Evidence map›Paper›PMID 27383202›Full record

ArticlePloS one2016

Thrombotic Thrombocytopenic Purpura in Black People: Impact of Ethnicity on Survival and Genetic Risk Factors.

Suella Martino, Mathieu Jamme, Christophe Deligny, Marc Busson, Pascale Loiseau, Elie Azoulay, Lionel Galicier, Frédéric Pène, François Provôt, Antoine Dossier and 4 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
28citing 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

28 citing papers in PubMed, 1 synthesis or guideline pooled it, 56 citations in OpenAlex.

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  19. Autoimmune-mediated renal disease and hypertension.Clinical science (London, England : 1979) · 2021
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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

14 authors at 8 institutions in 2 countries.

Suella MartinoService d'Hématologie, Hôpital Saint-Antoine, AP-HP, Paris, France.
Mathieu JammeCentre de Référence des Microangiopathies Thrombotiques, Hôpital Saint-Antoine, AP-HP, et UPMC Univ Paris 06, Paris, France.
Christophe DelignyService de Médecine interne, CHU de Fort-de France, Fort-de-France, Martinique, France.
Marc BussonAP-HP, Laboratoire Jean Dausset d'Immunologie et d'Histocompatibilité & INSERM, UMRS 1160, Hôpital Saint Louis, Sorbonne Paris Cité, Paris, France.
Pascale LoiseauAP-HP, Laboratoire Jean Dausset d'Immunologie et d'Histocompatibilité & INSERM, UMRS 1160, Hôpital Saint Louis, Sorbonne Paris Cité, Paris, France.
Elie AzoulayCentre de Référence des Microangiopathies Thrombotiques, Hôpital Saint-Antoine, AP-HP, et UPMC Univ Paris 06, Paris, France.
Lionel GalicierCentre de Référence des Microangiopathies Thrombotiques, Hôpital Saint-Antoine, AP-HP, et UPMC Univ Paris 06, Paris, France.
Frédéric PèneCentre de Référence des Microangiopathies Thrombotiques, Hôpital Saint-Antoine, AP-HP, et UPMC Univ Paris 06, Paris, France.
François ProvôtCentre de Référence des Microangiopathies Thrombotiques, Hôpital Saint-Antoine, AP-HP, et UPMC Univ Paris 06, Paris, France.
Antoine DossierCentre de Référence des Microangiopathies Thrombotiques, Hôpital Saint-Antoine, AP-HP, et UPMC Univ Paris 06, Paris, France.
Samir SahebCentre de Référence des Microangiopathies Thrombotiques, Hôpital Saint-Antoine, AP-HP, et UPMC Univ Paris 06, Paris, France.
Agnès VeyradierCentre de Référence des Microangiopathies Thrombotiques, Hôpital Saint-Antoine, AP-HP, et UPMC Univ Paris 06, Paris, France.
Paul CoppoService d'Hématologie, Hôpital Saint-Antoine, AP-HP, Paris, France.
French Reference Center for Thrombotic Microangiopathies
Hôpital Saint-Antoine · FRAssistance Publique – Hôpitaux de Paris · FRSorbonne Université · FRCentre Hospitalier Universitaire de Martinique · MQDélégation Paris 7 · FRHôpital Saint-Louis · FRInserm · FRSorbonne Paris Cité · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Black people are at increased risk of thrombotic thrombocytopenic purpura (TTP). Whether clinical presentation of TTP in Black patients has specific features is unknown. We assessed here differences in TTP presentation and outcome between Black and White patients. Clinical presentation was comparable between both ethnic groups. However, prognosis differed with a lower death rate in Black patients than in White patients (2.7% versus 11.6%, respectively, P = .04). Ethnicity, increasing age and neurologic involvement were retained as risk factors for death in a multivariable model (P < .05 all). Sixty-day overall survival estimated by the Kaplan-Meier curves and compared with the Log-Rank test confirmed that Black patients had a better survival than White patients (P = .03). Salvage therapies were similarly performed between both groups, suggesting that disease severity was comparable. The comparison of HLA-DRB1*11, -DRB1*04 and -DQB1*03 allele frequencies between Black patients and healthy Black individuals revealed no significant difference. However, the protective allele against TTP, HLA-DRB1*04, was dramatically decreased in Black individuals in comparison with White individuals. Black people with TTP may have a better survival than White patients despite a comparable disease severity. A low natural frequency of HLA-DRB1*04 in Black ethnicity may account for the greater risk of TTP in this population.

Indexed as

AdultAllelesBlack or African AmericanBlack PeopleFemaleGene FrequencyHLA-DQ beta-ChainsHLA-DRB1 ChainsHumansKaplan-Meier EstimateMaleMiddle AgedPurpura, Thrombotic ThrombocytopenicRegistriesRisk FactorsTreatment OutcomeHLA-DQB1 antigenHLA-DQ beta-ChainsHLA-DRB1*04 antigenHLA-DRB1*11 antigenHLA-DRB1 Chains

Identifiers

PMID27383202
PMCPMC4934773
OpenAlexW2475364998

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.