Evidence map›Paper›PMID 35898389›Full record

ArticleInternational journal of nephrology2022

Renal Amyloidosis: Epidemiological, Clinical, and Laboratory Profile in Adults from One Nephrology Center.

Hayet Kaaroud, Amel Harzallah, Mariem Hajji, Soumaya Chargui, Samia Barbouch, Sami Turki, Raja Trabelsi, Rim Goucha, Fatma Ben Moussa, Hedi Ben Maiz and 2 more

Open access · goldAbstract read
In one paragraph

Article in International journal of nephrology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.6field-weighted citation impact, top 36% 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

1 citing paper in PubMed, 8 citations in OpenAlex.

  1. 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

12 authors at 1 institution in 1 country.

Hayet KaaroudDepartment of Medicine A, Charles Nicolle Hospital, Tunis, Tunisia.
Amel HarzallahDepartment of Medicine A, Charles Nicolle Hospital, Tunis, Tunisia.ORCID https://orcid.org/0000-0001-6816-4261
Mariem HajjiDepartment of Medicine A, Charles Nicolle Hospital, Tunis, Tunisia.
Soumaya CharguiDepartment of Medicine A, Charles Nicolle Hospital, Tunis, Tunisia.
Samia BarbouchDepartment of Medicine A, Charles Nicolle Hospital, Tunis, Tunisia.
Sami TurkiDepartment of Medicine A, Charles Nicolle Hospital, Tunis, Tunisia.
Raja TrabelsiDepartment of Medicine A, Charles Nicolle Hospital, Tunis, Tunisia.
Rim GouchaLaboratory of Renal Pathology LR00SP01, Charles Nicolle Hospital, Tunis, Tunisia.
Fatma Ben MoussaFaculty of Medicine of Tunis, University of Tunis, El Manar, Tunis, Tunisia.
Hedi Ben MaizFaculty of Medicine of Tunis, University of Tunis, El Manar, Tunis, Tunisia.
Fethi Ben HamidaDepartment of Medicine A, Charles Nicolle Hospital, Tunis, Tunisia.
Ezzeddine AbderrahimDepartment of Medicine A, Charles Nicolle Hospital, Tunis, Tunisia.
Tunis University · TN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Renal amyloidosis is one of the main differential diagnoses of nephrotic proteinuria in adults and the elderly. The aim of this study with the most important series in our country is to contribute to the epidemiological, clinical, and etiological study of the renal amyloidosis. Methods: In a retrospective study carried out between 1975 and 2019, 310 cases of histologically proven and typed renal amyloidosis were selected for this study. Results: There were 209 men and 101 women with a mean age of 53.8 ± 15.4 years (range, 17-84 years). Of the 310 cases, 255 (82.3%) were diagnosed with AA renal amyloidosis and 55 (17.7%) with non-AA amyloidosis. Infections were the main cause of AA amyloidosis, and tuberculosis was the most frequent etiology. The period from the onset of the underlying disease to diagnosis of the renal amyloidosis was an average of 177 months. The most frequent manifestations at the time of diagnosis were nephrotic syndrome (84%), chronic renal failure (30.3%), and end-stage renal disease (37.8%). After a medium follow-up of 16 months (range, 0-68 months), mortality occurred in 60 cases. Conclusions: Given the high frequency of AA amyloidosis in our country, awareness of the proper management of infectious and chronic inflammatory diseases remains a priority in reducing the occurrence of this serious disease.

Identifiers

PMID35898389
PMCPMC9314002
OpenAlexW4285800676

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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.