Evidence map›Paper›PMID 40503657›Full record

ArticleJournal of clinical laboratory analysis2025

Mitochondrial tRNA

Xiaojuan Rao, Liran Xie, Shuangwei Shi, Yifan Fang

Abstract read
In one paragraph

Article in Journal of clinical laboratory analysis, 2025. 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
–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

1 citing paper in PubMed.

  1. Mitochondrial tRNA-Derived Diseases.International journal of molecular sciences · 2025
    Review
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

4 authors.

Xiaojuan RaoDepartment of Endocrinology, The Fifth Affiliated Hospital of Zhengzhou University, Zhengzhou, People's Republic of China.ORCID https://orcid.org/0009-0004-6245-6764
Liran XieDepartment of Endocrinology, The Fifth Affiliated Hospital of Zhengzhou University, Zhengzhou, People's Republic of China.
Shuangwei ShiDepartment of Endocrinology, The Fifth Affiliated Hospital of Zhengzhou University, Zhengzhou, People's Republic of China.
Yifan FangDepartment of Endocrinology, The Fifth Affiliated Hospital of Zhengzhou University, Zhengzhou, People's Republic of China.

Funding

Medical Science and Technology Research Program of Henan Province LHGJ20200474
6 · The paper itself

Abstract

backgroundSequence alternations in mitochondrial genomes, especially in mitochondrial tRNA (mt-tRNA), are closely related to type 2 diabetes mellitus (T2DM); however, the detailed molecular mechanism is still largely undetermined.

methodsHerein, we reported a T2DM Chinese family by using molecular and biochemical analyses. The mtDNA mutations in this pedigree were detected by PCR and Sanger sequencing. Moreover, phylogenetic analysis was used to assess the pathogenic mitochondrial DNA (mtDNA) mutation. We further evaluated mt-tRNA stability levels and mitochondrial functions in cybrids with and without the m.14687A>G mutation.

resultsMembers of this family expressed variable clinical phenotypes. Screening for the entire mitochondrial genomes revealed the occurrence of a novel m.14687A>G mutation, which was located at position 60 in the TψC loop of tRNA

conclusionOur finding revealed that the novel m.14687A>G mutation resulted in aberrant mt-tRNA metabolism and mitochondrial dysfunctions, which should be regarded as a pathogenic mutation for T2DM.

Indexed as

Diabetes Mellitus, Type 2MutationAdultAgedDNA, MitochondrialFemaleHumansMaleMiddle AgedMitochondriaPedigreeDNA, MitochondrialChinese pedigreem.14687A>G mutationmitochondrial dysfunctionmitochondrial tRNAGluT2DM

Identifiers

PMID40503657
PMCPMC12217652

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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.