto-cho, Tokushima, Tokushima, 770-8503, Japan.
Fumi KishiDepartment of Nephrology, Tokushima University Graduate School of Biomedical Science, 3-18-15 Kuramoto-cho, Tokushima, Tokushima, 770-8503, Japan.
Seiji KishiDepartment of Nephrology, Tokushima University Graduate School of Biomedical Science, 3-18-15 Kuramoto-cho, Tokushima, Tokushima, 770-8503, Japan.
Motokazu MatsuuraDepartment of Nephrology, Tokushima University Graduate School of Biomedical Science, 3-18-15 Kuramoto-cho, Tokushima, Tokushima, 770-8503, Japan.
Kojiro NagaiDepartment of Nephrology, Tokushima University Graduate School of Biomedical Science, 3-18-15 Kuramoto-cho, Tokushima, Tokushima, 770-8503, Japan.
Hideharu AbeDepartment of Nephrology, Tokushima University Graduate School of Biomedical Science, 3-18-15 Kuramoto-cho, Tokushima, Tokushima, 770-8503, Japan.
Toshio DoiDepartment of Nephrology, Tokushima University Graduate School of Biomedical Science, 3-18-15 Kuramoto-cho, Tokushima, Tokushima, 770-8503, Japan.
Tokushima University · JPNaruto, Tokushima Prefecture hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mixed cryoglobulinemic syndrome, which is a systemic vasculitis characterized by the immune complex deposition in small- and medium-sized arteries and most often due to chronic hepatitis C virus (HCV) infection, sometimes clinically manifests as refractory glomerulonephritis or nephritic syndrome. Patients with mixed cryoglobulinemic nephropathy who have a rapidly progressive glomerulonephritis should receive immunosuppressive therapy. After disease stabilization, patients should receive concurrent therapy for the underlying HCV infection. The standard therapy of a chronic HCV infection is IFN monotherapy or IFN combined with ribavirin; however, after the introduction of direct-acting antivirals (DAAs), the standard therapy for patients with HCV genotype 1 has dramatically changed. We report a case of HCV-associated cryoglobulinemic membranoproliferative glomerulonephritis (MPGN) successfully treated by daclatasvir and asunaprevir, which are IFN-free DAAs for HCV, in combination with angiotensin II receptor blocker without immunosuppressive therapy. The patient developed severe nephrotic syndrome with progressive kidney dysfunction. Blood examination revealed a high copy number of HCV-RNA (6.4 log IU/mL, type 1), cryoglobulinemia, paraproteinemia of IgM-κ, and hypocomplementemia. Histological analysis showed MPGN type 1. These findings were compatible with those observed in HCV-associated cryoglobulinemic MPGN. This case offers original evidence for the application of newer generation of IFN-free DAAs in the treatment of HCV-associated cryoglobulinemic nephropathy.

Indexed as

Cryoglobulinemic membranoproliferative glomerulonephritisHepatitis C virusInterferon-free direct-acting antiviral agents

Identifiers

PMID28509128
PMCPMC5438808
OpenAlexW2555787358

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.