Evidence map›Paper›PMID 40630302›Full record

ArticleKidney international reports2025

Kidney Outcomes in Patients With Hereditary Transthyretin Amyloid Nephropathy Treated With Transthyretin Stabilizers And Gene-Silencer Therapies.

Julien Dang, Justine Solignac, Sophie Ferlicot, Charlotte Mussini, Frank Bridoux, Antoine Huart, Marie Essig, Delphine Campigli, Mickaël Bobot, Laurent Daniel and 15 more

Abstract read
In one paragraph

Article in Kidney international reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Review
  2. Article
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

25 authors.

Julien DangAssistance Publique des Hôpitaux de Paris, Hôpital Ambroise Paré, Service de Néphrologie et Dialyse, Boulogne-Billancourt, France.
Justine SolignacAix-Marseille Université, C2VN, INSERM, INRAE, Marseille, France - AP-HM, Hôpital de la Conception, Service de Néphrologie et Transplantation rénale, Marseille, France.
Sophie FerlicotAP-HP, Hôpital de Bicêtre, Service d'Anatomie Pathologique, Le Kremlin-Bicêtre, France.
Charlotte MussiniAP-HP, Hôpital de Bicêtre, Service d'Anatomie Pathologique, Le Kremlin-Bicêtre, France.
Frank BridouxHôpital de Poitiers, Service de Néphrologie, Hémodialyse et Transplantation rénale, Poitiers, France.
Antoine HuartService de Néphrologie et Transplantation d'organes, Hôpital Rangueil, Toulouse, France.
Marie EssigAssistance Publique des Hôpitaux de Paris, Hôpital Ambroise Paré, Service de Néphrologie et Dialyse, Boulogne-Billancourt, France.
Delphine CampigliAix-Marseille Université, C2VN, INSERM, INRAE, Marseille, France - AP-HM, Hôpital de la Conception, Service de Néphrologie et Transplantation rénale, Marseille, France.
Mickaël BobotAix-Marseille Université, C2VN, INSERM, INRAE, Marseille, France - AP-HM, Hôpital de la Conception, Service de Néphrologie et Transplantation rénale, Marseille, France.
Laurent DanielService d'Anatomie Pathologique, Hôpital de la Conception, Marseille, France.
Thibaud DamyService de Cardiologie, AP-HP, Hôpitaux Universitaires Henri Mondor, Créteil, France.
Violaine Planté-BordeneuveService de Neurologie, AP-HP, Hôpitaux Universitaires Henri Mondor, Créteil, France.
Hamza SakhiService de Néphrologie et Transplantation, AP-HP, Hôpitaux Universitaires Henri Mondor, Créteil, France.
Céline LabeyrieService de Neurologie, AP-HP, Hôpital de Bicêtre, Le Kremlin-Bicêtre, France.
Cécile CauquilService de Neurologie, AP-HP, Hôpital de Bicêtre, Le Kremlin-Bicêtre, France.
Andoni Echaniz-LagunaService de Neurologie, AP-HP, Hôpital de Bicêtre, Le Kremlin-Bicêtre, France.
Ilias KounisCentre Hépato-Biliaire, AP-HP, Hôpital Paul-Brousse, Villejuif, France.
Anissa MoktefiService d'Anatomie Pathologique, AP-HP, Hôpitaux Universitaires Henri Mondor, Créteil, France.
Perrine DevicService de Neurologie, Hospices Civils de Lyon, Hôpital Lyon Sud, Lyon, France.
Sarah MouawadAP-HP, Hôpital de Bicêtre, Service de Néphrologie et Transplantation, Le Kremlin-Bicêtre, France.
Albane Brodin-SartoriusAP-HP, Hôpital de Bicêtre, Service de Néphrologie et Transplantation, Le Kremlin-Bicêtre, France.
Renaud SnanoudjAP-HP, Hôpital de Bicêtre, Service de Néphrologie et Transplantation, Le Kremlin-Bicêtre, France.
Mohamad ZaidanAP-HP, Hôpital de Bicêtre, Service de Néphrologie et Transplantation, Le Kremlin-Bicêtre, France.
Noémie Jourde-ChicheAix-Marseille Université, C2VN, INSERM, INRAE, Marseille, France - AP-HM, Hôpital de la Conception, Service de Néphrologie et Transplantation rénale, Marseille, France.
Vincent AudardService de Néphrologie et Transplantation, AP-HP, Hôpitaux Universitaires Henri Mondor, Créteil, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Kidney involvement is underestimated in patients with hereditary transthyretin amyloidosis (ATTRv), and few data are available about the renal outcomes of patients treated with targeted therapies. Methods: Patients with ATTRv nephropathy (ATTRv-N) from 6 French referral centers were retrospectively included. The evolution of estimated glomerular filtration rate (eGFR) and proteinuria, and the specific treatments of ATTRv were collected. Renal survival was assessed by using a renal composite end point, including an eGFR decline > 50% from baseline and/or dialysis requirement. Results: Twenty-three patients (70% female) with a median age at ATTRv-N diagnosis of 50 (interquartile range [IQR]: 37-63) years were included. Baseline eGFR was 60 (39-83) ml/min per 1.73 m Conclusion: Our study highlights the underrecognized risk of chronic kidney disease (CKD) and end-stage kidney disease in ATTRv and suggests that siRNA could be a promising therapeutic option for the stabilization of kidney function.

Indexed as

gene silencinggenetic kidney diseaseglomerular diseasehereditary transthyretin amyloidosisnephrotic syndromesystemic amyloidosis

Identifiers

PMID40630302
PMCPMC12232965

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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.