Evidence map›Paper›PMID 39729198›Full record

ArticleMetabolic brain disease2024

Causal relationship between dyslipidemia and diabetic neuropathy: a mendelian randomization study.

Cong Li, Yu Feng, Lina Feng, Mingquan Li

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Article in Metabolic brain disease, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

4 authors.

Cong LiCollege of Traditional Chinese Medicine, Changchun University of Chinese Medicine, Changchun, China.
Yu FengAffiliated Hospital of the Changchun University of Chinese Medicine, Changchun, China.
Lina FengDepartment of Neurology, the Second Affiliated Hospital of Shandong First Medical University, Shandong First Medical University & Shandong Academy of Medical Sciences, Taian, 271000, China. fenglina0001@163.com.ORCID 0000-0003-0504-5390
Mingquan LiDepartment of Neurology, Third Affiliated Clinical Hospital of the Changchun University of Chinese Medicine, Changchun, 130022, China. limingquan0001@126.com.ORCID 0000-0001-7717-1711

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Some studies have shown an association between dyslipidemia and diabetic neuropathy (DN), but the genetic association has not been clarified. Therefore, the present study aimed to investigate the genetic causal association between dyslipidemia and DN through a Mendelian randomization (MR) approach. Genetic causal associations between total cholesterol (TC), triglyceride (TG), low-density lipoprotein cholesterol (LDL), and high-density lipoprotein cholesterol (HDL) and DN were investigated by MR to provide a basis for the prevention and treatment of DN. Significant and independent single-nucleotide polymorphisms (SNPs) identified in genome-wide association studies were selected as instrumental variables (IVs) for MR analysis. Inverse variance weighted (IVW), MR‒Egger regression, weighted median (WME), simple mode (SM), and weighted mode (WM) methods were used to analyze causal associations. Heterogeneity and multiplicity tests were also performed and analyzed using the leave-one-out method to assess the stability of the results. Genetically predicted TC and DN (OR = 0.793, 95% CI = 0.655⁓0.961, P = 0.019) and LDL and DN (OR = 0.842, 95% CI = 0.711⁓0.998, P = 0.049) may be causally associated, but no causal associations were found between TG and DN (OR = 0.837, 95% CI = 0.631⁓1.111, P = 0.221) or between HDL and DN (OR = 1.192, 95% CI = 0.940⁓1.510, P = 0.149). TC and LDL may have genetic causal associations with DN, though no genetic causal associations were found for TG or HDL with DN. However, this study may have several limitations, and further clinical studies are needed to expand the sample size for future validation.

Indexed as

Diabetic NeuropathiesDyslipidemiasGenome-Wide Association StudyMendelian Randomization AnalysisPolymorphism, Single NucleotideCholesterol, HDLCholesterol, LDLHumansTriglyceridesCholesterol, HDLCholesterol, LDLTriglyceridesCausal association analysisDiabetic neuropathyDyslipidemiaMendelian randomization

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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.