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Biomedical Optics Express

Biomedical Optics Express

  • Editor: Joseph A. Izatt
  • Vol. 3, Iss. 9 — Sep. 1, 2012
  • pp: 2121–2130

The influence of frontal sinus in brain activation measurements by near-infrared spectroscopy analyzed by realistic head models

Kazuki Kurihara, Hiroshi Kawaguchi, Takayuki Obata, Hiroshi Ito, Kaoru Sakatani, and Eiji Okada  »View Author Affiliations


Biomedical Optics Express, Vol. 3, Issue 9, pp. 2121-2130 (2012)
http://dx.doi.org/10.1364/BOE.3.002121


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Abstract

Adequate modeling of light propagation in the head is important to predict the sensitivity of NIRS signal and the spatial sensitivity profile of source-detector pairs. The 3D realistic head models of which the geometry is based upon the anatomical images acquired by magnetic resonance imaging and x-ray computed tomography are constructed to investigate the influence of the frontal sinus on the NIRS signal and spatial sensitivity. Light propagation in the head is strongly affected by the presence of the frontal sinus. The light tends to propagate around the frontal sinus. The influence of the frontal sinus on the sensitivity of the NIRS signal to the brain activation is not consistent and depends on the depth of the frontal sinus, the optical properties of the superficial tissues and the relative position between the source-detector pair and the frontal sinus. The frontal sinus located in the shallow region of the skull tends to reduce the sensitivity of the NIRS signal while the deep frontal sinus can increase the sensitivity of the NIRS signal.

© 2012 OSA

OCIS Codes
(170.3660) Medical optics and biotechnology : Light propagation in tissues
(170.5280) Medical optics and biotechnology : Photon migration
(170.2655) Medical optics and biotechnology : Functional monitoring and imaging

ToC Category:
Optics of Tissue and Turbid Media

History
Original Manuscript: June 18, 2012
Revised Manuscript: July 29, 2012
Manuscript Accepted: July 29, 2012
Published: August 14, 2012

Virtual Issues
BIOMED 2012 (2012) Biomedical Optics Express

Citation
Kazuki Kurihara, Hiroshi Kawaguchi, Takayuki Obata, Hiroshi Ito, Kaoru Sakatani, and Eiji Okada, "The influence of frontal sinus in brain activation measurements by near-infrared spectroscopy analyzed by realistic head models," Biomed. Opt. Express 3, 2121-2130 (2012)
http://www.opticsinfobase.org/boe/abstract.cfm?URI=boe-3-9-2121


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References

  1. M. Ferrari and V. Quaresima, “A brief review on the history of human functional near-infrared spectroscopy (fNIRS) development and fields of application,” Neuroimage (to be published). [PubMed]
  2. H. Koizumi, T. Yamamoto, A. Maki, Y. Yamashita, H. Sato, H. Kawaguchi, and N. Ichikawa, “Optical topography: practical problems and new applications,” Appl. Opt.42(16), 3054–3062 (2003). [CrossRef] [PubMed]
  3. Y. Hoshi, B. H. Tsou, V. A. Billock, M. Tanosaki, Y. Iguchi, M. Shimada, T. Shinba, Y. Yamada, and I. Oda, “Spatiotemporal characteristics of hemodynamic changes in the human lateral prefrontal cortex during working memory tasks,” Neuroimage20(3), 1493–1504 (2003). [CrossRef] [PubMed]
  4. G. Taga and K. Asakawa, “Selectivity and localization of cortical response to auditory and visual stimulation in awake infants aged 2 to 4 months,” Neuroimage36(4), 1246–1252 (2007). [CrossRef] [PubMed]
  5. K. Uludağ, J. Steinbrink, M. Kohl-Bareis, R. Wenzel, A. Villringer, and H. Obrig, “Cytochrome-c-oxidase redox changes during visual stimulation measured by near-infrared spectroscopy cannot be explained by a mere cross talk artefact,” Neuroimage22(1), 109–119 (2004). [CrossRef] [PubMed]
  6. H. Wabnitz, M. Moeller, A. Liebert, H. Obrig, J. Steinbrink, and R. Macdonald, “Time-resolved near-infrared spectroscopy and imaging of the adult human brain,” Adv. Exp. Med. Biol.662, 143–148 (2010). [CrossRef] [PubMed]
  7. M. A. Franceschini, D. K. Joseph, T. J. Huppert, S. G. Diamond, and D. A. Boas, “Diffuse optical imaging of the whole head,” J. Biomed. Opt.11(5), 054007 (2006). [CrossRef] [PubMed]
  8. M. Wolf, M. Ferrari, and V. Quaresima, “Progress of near-infrared spectroscopy and topography for brain and muscle clinical applications,” J. Biomed. Opt.12(6), 062104 (2007). [CrossRef] [PubMed]
  9. K. Sakatani, Y. Murata, N. Fujiwara, T. Hoshino, S. Nakamura, T. Kano, and Y. Katayama, “Comparison of blood-oxygen-level-dependent functional magnetic resonance imaging and near-infrared spectroscopy recording during functional brain activation in patients with stroke and brain tumors,” J. Biomed. Opt.12(6), 062110 (2007). [CrossRef] [PubMed]
  10. S. Muehlschlegel, J. Selb, M. Patel, S. G. Diamond, M. A. Franceschini, A. G. Sorensen, D. A. Boas, and L. H. Schwamm, “Feasibility of NIRS in the neurointensive care unit: a pilot study in stroke using physiological oscillations,” Neurocrit. Care11(2), 288–295 (2009). [CrossRef] [PubMed]
  11. T. Suto, M. Fukuda, M. Ito, T. Uehara, and M. Mikuni, “Multichannel near-infrared spectroscopy in depression and schizophrenia: cognitive brain activation study,” Biol. Psychiatry55(5), 501–511 (2004). [CrossRef] [PubMed]
  12. I. Miyai, H. C. Tanabe, I. Sase, H. Eda, I. Oda, I. Konishi, Y. Tsunazawa, T. Suzuki, T. Yanagida, and K. Kubota, “Cortical mapping of gait in humans: a near-infrared spectroscopic topography study,” Neuroimage14(5), 1186–1192 (2001). [CrossRef] [PubMed]
  13. E. Watanabe, A. Maki, F. Kawaguchi, K. Takashiro, Y. Yamashita, H. Koizumi, and Y. Mayanagi, “Non-invasive assessment of language dominance with near-infrared spectroscopic mapping,” Neurosci. Lett.256(1), 49–52 (1998). [CrossRef] [PubMed]
  14. E. Okada, M. Firbank, M. Schweiger, S. R. Arridge, M. Cope, and D. T. Delpy, “Theoretical and experimental investigation of near-infrared light propagation in a model of the adult head,” Appl. Opt.36(1), 21–31 (1997). [CrossRef] [PubMed]
  15. M. Wolf, M. Keel, V. Dietz, K. von Siebenthal, H. U. Bucher, and O. Baenziger, “The influence of a clear layer on near-infrared spectrophotometry measurements using a liquid neonatal head phantom,” Phys. Med. Biol.44(7), 1743–1753 (1999). [CrossRef] [PubMed]
  16. E. Okada and D. T. Delpy, “Near-infrared light propagation in an adult head model. I. Modeling of low-level scattering in the cerebrospinal fluid layer,” Appl. Opt.42(16), 2906–2914 (2003). [CrossRef] [PubMed]
  17. D. A. Boas, J. P. Culver, J. J. Stott, and A. K. Dunn, “Three dimensional Monte Carlo code for photon migration through complex heterogeneous media including the adult human head,” Opt. Express10(3), 159–170 (2002). [PubMed]
  18. Y. Fukui, Y. Ajichi, and E. Okada, “Monte Carlo prediction of near-infrared light propagation in realistic adult and neonatal head models,” Appl. Opt.42(16), 2881–2887 (2003). [CrossRef] [PubMed]
  19. H. Kawaguchi, T. Koyama, and E. Okada, “Effect of probe arrangement on reproducibility of images by near-infrared topography evaluated by a virtual head phantom,” Appl. Opt.46(10), 1658–1668 (2007). [CrossRef] [PubMed]
  20. J. Heiskala, P. Hiltunen, and I. Nissilä, “Significance of background optical properties, time-resolved information and optode arrangement in diffuse optical imaging of term neonates,” Phys. Med. Biol.54(3), 535–554 (2009). [CrossRef] [PubMed]
  21. M. Dehaes, L. Gagnon, F. Lesage, M. Pélégrini-Issac, A. Vignaud, R. Valabrègue, R. Grebe, F. Wallois, and H. Benali, “Quantitative investigation of the effect of the extra-cerebral vasculature in diffuse optical imaging: a simulation study,” Biomed. Opt. Express2(3), 680–695 (2011). [CrossRef] [PubMed]
  22. E. Okada, D. Yamamoto, N. Kiryu, A. Katagiri, N. Yokose, T. Awano, K. Igarashi, S. Nakamura, T. Hoshino, Y. Murata, T. Kano, K. Sakatani, and Y. Katayama, “Theoretical and experimental investigation of the influence of frontal sinus on the sensitivity of the NIRS signal in the adult head,” Adv. Exp. Med. Biol.662, 231–236 (2010). [CrossRef] [PubMed]
  23. J. Ashburner, “A fast diffeomorphic image registration algorithm,” Neuroimage38(1), 95–113 (2007). [CrossRef] [PubMed]
  24. J. Thiran, V. Warscotte, and B. Macq, “A queue-based region growing algorithm for accurate segmentation of multi-dimensional digital images,” Signal Process.60(1), 1–10 (1997). [CrossRef]
  25. C. R. Simpson, M. Kohl, M. Essenpreis, and M. Cope, “Near-infrared optical properties of ex vivo human skin and subcutaneous tissues measured using the Monte Carlo inversion technique,” Phys. Med. Biol.43(9), 2465–2478 (1998). [CrossRef] [PubMed]
  26. M. Firbank, M. Hiraoka, M. Essenpreis, and D. T. Delpy, “Measurement of the optical properties of the skull in the wavelength range 650-950 nm,” Phys. Med. Biol.38(4), 503–510 (1993). [CrossRef] [PubMed]
  27. P. van der Zee, M. Essenpreis, and D. T. Delpy, “Optical properties of brain tissue,” Proc. SPIE1888, 454–465 (1993). [CrossRef]
  28. A. Roggan, O. Minet, C. Shröder, and G. Müller, “The determination of optical tissue properties with double integrating sphere technique and Monte Carlo simulation,” Proc. SPIE2100, 42–56 (1994). [CrossRef]
  29. A. N. Yaroslavsky, P. C. Schulze, I. V. Yaroslavsky, R. Schober, F. Ulrich, and H.-J. Schwarzmaier, “Optical properties of selected native and coagulated human brain tissues in vitro in the visible and near infrared spectral range,” Phys. Med. Biol.47(12), 2059–2073 (2002). [CrossRef] [PubMed]
  30. B. C. Wilson and G. Adam, “A Monte Carlo model for the absorption and flux distributions of light in tissue,” Med. Phys.10(6), 824–830 (1983). [CrossRef] [PubMed]
  31. M. Hiraoka, M. Firbank, M. Essenpreis, M. Cope, S. R. Arridge, P. van der Zee, and D. T. Delpy, “A Monte Carlo investigation of optical pathlength in inhomogeneous tissue and its application to near-infrared spectroscopy,” Phys. Med. Biol.38(12), 1859–1876 (1993). [CrossRef] [PubMed]
  32. L. Wang, S. L. Jacques, and L. Zheng, “MCML—Monte Carlo modeling of light transport in multi-layered tissues,” Comput. Methods Programs Biomed.47(2), 131–146 (1995). [CrossRef]

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