Evidence map›Paper›PMID 26762549›Full record

ReviewAmerican journal of medical genetics. Part A2016

Auricular ossification: A newly recognized feature of osteoprotegerin-deficiency juvenile Paget disease.

Gary S Gottesman, Katherine L Madson, William H McAlister, Angela Nenninger, Deborah Wenkert, Steven Mumm, Michael P Whyte

Abstract readCase ReportsReview
In one paragraph

Review in American journal of medical genetics. Part A, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.3field-weighted citation impact, top 19% 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

4 citing papers in PubMed, 15 citations in OpenAlex.

  1. Review
  2. Article
  3. Genetic disorders associated with the RANKL/OPG/RANK pathway.Journal of bone and mineral metabolism · 2021
    Review
  4. 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

7 authors at 3 institutions in 1 country.

Gary S GottesmanCenter for Metabolic Bone Disease and Molecular Research, Shriners Hospital for Children, St. Louis, Missouri.
Katherine L MadsonCenter for Metabolic Bone Disease and Molecular Research, Shriners Hospital for Children, St. Louis, Missouri.
William H McAlisterMallinckrodt Institute of Radiology, Washington University School of Medicine at St. Louis Children's Hospital, St. Louis, Missouri.
Angela NenningerCenter for Metabolic Bone Disease and Molecular Research, Shriners Hospital for Children, St. Louis, Missouri.
Deborah WenkertCenter for Metabolic Bone Disease and Molecular Research, Shriners Hospital for Children, St. Louis, Missouri.
Steven MummCenter for Metabolic Bone Disease and Molecular Research, Shriners Hospital for Children, St. Louis, Missouri.
Michael P WhyteCenter for Metabolic Bone Disease and Molecular Research, Shriners Hospital for Children, St. Louis, Missouri.
Shriners Hospitals for Children - Erie · USBarnes-Jewish Hospital · USSt. Louis Children's Hospital · US

Funding

GENETIC BASES FOR DISEASES OF THE RANK SIGNALING PATHWAYR01DK067145 · NIDDK · WASHINGTON UNIVERSITY · PI MUMM, STEVEN R · 2010 to 2013
$1.3M
NIDDK NIH HHS DK067145NIDDK NIH HHS R01 DK067145
6 · The paper itself

Abstract

We report auricular ossification (AO) affecting the elastic cartilage of the ear as a newly recognized feature of osteoprotegerin (OPG)-deficiency juvenile Paget disease (JPD). AO and auricular calcification refer interchangeably to rigid pinnae, sparing the ear lobe, from various etiologies. JPD is a rare Mendelian disorder characterized by elevated serum alkaline phosphatase activity accompanied by skeletal pain and deformity from rapid bone turnover. Autosomal recessive transmission of loss-of-function mutations within TNFRSF11B encoding OPG accounts for most JPD (JPD1). JPD2 results from heterozygous constitutive activation of TNFRSF11A encoding RANK. Other causes of JPD remain unknown. In 2007, we reported a 60-year-old man with JPD1 who described hardening of his external ears at age 45 years, after 4 years of treatment with bisphosphonates (BPs). Subsequently, we noted rigid pinnae in a 17-year-old boy and 14-year-old girl, yet pliable pinnae in a 12-year-old boy, each with JPD1 and several years of BP treatment. Cranial imaging indicated cortical bone within the pinnae of both teenagers. Radiologic studies of our three JPD patients without mutations in TNFRSF11B showed normal auricles. Review of the JPD literature revealed possible AO in several reports. Two of our JPD1 patients had experienced difficult tracheal intubation, raising concern for mineralization of laryngeal elastic cartilage. Thus, AO is a newly recognized feature of JPD1, possibly exacerbated by BP treatment. Elastic cartilage at other sites in JPD1 might also ossify, and warrants investigation.

Indexed as

Genetic Association StudiesAdolescentAgedBone and BonesDNA Mutational AnalysisEar AuricleFemaleHumansMaleMutationOssification, HeterotopicOsteitis DeformansOsteoprotegerinPhenotypeTomography, X-Ray ComputedYoung AdultOsteoprotegerinantiresorptivesbisphosphonatesectopic calcificationelastic cartilagevascular calcification

Identifiers

PMID26762549
PMCPMC5111855
OpenAlexW2237334409

What OpenQuestion holds

Textmetadata
LicenceTDM
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.