Evidence map›Paper›PMID 35057750›Full record

ArticleBMC nephrology2022

What is the impact of blood pressure on neurological symptoms and the risk of ESKD in primary and secondary thrombotic microangiopathies based on clinical presentation: a retrospective study.

Jean-Michel Halimi, Benjamin Thoreau, Florent von Tokarski, Adeline Bauvois, Juliette Gueguen, Nicolas Goin, Christelle Barbet, Sylvie Cloarec, Elodie Mérieau, Sébastien Lachot and 13 more

Open access · goldAbstract read
In one paragraph

Article in BMC nephrology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.1field-weighted citation impact, top 25% 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

5 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
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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

23 authors at 6 institutions in 2 countries.

Jean-Michel HalimiService de Néphrologie-HTA, Dialyses, Transplantation Rénale, Hôpital Bretonneau et hôpital Clôcheville, CHU Tours, 2 Bd Tonnellé, 37044, Tours Cedex, France. halimi@med.univ-tours.fr.
Benjamin ThoreauService de Néphrologie-HTA, Dialyses, Transplantation Rénale, Hôpital Bretonneau et hôpital Clôcheville, CHU Tours, 2 Bd Tonnellé, 37044, Tours Cedex, France.
Florent von TokarskiService de Néphrologie-HTA, Dialyses, Transplantation Rénale, Hôpital Bretonneau et hôpital Clôcheville, CHU Tours, 2 Bd Tonnellé, 37044, Tours Cedex, France.
Adeline BauvoisService de Néphrologie-HTA, Dialyses, Transplantation Rénale, Hôpital Bretonneau et hôpital Clôcheville, CHU Tours, 2 Bd Tonnellé, 37044, Tours Cedex, France.
Juliette GueguenService de Néphrologie-HTA, Dialyses, Transplantation Rénale, Hôpital Bretonneau et hôpital Clôcheville, CHU Tours, 2 Bd Tonnellé, 37044, Tours Cedex, France.
Nicolas GoinService de Néphrologie-HTA, Dialyses, Transplantation Rénale, Hôpital Bretonneau et hôpital Clôcheville, CHU Tours, 2 Bd Tonnellé, 37044, Tours Cedex, France.
Christelle BarbetService de Néphrologie-HTA, Dialyses, Transplantation Rénale, Hôpital Bretonneau et hôpital Clôcheville, CHU Tours, 2 Bd Tonnellé, 37044, Tours Cedex, France.
Sylvie CloarecService de Néphrologie-HTA, Dialyses, Transplantation Rénale, Hôpital Bretonneau et hôpital Clôcheville, CHU Tours, 2 Bd Tonnellé, 37044, Tours Cedex, France.
Elodie MérieauService de Néphrologie-HTA, Dialyses, Transplantation Rénale, Hôpital Bretonneau et hôpital Clôcheville, CHU Tours, 2 Bd Tonnellé, 37044, Tours Cedex, France.
Sébastien LachotService d'Hématologie Biologique, Hôpital Bretonneau, CHU Tours, Tours, France.
Denis GarotService de Médecine Intensive Réanimation, Hôpital Bretonneau, CHU Tours, Tours, France.
Adrien LemaignenService de Maladies Infectieuses, Hôpital Bretonneau, CHU Tours, Tours, France.
Emmanuel GyanService d'Hématologie et Thérapie Cellulaire, Hôpital Bretonneau, CHU Tours; ERL CNRS 7001, Université de Tours, Tours, France.
Franck PerrotinService de Gynécologie Obstétrique B, Maternité Olympe de Gouges, Hôpital Bretonneau, CHU Tours, Inserm U1253 « Imaging and Brain », François-Rabelais University, Tours, France.
Claire PouplardLaboratoire d'Hématologie-Hémostase, Hôpital Trousseau, CHU Tours, Tours, France.
François MaillotService de Médecine interne, Hôpital Bretonneau, CHU Tours, Tours, France.
Philippe GataultService de Néphrologie-HTA, Dialyses, Transplantation Rénale, Hôpital Bretonneau et hôpital Clôcheville, CHU Tours, 2 Bd Tonnellé, 37044, Tours Cedex, France.
Bénédicte SautenetService de Néphrologie-HTA, Dialyses, Transplantation Rénale, Hôpital Bretonneau et hôpital Clôcheville, CHU Tours, 2 Bd Tonnellé, 37044, Tours Cedex, France.
Emmanuel RuschLaboratoire de Santé Publique, Hôpital Bretonneau, CHU Tours, Tours, France.
Véronique Frémeaux-BacchiLaboratoire d'Immunologie, Hôpital Européen Georges Pompidou, Paris, France.
Cécile VigneauCHU Pontchaillou, service de néphrologie, 35033 Rennes, Université Rennes 1, Inserm IRSET, UMR 1085, 35033, Rennes, France.
Guillaume BayerService de Néphrologie-HTA, Dialyses, Transplantation Rénale, Hôpital Bretonneau et hôpital Clôcheville, CHU Tours, 2 Bd Tonnellé, 37044, Tours Cedex, France.
Fadi FakhouriService of nephrology, department of medicine, CHUV and Université de Lausanne, Lausanne, Switzerland.
Centre Hospitalier Universitaire de Tours · FRBretonneau Hospital · FRUniversité de Tours · FRHôpital Européen · FRInserm · FRUniversity of Lausanne · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe impact of blood pressure on neurological symptoms and risk of end-stage kidney disease (ESKD) is unknown in primary and secondary thrombotic microangiopathies (TMAs).

methodsWe measured baseline systolic (SBP) and diastolic (DBP) BP in consecutive 563 patients with adjudicated primary and secondary TMAs, and assessed its association with the risk of ESKD.

resultsNormal BP, grade 1, 2 and 3 hypertension were present in 243 (43.1%), 132 (23.4%), 101 (17.9%) and 88 (15.6%), respectively. Significant BP differences were noted in relation to the cause of TMA: highest BP values were found in patients with atypical hemolytic-uremic syndrome (aHUS), pregnancy, transplantation and auto-immune-related TMAs. Normal BP or grade 1 hypertension was found in 17/18 (94.4%) patients with thrombotic thrombocytopenic patients (only 1/18 (5.6%) had a SBP value>150 mmHg). In contrast, BP values could not differentiate isolated "essential" malignant hypertension (MH) from MH associated with aHUS (isolated MH (n=15): BP (median (IQR)): 220 (182-249)/132 (101-150) mmHg; MH with aHUS (n=5): BP: 223 (196-245)/131 (111-144) mmHg). The risk of vigilance disturbances (6.9%, 15.0%, 25.0%, respectively), epileptic seizures (1.5%, 4.0%, 12.5%, respectively) and posterior reversible encephalopathy syndrome (0.76%, 2.97%, 6.82%, respectively) increased with increasing baseline BP values from grade 1 to grade 3 hypertension. ESKD occurred in 35/563 (6.2%) patients (1.23%, 2.27%, 11.9% and 19.3% of patients with normal BP, grade 1, 2 and 3 hypertension, respectively). As compared to patients with normal BP (<120/139 mmHg), grade 1, grade 2 and grade 3 hypertension were associated with a greater risk of ESKD in univariate (OR: 1.91 [0.83-4.40], 13.2 [3.56-48.9] and 34.8 [9.31-130], respectively) and multivariate (OR: 0.89 [0.30-2.69], 7.00 [1.57-31.3] and 19.7 [4.53-85.2], respectively) analyses. The association between BP and the risk of ESRD was unchanged after adjustment on eculizumab use (OR: 3.46 [1.41-8.49], 17.7 [4.44-70.0] and 70.6 [8.61-579], respectively). Patients with MH, regardless of its cause, had a greater risk of ESKD (OR: 26.4 [10.0-69.8] vs other patients).

conclusionsBaseline BP differs in primary and secondary TMAs. High BP reduces the neurological tolerance of TMAs and is a powerful independent risk factor of ESKD, even after adjustment on TMA's cause.

Indexed as

Blood PressureAdultFemaleHumansHypertensionKidney Failure, ChronicMaleMiddle AgedNervous System DiseasesRetrospective StudiesRisk AssessmentThrombotic MicroangiopathiesYoung AdultBlood pressureepidemiologyESKDhypertensionneurological symptomsposterior reversible encephalopathy syndromethrombotic microangiopathy

Identifiers

PMID35057750
PMCPMC8781095
OpenAlexW4206082397

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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.