Evidence map›Paper›PMID 36153588›Full record

ArticleDiabetology & metabolic syndrome2022

Reduced gut microbiota diversity in patients with congenital generalized lipodystrophy.

Renan Magalhães Montenegro Junior, Clarisse Mourão Melo Ponte, Maria Helane Costa Gurgel Castelo, Alessandro Conrado de Oliveira Silveira, Virgínia Oliveira Fernandes, Catarina Brasil D'Alva, Luiz Felipe Valter Oliveira, Angélica Domingues Hristov, Silviane Praciano Bandeira, Grayce Ellen da Cruz Paiva and 1 more

Open access · goldAbstract read
In one paragraph

Article in Diabetology & metabolic syndrome, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.9field-weighted citation impact, top 22% 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

6 citing papers in PubMed, 8 citations in OpenAlex.

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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

11 authors at 2 institutions in 1 country.

Renan Magalhães Montenegro JuniorUniversity Hospitals, Federal University of Ceará/Ebserh, Fortaleza, CE, Brazil.
Clarisse Mourão Melo PonteUniversity Hospitals, Federal University of Ceará/Ebserh, Fortaleza, CE, Brazil. clarisse.ponte@unicrhistus.edu.br.
Maria Helane Costa Gurgel CasteloUniversity Hospitals, Federal University of Ceará/Ebserh, Fortaleza, CE, Brazil.
Alessandro Conrado de Oliveira SilveiraDASA, São Paulo, SP, Brazil.
Virgínia Oliveira FernandesUniversity Hospitals, Federal University of Ceará/Ebserh, Fortaleza, CE, Brazil.
Catarina Brasil D'AlvaUniversity Hospitals, Federal University of Ceará/Ebserh, Fortaleza, CE, Brazil.
Luiz Felipe Valter OliveiraBiomeHub, Florianópolis, SC, Brazil.
Angélica Domingues HristovDASA, São Paulo, SP, Brazil.
Silviane Praciano BandeiraDASA, São Paulo, SP, Brazil.
Grayce Ellen da Cruz PaivaUniversity Hospitals, Federal University of Ceará/Ebserh, Fortaleza, CE, Brazil.
José Eduardo LeviDASA, São Paulo, SP, Brazil.
Universidade Federal do Ceará · BRUniversidade Regional de Blumenau · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPrevious studies suggest intestinal dysbiosis is associated with metabolic diseases. However, the causal relationship between them is not fully elucidated. Gut microbiota evaluation of patients with congenital generalized lipodystrophy (CGL), a disease characterized by the absence of subcutaneous adipose tissue, insulin resistance, and diabetes since the first years of life, could provide insights into these relationships.

methodsA cross-sectional study was conducted with patients with CGL (n = 17) and healthy individuals (n = 17). The gut microbiome study was performed by sequencing the 16S rRNA gene through High-Throughput Sequencing (BiomeHub Biotechnologies, Brazil).

resultsThe median age was 20.0 years old, and 64.7% were female. There was no difference between groups in pubertal stage, BMI, ethnicity, origin (rural or urban), delivery, breastfeeding, caloric intake, macronutrient, or fiber consumption. Lipodystrophic patients presented a lower alpha diversity (Richness index: 54.0 versus 67.5; p = 0.008). No differences were observed in the diversity parameters when analyzing the presence of diabetes, its complications, or the CGL subtype.

conclusionIn this study, we demonstrate for the first time a reduced gut microbiota diversity in individuals with CGL. Dysbiosis was present despite dietary treatment and was also observed in young patients. Our findings allow us to speculate that the loss of intestinal microbiota diversity may be due to metabolic abnormalities present since the first years of life in CGL. Longitudinal studies are needed to confirm these findings, clarifying the possible causal link between dysbiosis and insulin resistance in humans.

Indexed as

DiabetesGut microbiotaLipodystrophy

Identifiers

PMID36153588
PMCPMC9508722
OpenAlexW4296982910

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.