Evidence map›Paper›PMID 30634988›Full record

ArticleOrphanet journal of rare diseases2019

Infection risk among adults with down syndrome: a two group series of 101 patients in a tertiary center.

Aurélien Guffroy, Yannick Dieudonné, Beatrice Uring-Lambert, Joelle Goetz, Yves Alembik, Anne-Sophie Korganow

Registry-linked trialOpen access · goldAbstract readLetter
In one paragraph

Article in Orphanet journal of rare diseases, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01663675 (Trisomy 21 in Adulthood. Evaluation of Health and Social State in Alsace), which is not on this map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.0field-weighted citation impact, top 14% 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.

NCT01663675 unknown statusnot on this map

Trisomy 21 in Adulthood. Evaluation of Health and Social State in Alsace (North-eastern France)

TypeobservationalSponsorUniversity Hospital, Strasbourg, FranceRan2014 to 2019Enrolled80ConditionsDown SyndromeArmskaryotype
3 · Its place in the literature

Who cites it

10 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. Inborn Errors of Adaptive Immunity in Down Syndrome.Journal of clinical immunology · 2020
    Review
  9. Article
  10. 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

6 authors at 1 institution in 1 country.

Aurélien GuffroyDepartment of Clinical Immunology and Internal Medicine, National Reference Center for Autoimmune Diseases, Hôpitaux Universitaires de Strasbourg, 1, place de l'Hôpital, 67091, Strasbourg, France. aurelien.guffroy@chru-strasbourg.fr.ORCID 0000-0003-0615-5305
Yannick DieudonnéDepartment of Clinical Immunology and Internal Medicine, National Reference Center for Autoimmune Diseases, Hôpitaux Universitaires de Strasbourg, 1, place de l'Hôpital, 67091, Strasbourg, France.
Beatrice Uring-LambertDepartment of Immunobiology, Hôpitaux Universitaires de Strasbourg, 67091, Strasbourg, France.
Joelle GoetzDepartment of Immunobiology, Hôpitaux Universitaires de Strasbourg, 67091, Strasbourg, France.
Yves AlembikDepartment of Clinical Genetic, Hôpitaux Universitaires de Strasbourg, 67091, Strasbourg, France.
Anne-Sophie KorganowDepartment of Clinical Immunology and Internal Medicine, National Reference Center for Autoimmune Diseases, Hôpitaux Universitaires de Strasbourg, 1, place de l'Hôpital, 67091, Strasbourg, France.
Hôpitaux Universitaires de Strasbourg · FR

Funding

Ministère des Affaires Sociales et de la Santé PHRC 2012-A00466-37Union Européenne This work was supported by grants from EU-funded (ERDF) project INTERREG V "RARENET".
6 · The paper itself

Abstract

backgroundDown syndrome (DS) is the most common form of viable chromosomal abnormality. DS is associated with recurrent infections, auto-immunity and malignancies in children. Little is known about immunity and infections in DS at adulthood.

methodsWe studied two separate group of adults (> 18 years old) with DS in a single referral tertiary center (Strasbourg University Hospital). The first group included 37 ambulatory DS patients between November 2014 and May 2017. We analyzed exhaustive serological and immunobiological parameters, at one point, together with the prevalence of infections, autoimmune manifestations and malignancies. The second group included 64 hospitalized patients (138 stays) in the same center, between January 2005 and December 2016.

resultsOne hundred and one adult patients with DS were included. Unlike children and despite a global lymphopenia, adults with DS underwent few infections in our ambulatory group. They did not experience any malignancy and, apart from hypothyroidism, they presented only occasional autoimmune manifestations. Hospitalized DS patients were older than ambulatory ones (median age 47 years (18-73) vs. 27 (18-52), p < 0.0001) and admitted mostly for infections (76.8%). Infections were associated with epilepsy and dementia (OR 6.5 (2.2-19), p = 0.001; p = 0.0006 in multivariate analysis) and higher mortality (OR 7.4 (1.4-37), p = 0.01).

conclusionDespite persistent immunobiological abnormalities at adulthood, young ambulatory adults with DS remain healthy with a low rate of infections. Infections are associated with neurological degeneration and increase the mortality arguing for a dedicated support of older DS patients.

trial registrationClinicalTrials.gov: NCT01663675 (August 13, 2012). Hospital Clinical Research Program (PHRC): number 2012-A00466-37 (Dr Y. Alembik).

Indexed as

AdolescentAdultAgedChromosome AberrationsDown SyndromeFemaleHospitalizationHumansLymphopeniaMaleMiddle AgedRetrospective StudiesYoung AdultAdultDown syndromeImmunodeficiencyInfectious riskNeurological impairment

Identifiers

PMID30634988
PMCPMC6329099
OpenAlexW2917367173

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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.