Evidence map›Paper›PMID 21895336›Full record

ArticleJournal of biomedical optics2011

Wavelength selection-based nonlinear calibration for transcutaneous blood glucose sensing using Raman spectroscopy.

Narahara Chari Dingari, Ishan Barman, Jeon Woong Kang, Chae-Ryon Kong, Ramachandra R Dasari, Michael S Feld

Abstract read
In one paragraph

Article in Journal of biomedical optics, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing 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

16 citing papers in PubMed.

  1. Article
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  4. Tissue Phantoms for Biomedical Applications in Raman Spectroscopy: A Review.Biomedical engineering and computational biology · 2020
    Review
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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

6 authors.

Narahara Chari DingariMassachusetts Institute of Technology, G. R. Harrison Spectroscopy Laboratory, Laser Biomedical Research Center, Cambridge, Massachusetts 02139, USA.
Ishan Barman
Jeon Woong Kang
Chae-Ryon Kong
Ramachandra R Dasari
Michael S Feld

Funding

WIDE-FIELD REFLECTION PHASE MICROSCOPYP41RR002594 · NCRR · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI PARK, YOUNGKYU · 1985 to 2011
$12.3M
NCRR NIH HHS P41 RR002594NCRR NIH HHS P41-RR02594
6 · The paper itself

Abstract

While Raman spectroscopy provides a powerful tool for noninvasive and real time diagnostics of biological samples, its translation to the clinical setting has been impeded by the lack of robustness of spectroscopic calibration models and the size and cumbersome nature of conventional laboratory Raman systems. Linear multivariate calibration models employing full spectrum analysis are often misled by spurious correlations, such as system drift and covariations among constituents. In addition, such calibration schemes are prone to overfitting, especially in the presence of external interferences that may create nonlinearities in the spectra-concentration relationship. To address both of these issues we incorporate residue error plot-based wavelength selection and nonlinear support vector regression (SVR). Wavelength selection is used to eliminate uninformative regions of the spectrum, while SVR is used to model the curved effects such as those created by tissue turbidity and temperature fluctuations. Using glucose detection in tissue phantoms as a representative example, we show that even a substantial reduction in the number of wavelengths analyzed using SVR lead to calibration models of equivalent prediction accuracy as linear full spectrum analysis. Further, with clinical datasets obtained from human subject studies, we also demonstrate the prospective applicability of the selected wavelength subsets without sacrificing prediction accuracy, which has extensive implications for calibration maintenance and transfer. Additionally, such wavelength selection could substantially reduce the collection time of serial Raman acquisition systems. Given the reduced footprint of serial Raman systems in relation to conventional dispersive Raman spectrometers, we anticipate that the incorporation of wavelength selection in such hardware designs will enhance the possibility of miniaturized clinical systems for disease diagnosis in the near future.

Indexed as

Signal Processing, Computer-AssistedBlood Chemical AnalysisBlood GlucoseHumansLeast-Squares AnalysisPhantoms, ImagingSpectrum Analysis, RamanSupport Vector MachineBlood Glucose

Identifiers

PMID21895336
PMCPMC3162621

What OpenQuestion holds

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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.