Evidence map›Paper›PMID 32342491›Full record

ArticleBritish journal of haematology2020

The natural course of pregnancies in women with primary atypical haemolytic uraemic syndrome and asymptomatic relatives.

Sjoerd A M E G Timmermans, Alexis Werion, Marc E A Spaanderman, Chris P Reutelingsperger, Jan G M C Damoiseaux, Johann Morelle, Pieter van Paassen

Open access · hybridAbstract read
In one paragraph

Article in British journal of haematology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
0.9field-weighted citation impact, top 27% 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

8 citing papers in PubMed, 1 synthesis or guideline pooled it, 17 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Etiology and outcomes: Thrombotic microangiopathies in pregnancy.Research and practice in thrombosis and haemostasis · 2023
    Article
  5. Article
  6. Review
  7. Review
  8. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 2 institutions in 2 countries.

Sjoerd A M E G TimmermansDepartment of Nephrology and Clinical Immunology, Maastricht University Medical Center, Maastricht, the Netherlands.ORCID 0000-0001-5925-2753
Alexis WerionDivision of Nephrology, Cliniques Universitaires Saint-Luc, Brussels, Belgium.
Marc E A SpaandermanDepartment of Obstetrics and Gynecology, Maastricht University Medical Center, Maastricht, the Netherlands.
Chris P ReutelingspergerDepartment of Biochemistry, Cardiovascular Research Institute Maastricht (CARIM), Maastricht University, Maastricht, the Netherlands.
Jan G M C DamoiseauxDepartment of Central Diagnostic Laboratory, Maastricht University Medical Center, Maastricht, the Netherlands.
Johann MorelleDivision of Nephrology, Cliniques Universitaires Saint-Luc, Brussels, Belgium.
Pieter van PaassenDepartment of Nephrology and Clinical Immunology, Maastricht University Medical Center, Maastricht, the Netherlands.
Maastricht University · NLCliniques Universitaires Saint-Luc · BE

Funding

Association pour l'Information et la Recherche sur les Maladies Rénales GénétiquesFondation Saint-LucFonds de Recherche des Cliniques Universitaires Saint-LucNational Fund for Scientific Research
6 · The paper itself

Abstract

Pregnancy has been linked to various microangiopathies, including primary atypical haemolytic uraemic syndrome (aHUS). Complement dysregulation, often linked to rare variants in complement genes, is key for primary aHUS to manifest and may play a role in pregnancy complications of the mother and fetus. The burden of such complications is unknown, making counselling of women with primary aHUS and asymptomatic relatives difficult. We analyzed the maternal and fetal outcomes of 39 pregnancies from 17 women with primary aHUS and two asymptomatic relatives. Seven out of 39 pregnancies were complicated by pregnancy-associated aHUS. Five out of 32 pregnancies not linked to pregnancy-associated aHUS were complicated by pre-eclampsia or HELLP. Rare genetic variants were identified in 10 women (asymptomatic relatives, n = 2) who had a total of 14 pregnancies, including 10 uncomplicated pregnancies. Thirty-five out of 39 pregnancies resulted in live birth. Eight out of 19 women had progressed to end-stage kidney disease, with an incidence of 2·95 (95% confidence interval, 1·37-5·61) per 100 person-years after the first pregnancy. Thus, we emphasized the frequency of successful pregnancies in women with primary aHUS and asymptomatic relatives. Pregnancies should be monitored closely. Rare genetic variants cannot predict the risk of a given pregnancy.

Indexed as

Polymorphism, Single NucleotideAbortion, SpontaneousAllelesAsymptomatic DiseasesAtypical Hemolytic Uremic SyndromeFamilyFemaleGene FrequencyGestational AgeHELLP SyndromeHumansInfant, NewbornLive BirthMultiplex Polymerase Chain ReactionPre-EclampsiaPregnancycomplementgeneticspregnancyprimary atypical haemolytic uraemic syndromethrombotic microangiopathy

Identifiers

PMID32342491
PMCPMC7496636
OpenAlexW3018030806

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.