Evidence map›Paper›PMID 42426663›Full record

Observational studyBMC nephrology2026

Features and management of kidney manifestations of tuberous sclerosis complex: a real-world study in a Brazilian patient cohort.

Aline Grosskopf Monich, Elieser Hitoshi Watanabe, Mariana Faucz Munhoz da Cunha, Luciana Amaral Haddad, Andrei Odevar Cêa, Renan Pizza Terasoto, Gabriela Duarte Neves, Laís Faria Masulk Cardozo, Sérgio Antonio Antoniuk, Luiz Fernando Onuchic and 2 more

Abstract readObservational Study
In one paragraph

Observational study in BMC nephrology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Aline Grosskopf MonichDepartamento de Clínica Médica, Programa de Pós-Graduação em Medicina Interna e Ciências da Saúde, Universidade Federal do Paraná, Curitiba, PR, Brazil.ORCID http://orcid.org/0000-0002-7256-6674
Elieser Hitoshi WatanabeDivisão de Nefrologia, Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo, São Paulo, SP, Brasil.ORCID http://orcid.org/0000-0002-3371-6019
Mariana Faucz Munhoz da CunhaDepartamento de Pediatria, Hospital de Clínicas da Universidade Federal do Paraná, Curitiba, PR, Brazil.ORCID http://orcid.org/0000-0002-8901-5553
Luciana Amaral HaddadDepartment of Genetics and Evolutionary Biology, Instituto de Biociências, Universidade de São Paulo, São Paulo, SP, Brazil.ORCID http://orcid.org/0000-0003-1043-8981
Andrei Odevar CêaUniversidade Federal do Paraná, Curitiba, PR, Brazil.ORCID http://orcid.org/0009-0006-5817-534X
Renan Pizza TerasotoUniversidade Federal do Paraná, Curitiba, PR, Brazil.ORCID http://orcid.org/0009-0008-2783-0094
Gabriela Duarte NevesServiço de Nefrologia, Hospital de Clínicas da Universidade Federal do Paraná, Curitiba, PR, Brazil.ORCID http://orcid.org/0009-0008-7028-202X
Laís Faria Masulk CardozoUniversidade Federal do Paraná, Programa de Pós-Graduação em Saúde da Criança e do Adolescente, Curitiba, PR, Brazil.ORCID http://orcid.org/0000-0002-8674-4152
Sérgio Antonio AntoniukCentro de Neurologia Pediátrica, Hospital de Clínicas, Universidade Federal do Paraná, Curitiba, PR, Brazil.ORCID http://orcid.org/0000-0002-0678-3339
Luiz Fernando OnuchicDivisões de Medicina Molecular e Nefrologia, Faculdade de Medicina da Universidade de São Paulo, São Paulo, Brasil.ORCID http://orcid.org/0000-0002-4053-5419
John J BisslerDepartment of Pediatrics, University of Tennessee Health Science Center, Le Bonheur Children's Hospital, St. Jude Children's Research Hospital, Memphis, TN, USA.ORCID http://orcid.org/0000-0001-9685-9183
Fellype Carvalho BarretoDepartamento de Clínica Médica, Programa de Pós-Graduação em Medicina Interna e Ciências da Saúde, Universidade Federal do Paraná, Curitiba, PR, Brazil. fellype.barreto@ufpr.br.ORCID http://orcid.org/0000-0002-6394-9227

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTuberous sclerosis complex (TSC) is a rare autosomal dominant disorder resulting from pathogenic variants in the TSC1 or TSC2 genes, leading to hyperactivation of the mechanistic target of rapamycin (mTOR) pathway and subsequent development of benign neoplasms in multiple organs. Kidney involvement is frequent, being angiomyolipoma the most common lesion. Angiomyolipoma can occur since childhood and progress throughout life, potentially leading to complications such as hemorrhage and chronic kidney disease (CKD). This study aims to characterize the kidney phenotype in a Brazilian cohort of TSC patients and identify potential risk factors associated with kidney complications.

methodsThis real-world retrospective observational study analyzed data from TSC patients recorded on their first nephrology consultation at two Brazilian university hospitals between September 2019 and August 2024. Clinical, laboratory and imaging data were collected from medical records. Comparative analyses were conducted based on sex, history of kidney hemorrhage, kidney invasive interventions and CKD G3-G5D.

results172 patients were included (28 ± 14.2 years, 62.2% female, 22.7% pediatric). Angiomyolipoma was the most frequent renal lesion (91.7%) with increasing prevalence with age, followed by cysts (45.2%). 41.9% of the patients meeting renal indications were receiving mTOR inhibitor. The prevalence of CKD G3-G5, kidney hemorrhage and interventions was 9.9%, 16.6%, and 27.9%, respectively. Comparative analysis matched by age showed that female patients have slightly lower eGFR (117 [94-127] vs. 126 [97-149] mL/min/1.73m

conclusionsThis Brazilian cohort study demonstrated that TSC-related kidney involvement may occur early in life, displays a progressive profile and leads to severe kidney outcomes. The high rates of kidney complications and the suboptimal utilization of mTOR inhibitors underscore the need to increase awareness, early referral to nephrologist and timely therapeutic intervention.

Indexed as

AngiomyolipomaKidney NeoplasmsRenal Insufficiency, ChronicTuberous SclerosisAdolescentAdultBrazilChildCohort StudiesFemaleHumansMaleMiddle AgedMTOR InhibitorsRetrospective StudiesYoung AdultMTOR InhibitorsAngiomyolipomaChronic kidney diseasemTOR InhibitorsTuberous sclerosis complex

Identifiers

PMID42426663
PMCPMC13640161

What Socratic holds

Textmetadata
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 Socratic graph.