Non-invasive optical spectroscopic monitoring of breast development during puberty. Issue 1 (December 2017)

• Record Type: Journal Article
• Authors: Lilge, Lothar; Terry, Mary; Walter, Jane; Pinnaduwage, Dushanthi; Glendon, Gord; Hanna, Danielle; Tammemagi, Mai-Liis; Bradbury, Angela; Buys, Saundra; Daly, Mary; John, Esther; Knight, Julia; Andrulis, Irene
• Is Part Of: Breast cancer research. Volume 19:Issue 1(2017)
• Page Start: 1
• Page End: 8
• Publication Date: 2017-12
• Subjects: Optical spectroscopy -- Breast development -- Breast cancer family history -- Tanner staging -- LEGACY girls study; Breast -- Cancer -- Periodicals; 616.99449
• DOI: 10.1186/s13058-017-0805-x
• Languages: English
• ISSNs: 1465-542X

Abstract

Abstract Background Tanner staging (TS), a five-stage classification indicating no breast tissue (TS1) to full breast development (TS5), is used both in health research and clinical care to assess the onset of breast development (TS2) and duration in each stage. Currently, TS is measured both visually and through palpation but non-invasive methods will improve comparisons across settings. Methods We used optical spectroscopy (OS) measures from 102 girls at the Ontario site of the LEGACY girls study (average age 12 years, range 10.0–15.4 years) to determine whether breast tissue optical properties map to each TS. We further examined whether these properties differed by age, body mass index (BMI), and breast cancer risk score (BCRS) by examining the major principal components (PC). Results Age and BMI increased linearly with increasing TS. Eight PCs explained 99.9% of the variation in OS data. Unlike the linear increase with age and BMI, OS components had distinct patterns by TS: the onset of breast development (TS1 to TS2) was marked by elevation of PC3 scores indicating an increase in adipose tissue and decrease in signal from the pectoral muscle; transition to TS3 was marked by elevation of PC6 and PC7 and decline of PC2 scores indicating an increase in glandular or dense tissue; and transition to TS4+ by decline of PC2 scores representing a further increase in glandular tissue relative to adipose tissue. Of the eight PCs, three component scores (PC4, PC5, and PC8) remained in the best-fitting model of BCRS, suggesting different levels of collagen in the breast tissue by BCRS. Conclusions Our results suggest that serial measures of OS, a non-invasive assessment of breast tissue characteristics, can be used as an objective outcome that does not rely on visual inspection or palpation, for studying drivers of breast development.