Evidence map›Paper›PMID 39529988›Full record

ArticleArchives of endocrinology and metabolism2024

Association between the G/G genotype of the lncRNA

Leticia de Almeida Brondani, Isabele Dandolini, Eliandra Girardi, Luís Henrique Canani, Daisy Crispim, Cristine Dieter

Abstract read
In one paragraph

Article in Archives of endocrinology and metabolism, 2024. 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

6 authors.

Leticia de Almeida BrondaniUnidade de Pesquisa Laboratorial Centro de Pesquisa Experimental Hospital de Clínicas de Porto Alegre Porto AlegreRS Brasil Unidade de Pesquisa Laboratorial, Centro de Pesquisa Experimental, Hospital de Clínicas de Porto Alegre, Porto Alegre, RS, Brasil.ORCID https://orcid.org/0000-0003-0837-2645
Isabele DandoliniHospital de Clínicas de Porto Alegre Serviço de Endocrinologia Porto AlegreRS Brasil Serviço de Endocrinologia, Hospital de Clínicas de Porto Alegre, Porto Alegre, RS, Brasil.ORCID https://orcid.org/0009-0000-2900-322X
Eliandra GirardiHospital de Clínicas de Porto Alegre Serviço de Endocrinologia Porto AlegreRS Brasil Serviço de Endocrinologia, Hospital de Clínicas de Porto Alegre, Porto Alegre, RS, Brasil.ORCID https://orcid.org/0000-0003-4485-0202
Luís Henrique CananiHospital de Clínicas de Porto Alegre Serviço de Endocrinologia Porto AlegreRS Brasil Serviço de Endocrinologia, Hospital de Clínicas de Porto Alegre, Porto Alegre, RS, Brasil.ORCID https://orcid.org/0000-0002-1813-4491
Daisy CrispimHospital de Clínicas de Porto Alegre Serviço de Endocrinologia Porto AlegreRS Brasil Serviço de Endocrinologia, Hospital de Clínicas de Porto Alegre, Porto Alegre, RS, Brasil.ORCID https://orcid.org/0000-0001-5095-9269
Cristine DieterHospital de Clínicas de Porto Alegre Serviço de Endocrinologia Porto AlegreRS Brasil Serviço de Endocrinologia, Hospital de Clínicas de Porto Alegre, Porto Alegre, RS, Brasil.ORCID https://orcid.org/0000-0003-2765-930X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: To investigate the association between the long noncoding RNAs (lncRNAs) Subjects and methods: The study included 628 patients with T2DM and DR ("case group," including 283 with proliferative DR [PDR] and 345 with nonproliferative DR [NPDR]), and 381 patients with T2DM but no DR ("control group"). The diagnosis of DR was established using indirect ophthalmoscopy. The rs7158663 A/G polymorphism was genotyped using real-time polymerase chain reaction (PCR) with TaqMan probes. Results: Patients with DR, compared with those without DR, had lower frequencies of both the G/G genotype (17.5% and 23.6%, respectively, p = 0.044) and the G allele (p = 0.017). When only patients with PDR were compared with controls, the G/G genotype was associated with increased protection against PDR after adjustment (odds ratio 0.551, 95% confidence interval 0.314-0.966, p = 0.038). This association also remained in the dominant (p = 0.036) and additive (p = 0.031) genetic models. Conclusion: This study reveals, for the first time, that the G/G genotype of the lncRNA

Indexed as

Diabetes Mellitus, Type 2Diabetic RetinopathyGenetic Predisposition to DiseaseGenotypePolymorphism, Single NucleotideRNA, Long NoncodingAgedAllelesCase-Control StudiesFemaleGene FrequencyHumansMaleMiddle AgedMEG3 non-coding RNA, humanRNA, Long NoncodingDiabetic retinopathylncRNA MEG3polymorphisms

Identifiers

PMID39529988
PMCPMC11554361

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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.