Pulse Brain · Growing Health Evidence Index
Tier 2 — RCT, large cohort or strong causal designPeer-reviewed

Dihydroceramide- and ceramide-profiling provides insights into human cardiometabolic disease etiology

C. Wittenbecher; R. Cuadrat; L. Johnston; F. Eichelmann; S. Jäger; O. Kuxhaus; M. Prada; F. Del Greco M; A. Hicks; P. Hoffman; J. Krumsiek; Frank B. Hu; M. Schulze

Nature Communications · 2022

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Summary

This prospective cohort study in EPIC-Potsdam identified specific ceramide and dihydroceramide species that independently predict type 2 diabetes and cardiovascular disease risk, using a novel network-based approach. Mendelian randomisation supported a causal role for ceramide C22:0 in type 2 diabetes aetiology, and mediation analyses suggested these lipid metabolites link dietary habits (red meat consumption, coffee intake) and genetic predisposition to cardiometabolic disease risk.

Regional applicability

The study was conducted in Germany and may have limited direct applicability to UK populations, which differ in dietary patterns, genetic ancestry, and lifestyle factors. However, the mechanistic findings regarding ceramide biology and cardiometabolic disease pathways are likely relevant to understanding disease aetiology in UK populations, though UK-specific validation would be warranted.

Key measures

Plasma ceramide (C16:0, C18:0, C20:0, C22:0) and dihydroceramide (C20:0, C22:2, C26:1) concentrations; incidence of type 2 diabetes and cardiovascular disease; mediation analysis of dietary associations

Outcomes reported

The study identified specific ceramide and dihydroceramide species associated with prospective risk of type 2 diabetes and cardiovascular disease in a nested case-cohort design. It also examined whether these lipid metabolites mediate associations between dietary factors (red meat, coffee) and cardiometabolic disease risk.

Theme
Nutrition & health
Subject
Dietary fats & fatty acids
Study type
Research
Study design
Nested case-cohort with Mendelian randomisation and genome-wide association studies
Source type
Peer-reviewed study
Status
Published
Geography
Germany
System type
Human clinical
DOI
10.1038/s41467-022-28496-1
Catalogue ID
NRmu2qr5g4-05c

Topic tags

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