A new and fast method for diabetes and dyslipidemia diagnosis using FTIR-MIR, spectroscopy and multivariate data analysis: A proof of concept

Diabetes and dyslipidemia are well-established risk factors for cardiovascular disease, which is the primary cause of death both in Brazil and globally. Fourier-transform mid-infrared spectroscopy (FTIR-MIR) generates spectral fingerprints of biomolecules, allowing for correlation with metabolic cha...

Full description

Saved in:
Bibliographic Details
Published inChemometrics and intelligent laboratory systems Vol. 252; p. 105179
Main Authors Furman, Aline Emmer Ferreira, Cobre, Alexandre de Fátima, Stremel, Dile Pontarolo, Pontarolo, Roberto
Format Journal Article
LanguageEnglish
Published Elsevier B.V 15.09.2024
Subjects
Online AccessGet full text
ISSN0169-7439
DOI10.1016/j.chemolab.2024.105179

Cover

Loading…
More Information
Summary:Diabetes and dyslipidemia are well-established risk factors for cardiovascular disease, which is the primary cause of death both in Brazil and globally. Fourier-transform mid-infrared spectroscopy (FTIR-MIR) generates spectral fingerprints of biomolecules, allowing for correlation with metabolic changes, while remaining a rapid, non-invasive, and non-destructive method. The study provided a proof of concept for the effectiveness of FTIR-MIR in screening diabetes, pre-diabetes, hypercholesterolemia, hypertriglyceridemia, and mixed dyslipidemia in blood serum. After acquiring mid-infrared spectra of 60 human serum samples, both unsupervised and supervised analysis models were developed. Principal component analysis (PCA) was used for pattern recognition and to determine how closely related the samples were based on their spectral profiles. The results obtained by the supervised models showed a clear discriminative ability to distinguish both diabetic and dyslipidemic samples from healthy subjects by multivariate analysis performed on FTIR-MIR spectra. High accuracy rates of more than 90 % were achieved for diabetes and dyslipidemia diagnosis with PLS-DA. Dyslipidemia type discrimination could be attributed mainly to the amide I region [1720-1600 cm−1, (ν(CO)] and altered lipid concentration in the 3000-2800 cm−1 region, whereas the discrimination of diabetes and prediabetes was primarily due to the altered conformational protein in the Amides I [1720-1600 cm−1, ν(CO)] and Amide II [1570-1480 cm−1, δ(NH) + ν(CH)] range. •The multivariate analysis of FTIR-MIR discriminated between diabetes, pre-diabetes, and dyslipidemia in blood serum.•Unsupervised and supervised analysis models were developed using mid-infrared spectra from 60 samples.•PCA revealed the capacity to cluster samples based on their spectral profiles, effectively grouping them according to their diabetic and dyslipidemic status.•PLS-DA models achieved high accuracy rates of over 95% in diagnosing diabetes and 90% in diagnosing dyslipidemia types.
ISSN:0169-7439
DOI:10.1016/j.chemolab.2024.105179