Evidence map›Paper›PMID 38580818›Full record

ReviewMolecular biology reports2024

The advent of RNA-based therapeutics for metabolic syndrome and associated conditions: a comprehensive review of the literature.

Helen Ye Rim Huang, Sarah Badar, Mohammad Said, Siddiqah Shah, Hareesha Rishab Bharadwaj, Krishna Ramamoorthy, Maen Monketh Alrawashdeh, Faaraea Haroon, Jawad Basit, Sajeel Saeed and 4 more

Abstract readReview
PubMed Publisher
In one paragraph

Review in Molecular biology reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. 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

14 authors.

Helen Ye Rim HuangFaculty of Medicine and Health Science, Royal College of Surgeons in Ireland, Dublin, Ireland.
Sarah BadarDepartment of Biomedical Science, The University of the West Scotland, Paisley, Scotland.
Mohammad SaidFaculty of Medicine and Health Science, Royal College of Surgeons in Ireland, Dublin, Ireland.
Siddiqah ShahFaculty of Medicine and Health Science, Royal College of Surgeons in Ireland, Dublin, Ireland.
Hareesha Rishab BharadwajFaculty of Biology Medicine and Health, The University of Manchester, Manchester, UK.
Krishna RamamoorthyDepartment of Biochemistry and Microbiology, Rutgers University-New Brunswick, Brunswick, NJ, USA.
Maen Monketh AlrawashdehFaculty of Medicine and Health Science, Royal College of Surgeons in Ireland, Dublin, Ireland.
Faaraea HaroonHealth Services Academy, Islamabad, Pakistan.
Jawad BasitRawalpindi Medical University, Rawalpindi, Pakistan.
Sajeel SaeedRawalpindi Medical University, Rawalpindi, Pakistan.
Narjiss AjiFaculty of Medicine and Health, McGill University, Montreal, QC, Canada.
Gary TseTianjin Key Laboratory of Ionic-Molecular Function of Cardiovascular Disease, Department of Cardiology, Tianjin Institute of Cardiology, Second Hospital of Tianjin Medical University, Tianjin, China.
Priyanka RoyDirectorate of Factories, Department of Labour, Government of West Bengal, Kolkata, India.
Mainak BardhanMiami Cancer Institute, Baptist Health South Florida, Miami, FL, USA. bardhan.mainak@gmail.com.ORCID http://orcid.org/0000-0002-4106-409X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Metabolic syndrome (MetS) is a prevalent and intricate health condition affecting a significant global population, characterized by a cluster of metabolic and hormonal disorders disrupting lipid and glucose metabolism pathways. Clinical manifestations encompass obesity, dyslipidemia, insulin resistance, and hypertension, contributing to heightened risks of diabetes and cardiovascular diseases. Existing medications often fall short in addressing the syndrome's multifaceted nature, leading to suboptimal treatment outcomes and potential long-term health risks. This scenario underscores the pressing need for innovative therapeutic approaches in MetS management. RNA-based treatments, employing small interfering RNAs (siRNAs), microRNAs (miRNAs), and antisense oligonucleotides (ASOs), emerge as promising strategies to target underlying biological abnormalities. However, a summary of research available on the role of RNA-based therapeutics in MetS and related co-morbidities is limited. Murine models and human studies have been separately interrogated to determine whether there have been recent advancements in RNA-based therapeutics to offer a comprehensive understanding of treatment available for MetS. In a narrative fashion, we searched for relevant articles pertaining to MetS co-morbidities such as cardiovascular disease, fatty liver disease, dementia, colorectal cancer, and endocrine abnormalities. We emphasize the urgency of exploring novel therapeutic avenues to address the intricate pathophysiology of MetS and underscore the potential of RNA-based treatments, coupled with advanced delivery systems, as a transformative approach for achieving more comprehensive and efficacious outcomes in MetS patients.

Indexed as

Cardiovascular DiseasesHypertensionInsulin ResistanceMetabolic SyndromeMicroRNAsAnimalsHumansMiceObesityRNA, Small InterferingMicroRNAsRNA, Small InterferingInsulin resistanceLipid metabolismMetabolic syndromeRNA therapeutics

Identifiers

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.