Evidence map›Paper›PMID 37308566›Full record

ArticleJournal of human genetics2023

Genetic variants and altered expression of SERPINF1 confer disease susceptibility in patients with otosclerosis.

Neha Singh, Kirtal Hansdah, Amal Bouzid, Chinmay Sundar Ray, Ashim Desai, Khirod Chandra Panda, Jyotish Chandra Choudhury, Adel Tekari, Saber Masmoudi, Puppala Venkat Ramchander

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Article in Journal of human genetics, 2023. 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
0.7field-weighted citation impact, top 30% 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

0 citing papers in PubMed, 2 citations in OpenAlex.

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

10 authors at 4 institutions in 3 countries.

Neha SinghInstitute of Life Sciences, Nalco Square, Chandrasekharpur, Bhubaneswar, India.
Kirtal HansdahInstitute of Life Sciences, Nalco Square, Chandrasekharpur, Bhubaneswar, India.
Amal BouzidLaboratory of Molecular and Cellular Screening Processes, Centre of Biotechnology of Sfax, University of Sfax, Sfax, Tunisia.
Chinmay Sundar RayDepartment of Ear, Nose, and Throat (ENT), Shrirama Chandra Bhanja (SCB) Medical College & Hospital, Cuttack, India.
Ashim DesaiDr. ABR Desai Ear, Nose and Throat (ENT) Clinic and Research Centre, Mumbai, India.
Khirod Chandra PandaDepartment of Ear, Nose, and Throat (ENT), Shrirama Chandra Bhanja (SCB) Medical College & Hospital, Cuttack, India.
Jyotish Chandra ChoudhuryDepartment of Forensic Medicine & Toxicology (FMT), Shrirama Chandra Bhanja (SCB) Medical College & Hospital, Cuttack, India.
Adel TekariLaboratory of Molecular and Cellular Screening Processes, Centre of Biotechnology of Sfax, University of Sfax, Sfax, Tunisia.
Saber MasmoudiLaboratory of Molecular and Cellular Screening Processes, Centre of Biotechnology of Sfax, University of Sfax, Sfax, Tunisia.
Puppala Venkat RamchanderInstitute of Life Sciences, Nalco Square, Chandrasekharpur, Bhubaneswar, India. pramchander@yahoo.com.ORCID http://orcid.org/0000-0003-2225-2252
Sriram Chandra Bhanja Medical College Hospital · INUniversity of Sfax · TNRegional Centre for Biotechnology · INInstitute of Life Sciences · IN

Funding

Department of Science and Technology, Ministry of Science and Technology (DST) DST/INT/TUNISIA/P-19/2017
6 · The paper itself

Abstract

Otosclerosis (OTSC) is a focal and diffuse bone disorder of the human middle ear characterized by abnormal bone growth and deposition at the stapes' footplate. This hinders the transmission of acoustic waves to the inner ear leading to subsequent conductive hearing loss. The plausible convections for the disease are genetic and environmental factors with yet an unraveled root cause. Recently, exome sequencing of European individuals with OTSC revealed rare pathogenic variants in the Serpin Peptidase Inhibitor, Clade F (SERPINF1) gene. Here, we sought to investigate the causal variants of SERPINF1 in the Indian population. The gene and protein expression was also evaluated in otosclerotic stapes to ameliorate our understanding of the potential effect of this gene in OTSC. A total of 230 OTSC patients and 230 healthy controls were genotyped by single-strand conformational polymorphism and Sanger sequencing methods. By comparing the case controls, we identified five rare variants (c.72 C > T, c.151 G > A, c.242 C > G, c.823 A > T, and c.826 T > A) only in patients. Four variants c.390 T > C (p = 0.048), c.440-39 C > T (p = 0.007), c.643 + 9 G > A (p = 0.035), and c.643 + 82 T > C (p = 0.005) were found to be significantly associated with the disease. Down-regulation of SERPINF1 transcript level in otosclerotic stapes was quantified by qRT-PCR, ddPCR and further validated by in situ hybridization. Similarly, reduced protein expression was observed by immunohistochemistry and immunofluorescence in otosclerotic stapes that corroborate with immunoblotting of patients' plasma samples. Our findings identified that SERPINF1 variants are associated with the disease. Furthermore, reduced expression of SERPINF1 in otosclerotic stapes might contribute to OTSC pathophysiology.

Indexed as

OtosclerosisDisease SusceptibilityGenotypeHumansPigment Epithelium-Derived FactorPolymerase Chain ReactionStapesPigment Epithelium-Derived Factor

Identifiers

PMID37308566
OpenAlexW4380324864

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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.