Evidence map›Paper›PMID 25194005›Full record

ArticleJournal of the American Society of Nephrology : JASN2015

IgD heavy-chain deposition disease: detection by laser microdissection and mass spectrometry.

Virginie Royal, Patrick Quint, Martine Leblanc, Richard LeBlanc, Garrett F Duncanson, Robert L Perrizo, Fernando C Fervenza, Paul Kurtin, Sanjeev Sethi

Open access · bronzeAbstract readCase Reports
In one paragraph

Article in Journal of the American Society of Nephrology : JASN, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
1.6field-weighted citation impact, top 18% 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, 1 synthesis or guideline pooled it, 37 citations in OpenAlex.

  1. Guideline
  2. Article
  3. Review
  4. Article
  5. Review
  6. Review
  7. Article
  8. [Advances in diagnosis and treatment of monoclonal immunoglobulin deposit disease].Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi · 2020
    Article
  9. Article
  10. The Complexity and Heterogeneity of Monoclonal Immunoglobulin-Associated Renal Diseases.Journal of the American Society of Nephrology : JASN · 2018
    Review
  11. Review
  12. Article
  13. 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

9 authors at 4 institutions in 3 countries.

Virginie RoyalDepartments of Pathology and Cytology.
Patrick QuintDepartment of Laboratory Medicine and Pathology and.
Martine LeblancNephrology, and.
Richard LeBlancHematology-Oncology, Maisonneuve-Rosemont Hospital, Montreal, Canada; and.
Garrett F DuncansonDepartment of Laboratory Medicine and Pathology and.
Robert L PerrizoDepartment of Laboratory Medicine and Pathology and.
Fernando C FervenzaDivision of Nephrology and Hypertension, Mayo Clinic, Rochester, Minnesota.
Paul KurtinDepartment of Laboratory Medicine and Pathology and.
Sanjeev SethiDepartment of Laboratory Medicine and Pathology and sethi.sanjeev@mayo.edu.
Mayo Clinic · USHôpital Maisonneuve-Rosemont · CAInstitute of Cytology · RUPediatric Nephrology of Alabama · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Monoclonal Ig deposition disease (MIDD) is a rare complication of monoclonal gammopathy characterized by deposition of monoclonal Ig light chains and/or heavy chains along the glomerular and tubular basement membranes. Here, we describe a unique case of IgD deposition disease. IgD deposition is difficult to diagnose, because routine immunofluorescence does not detect IgD. A 77-year-old man presented with proteinuria and renal failure, and kidney biopsy analysis showed a nodular sclerosing GN with extensive focal global glomerulosclerosis, tubular atrophy, and interstitial fibrosis. Immunofluorescence was negative for Ig deposits, although electron microscopy showed deposits in the glomeruli and along tubular basement membranes. Laser microdissection of glomeruli and mass spectrometry of extracted peptides showed a large spectra number for IgD, and immunohistochemistry showed intense glomerular and tubular staining for IgD. Together, these findings are consistent with IgD deposition disease. Bone marrow biopsy analysis showed 5% plasma cells, which stained for IgD. The patient was treated with bortezomib and dexamethasone, which resulted in improvement of hematologic parameters but no improvement of renal function. The diagnosis of IgD deposition disease underscores the value of laser microdissection and mass spectrometry in further evaluating renal biopsies when routine assessment fails to reach an accurate diagnosis.

Indexed as

AgedBiopsyHeavy Chain DiseaseHumansImmunoglobulin delta-ChainsKidneyKidney DiseasesLaser Capture MicrodissectionMaleMass SpectrometryImmunoglobulin delta-Chainsimmunology and pathologymultiple myelomarenal pathology

Identifiers

PMID25194005
PMCPMC4378111
OpenAlexW2142701069

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.