Evidence map›Paper›PMID 30876802›Full record

ArticleThe Journal of investigative dermatology2019

Demographics and Autoantibody Profiles of Pemphigoid Patients with Underlying Neurologic Diseases.

Kelly N Messingham, Adam D Miller, Nandakumar S Narayanan, Samuel J Connell, Janet A Fairley

Open access · greenAbstract read
In one paragraph

Article in The Journal of investigative dermatology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

7 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
  2. Peptide Epitopes of NC16A BP180 in the Diagnostics of Bullous Pemphigoid.JID innovations : skin science from molecules to population health · 2025
    Article
  3. Article
  4. Article
  5. The Relationship Between Alzheimer's Disease and Skin Diseases: A Review.Clinical, cosmetic and investigational dermatology · 2021
    Review
  6. Article
  7. The pathogenesis of bullous skin diseases.Journal of translational autoimmunity · 2019
    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

5 authors at 1 institution in 1 country.

Kelly N MessinghamDepartment of Dermatology, University of Iowa, Iowa City, Iowa, USA.
Adam D MillerDepartment of Dermatology, University of Iowa, Iowa City, Iowa, USA.
Nandakumar S NarayananDepartment of Neurology, University of Iowa, Iowa City, Iowa, USA.
Samuel J ConnellDepartment of Dermatology, University of Iowa, Iowa City, Iowa, USA.
Janet A FairleyDepartment of Dermatology, University of Iowa, Iowa City, Iowa, USA; Iowa City Veterans Affairs Medical Center, Iowa City, Iowa, USA. Electronic address: janet-fairley@uiowa.edu.
University of Iowa · US

Funding

The University of Iowa Clinical and Translational Science AwardUL1TR002537 · NCATS · UNIVERSITY OF IOWA · PI HANSEN, MARLAN R, WINOKUR, PATRICIA · 2018 to 2022
$20.0M
The University of Iowa Clinical and Translational Science AwardU54TR001356 · NCATS · UNIVERSITY OF IOWA · PI WINOKUR, PATRICIA · 2015 to 2016
$7.1M
SHORT-TERM TRAINING: STUDENTS IN HEALTH PROF. SCHOOLST35HL007485 · NHLBI · UNIVERSITY OF IOWA · PI ROGHAIR, ROBERT D · 1985 to 2019
$4.3M
The Role of IgE in Autoimmune Skin DiseasesI01CX000317 · VA · IOWA CITY VA MEDICAL CENTER · PI FAIRLEY, JANET A · 2011 to 2013
–
CSRD VA I01 CX000317NCATS NIH HHS U54 TR001356NCATS NIH HHS UL1 TR002537NHLBI NIH HHS T35 HL007485
6 · The paper itself

Abstract

Bullous pemphigoid (BP) is an autoantibody-mediated blistering disease that is often associated with neurologic disease. BP antibodies target two epidermal adhesion molecules, known as BP180 and BP230. Homologues to these proteins are found in the brain, and it is hypothesized that neurologic disease leads to the production of autoantibodies that can cross-react with their cutaneous forms. To better understand the link between BP and neurologic disease, we evaluated primary demographic features (age, sex, race, ethnicity, and elapsed time between onset of skin symptoms and BP diagnosis), severity of BP, and IgG and IgE autoantibody levels in BP control individuals and patients with BP with preceding Parkinson disease, dementia, and stroke. The main findings of this study are that patients with BP with preceding neurologic disease have a shorter elapsed time between onset of skin disease and BP diagnosis and that patients with preceding Parkinson disease or dementia, but not stroke, are significantly older than patients with BP without neurologic disease. However, no significant differences in clinical presentation, BP severity scores, or autoantibody (IgG and IgE) responses were observed among the groups. These findings suggest that, despite the age difference, the clinical phenotype of BP is not affected by preceding neurologic disease.

Indexed as

AgedAged, 80 and overAge FactorsAge of OnsetAutoantibodiesAutoantigensCollagen Type XVIIComorbidityDementiaDystoninFemaleHumansIncidenceMaleMiddle AgedNon-Fibrillar CollagensAutoantibodiesAutoantigensCollagen Type XVIIDST protein, humanDystoninNon-Fibrillar Collagens

Identifiers

PMID30876802
PMCPMC6910721
OpenAlexW2920882116

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.