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Quantitative physiology of the precancerous cervix in vivo through optical spectroscopy.

Publication ,  Journal Article
Chang, VT-C; Cartwright, PS; Bean, SM; Palmer, GM; Bentley, RC; Ramanujam, N
Published in: Neoplasia
April 2009

Cervical cancer is the second most common female cancer worldwide. The ability to quantify physiological and morphological changes in the cervix is not only useful in the diagnosis of cervical precancers but also important in aiding the design of cost-effective detection systems for use in developing countries that lack well-established screening and diagnostic programs. We assessed the capability of a diffuse reflectance spectroscopy technique to identify contrasts in optical biomarkers that vary with different grades of cervical intraepithelial neoplasia (CIN) from normal cervical tissues. The technology consists of an optical probe and an instrument (with broadband light source, dispersive element, and detector), and a Monte Carlo algorithm to extract optical biomarker contributions including total hemoglobin (Hb) concentration, Hb saturation, and reduced scattering coefficient from the measured spectra. Among 38 patients and 89 sites examined, 46 squamous normal sites, 18 CIN 1, and 15 CIN 2(+) sites were included in the analysis. Total Hb was statistically higher in CIN 2(+) (18.3 +/- 3.6 microM, mean +/- SE) compared with normal (9.58 +/- 1.91 microM) and CIN 1 (12.8 +/- 2.6 microM), whereas scattering was significantly reduced in CIN 1 (8.3 +/- 0.8 cm(-1)) and CIN 2(+) (8.6 +/- 1.0 cm(-1)) compared with normal (10.2 +/- 1.1 cm(-1)). Hemoglobin saturation was not significantly altered in CIN 2(+) compared with normal and CIN 1. The difference in total Hb is likely because of stromal angiogenesis, whereas decreased scattering can be attributed to breakdown of collagen network in the cervical stroma.

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Published In

Neoplasia

DOI

EISSN

1476-5586

Publication Date

April 2009

Volume

11

Issue

4

Start / End Page

325 / 332

Location

United States

Related Subject Headings

  • Uterine Cervical Neoplasms
  • Uterine Cervical Dysplasia
  • Spectrum Analysis
  • Precancerous Conditions
  • Oncology & Carcinogenesis
  • Monte Carlo Method
  • Humans
  • Hemoglobins
  • Fiber Optic Technology
  • Female
 

Citation

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Chang, V.-C., Cartwright, P. S., Bean, S. M., Palmer, G. M., Bentley, R. C., & Ramanujam, N. (2009). Quantitative physiology of the precancerous cervix in vivo through optical spectroscopy. Neoplasia, 11(4), 325–332. https://doi.org/10.1593/neo.81386
Chang, Vivide Tuan-Chyan, Peter S. Cartwright, Sarah M. Bean, Greg M. Palmer, Rex C. Bentley, and Nirmala Ramanujam. “Quantitative physiology of the precancerous cervix in vivo through optical spectroscopy.Neoplasia 11, no. 4 (April 2009): 325–32. https://doi.org/10.1593/neo.81386.
Chang VT-C, Cartwright PS, Bean SM, Palmer GM, Bentley RC, Ramanujam N. Quantitative physiology of the precancerous cervix in vivo through optical spectroscopy. Neoplasia. 2009 Apr;11(4):325–32.
Chang, Vivide Tuan-Chyan, et al. “Quantitative physiology of the precancerous cervix in vivo through optical spectroscopy.Neoplasia, vol. 11, no. 4, Apr. 2009, pp. 325–32. Pubmed, doi:10.1593/neo.81386.
Chang VT-C, Cartwright PS, Bean SM, Palmer GM, Bentley RC, Ramanujam N. Quantitative physiology of the precancerous cervix in vivo through optical spectroscopy. Neoplasia. 2009 Apr;11(4):325–332.
Journal cover image

Published In

Neoplasia

DOI

EISSN

1476-5586

Publication Date

April 2009

Volume

11

Issue

4

Start / End Page

325 / 332

Location

United States

Related Subject Headings

  • Uterine Cervical Neoplasms
  • Uterine Cervical Dysplasia
  • Spectrum Analysis
  • Precancerous Conditions
  • Oncology & Carcinogenesis
  • Monte Carlo Method
  • Humans
  • Hemoglobins
  • Fiber Optic Technology
  • Female