Abstract
The V measure captures grayscale intensity variation on a mammogram and is positively associated with breast cancer risk, independent of percent mammographic density (PMD), an established marker of breast cancer risk. We examined whether anthropometrics are associated with V, independent of PMD.
The analysis included 1,700 premenopausal and 1,947 postmenopausal women without breast cancer within the Nurses' Health Study (NHS) and NHSII. Participants recalled their body fatness at ages 5, 10, and 20 years using a 9-level pictogram (level 1: most lean) and reported weight at age 18 years, current adult weight, and adult height. V was estimated by calculating standard deviation of pixels on screening mammograms. Linear mixed models were used to estimate beta coefficients (ß) and 95% confidence intervals (CI) for the relationships between anthropometric measures and V, adjusting for confounders and PMD.
V and PMD were positively correlated (Spearman r = 0.60). Higher average body fatness at ages 5 to 10 years (level ≥ 4.5 vs. 1) was significantly associated with lower V in premenopausal (ß = −0.32; 95% CI, −0.48 to −0.16) and postmenopausal (ß = −0.24; 95% CI, −0.37 to −0.10) women, independent of current body mass index (BMI) and PMD. Similar inverse associations were observed with average body fatness at ages 10 to 20 years and BMI at age 18 years. Current BMI was inversely associated with V, but the associations were largely attenuated after adjustment for PMD. Height was not associated with V.
Our data suggest that early-life body fatness may reflect lifelong impact on breast tissue architecture beyond breast density. However, further studies are needed to confirm the results.
This study highlights strong inverse associations of early-life adiposity with mammographic image intensity variation.
Introduction
Anthropometrics such as height (1–3) and body fatness (3–11) are associated with breast cancer risk. Height is thought to indicate early-life nutritional status (12) and correlates with timing of puberty and early-life exposure to endogenous growth hormones. A meta-analysis of 159 prospective cohorts estimated a 17% elevated breast cancer risk associated with every 10-cm increase in adult height (2). Higher childhood and adolescent body fatness and young adult body mass index (BMI) are consistently inversely associated with both pre- and postmenopausal breast cancer risk (4–8, 13), whereas later adult body fatness is positively associated with postmenopausal breast cancer risk (3, 9–11). Although the mechanisms underlying the relationships between anthropometrics and breast cancer risk are unknown, one of the hypothesized mechanisms is that exposure, particularly during childhood and adolescence, may influence development of breast tissue structures and determine breast density. Percent mammographic density (PMD) is a strong breast cancer risk factor, which has been associated with 4- to 6-fold higher risk of breast cancer (14–16).
Multiple studies of PMD, which refers to the relative amount of dense (fibroglandular) versus nondense (adipose) tissue in the breast, have reported associations with early-life and adult anthropometrics (17–22). However, other features within a mammogram may provide additional information beyond PMD. Recently, novel algorithms have been developed to measure the heterogeneity in patterns of mammographic density, the features referred to as “texture.” Independent studies from the United States (23, 24) and the UK (25) have shown that various measures of texture features, ranging from simple distribution of grayscale intensity values to the spatial relationships between intensities on a mammogram, are associated with breast cancer risk, independent of PMD. In the Nurses' Health Study (NHS) and NHSII, we quantified the V metric, a measure of texture that captures variation in grayscale intensity values on a mammogram, using automated techniques. Using these data, we previously found that higher V, indicating greater intensity variation, was associated with a 41% increased breast cancer risk in premenopausal women and a 21% increased risk in postmenopausal women, after adjustment for PMD (24). These studies have provided evidence that, even among women with similar PMD, texture features such as V can further differentiate and predict women who are at increased risk of developing breast cancer later in life.
However, little is known about the factors associated with the V. Investigating the associations of established breast cancer risk factors with V may provide new insights into the mechanisms through which these risk factors influence breast cancer risk. Using automated techniques, we examined the associations of early-life and adult anthropometrics (childhood and adolescent body fatness, BMI at age 18, current adult BMI, change in BMI since age 18, predicted body fat mass, predicted percent body fat, and adult height) with V among pre- and postmenopausal women in the NHS and the NHSII.
Materials and Methods
Study population
The NHS began in 1976 among 121,700 female registered nurses at ages 30 to 55 years. The NHSII began in 1989 among 116,429 female registered nurses at ages 25 to 42 years. In both cohorts, baseline and subsequent biennial follow-up questionnaires were used to collect information on participants' health behaviors, anthropometric and lifestyle factors, reproductive factors, medical histories, and disease diagnosis (26).
This analysis includes participants who served as controls in a nested case–control study of breast cancer within the NHS and NHSII blood and cheek cell collection subcohorts. Details of this nested case–control study have been previously described (27–29). In brief, blood samples were collected from 32,826 NHS participants ages 43 to 70 years in 1989 to 1990 and 29,611 NHSII participants ages 32 to 45 years in 1996 to 1999. Up to two controls were matched to incident breast cancer cases on age, menopausal status at blood draw and diagnosis, current postmenopausal hormone therapy use, month, time of day, fasting status at time of blood collection, and luteal day (NHSII timed samples only). From the cases and controls, mammograms imaged as close as possible to the date of blood draw (or 1997 for cheek cell collection subcohort) were collected (NHS: 1,379 cases and 2,514 controls; NHSII: 758 cases and 1,832 controls).
For this analysis, we restricted to controls and excluded women with missing information on V or PMD (n = 338), anthropometrics (childhood and adolescent body fatness, BMI at age 18 years, current adult BMI, adult height; n = 291), and menopausal status (n = 70). A total of 3,647 women (1,700 premenopausal and 1,947 postmenopausal) were included in this analysis. The study protocol was approved by the institutional review boards of the Brigham and Women's Hospital and Harvard T.H. Chan School of Public Health, and those of participating registries as required.
Exposure assessment
Body fatness at ages 5, 10, and 20 years were recalled in 1988 (NHS) and 1989 (NHSII) using Stunkard's nine-level pictogram (levels 1 to 9: most lean to most overweight; ref. 30). Recalled body fatness using this pictogram by women at ages 71 to 76 years has shown a good correlation with measured BMI at ages 5 to 20 (Pearson r = 0.60 to 0.66; ref. 31). Average body fatness at ages 5 and 10 years and ages 10 and 20 years were used to represent childhood and adolescent body fatness, respectively. Extreme levels (≥4.5) were collapsed into a single category because there were fewer women in those levels. Height and weight at age 18 were reported via the baseline questionnaire (in 1976 for NHS and 1989 for NHSII). Current weight was reported via questionnaires administered prior to but around the time of mammogram. BMI (kg/m2) was calculated by dividing weight (kg) by baseline height (m) squared. Change in BMI since age 18 (kg/m2) was estimated by subtracting BMI at age 18 from current adult BMI. To account for limitations of BMI as a measure of adiposity, we also calculated predicted body fat mass (kg) and percent fat mass on the basis of age, race, height, weight, and waist circumference using the equations developed and validated in the National Health and Nutrition Examination Survey (32). The analyses of predicted body fat mass and percent fat mass were restricted to 1,078 premenopausal and 1,464 postmenopausal women with information on waist circumference. All continuous exposure variables (BMI at age 18, current adult BMI, change in BMI since age 18, predicted body fat mass, predicted percent body fat, and adult height) were categorized based on quintiles.
Mammographic density measurement
Details of mammographic density measurement were described elsewhere (33). Briefly, a Lumysis 85 laser film scanner was used to digitize the craniocaudal views of both breasts for all mammograms in the NHS and for the first two batches of mammograms in the NHSII. The third batch of mammograms in the NHSII was scanned using a VIDAR CAD PRO Advantage scanner (VIDAR Systems Corporation) using comparable resolution of 150 dots per inch and 12 bit depth. We measured absolute dense area and total area using the Cumulus software for computer-assisted thresholding (34). PMD was estimated by dividing the dense area by the total area and then averaged that of both breasts. All images were read by a single observer (within person intraclass correlation >0.90). We adjusted for batch variability in the NHSII as previously described (33).
Mammographic texture variation measurement (“the V metric”)
The V metric is an automated measure that captures mammographic image intensity, as described previously (35, 36). Briefly, the breast area is detected and eroded [by 25% (“V75”) and 35% (“V65”) along a radial direction] to eliminate the proportion of the breast that was not in contact with the compression paddle during the image acquisition, which is an approximation. The standard deviation calculated from pixels within the eroded breast region produces V. Images were digitized with different equipment and were from various time frames. To account for resolution and intensity scale differences, mammograms were normalized before V was calculated (24). Normalization processing involved spatial normalization, feature distribution normalization, and resolution estimation (Supplementary Methods and Materials). Example images of breasts with high versus low V values given similar PMD are shown in Fig. 1.
Statistical analysis
Because mammographic density and texture measures varied by menopausal status, all analyses were stratified by menopausal status at time of mammogram. To account for correlations among the controls within the matched sets, we performed linear mixed models with a compound symmetry correlation structure to estimate beta coefficients (ß) and 95% confidence intervals (CI) for the relationships between anthropometrics and V. Multivariable (MV) models included age, race, personal history of benign breast disease, family history of breast cancer, parity/age at first birth, alcohol use, smoking, and breastfeeding. In postmenopausal women, age at menopause and postmenopausal hormone use were additionally adjusted. For change in BMI since age 18, models additionally adjusted for BMI at age 18. For all analyses, we used covariate information reported via questionnaires assessed prior to but around the time of mammogram. We performed tests for trend using the median of the exposure categories as a continuous variable in the regression models. To evaluate whether the associations between anthropometrics and V are driven by their correlations with other mammographic measures, we compared the models after additional adjustment for PMD, dense area, and nondense area, separately. For early-life anthropometrics, we also evaluated the role of potential mediators by comparing the models with and without adjustment for BMI at age 18 and current adult BMI. Additional adjustment for age at menarche did not change the results and thus are not shown in this paper. To assess whether the associations vary by the levels of PMD, we stratified analyses by low versus high PMD (below vs. above the menopausal-specific median PMD) and performed tests for interaction using a Wald test for interaction terms. We also examined the relationships with PMD, absolute dense area, and absolute nondense area by performing models on square-root transformed density measures, adjusting for V. In primary analyses, we used the data from V75 breast erosion strategy and low resolution images. In sensitivity analyses, we repeated the analyses using an alternate breast erosion strategy (V65) and after restricting to data from high-resolution images (n = 1,242 premenopausal, 850 postmenopausal). We also stratified by digitization methods to account for measurement differences in V by these methods.
Results
Participant characteristics
The mean age at mammogram was 45.9 years in 1,700 premenopausal women and 58.0 years in 1,947 postmenopausal women. Most women were white (97%) and parous (89%). On average, women with greater average body fatness at ages 5 to 10 years (level ≥4.5 vs. 1) were less likely to be non-white (1.4% vs. 4.9%) and have personal history of benign breast disease (14% vs. 22%) and more likely to have higher BMI at age 18 (23.8 vs. 19.6 kg/m2), higher current adult BMI (28.7 vs. 24.2 kg/m2), and younger age at menarche (11.9 vs. 12.8 years; Table 1). Women with greater average body fatness at ages 5 to 10 years were also more likely to have lower PMD and absolute dense area and higher absolute nondense area.
. | Childhood body fatness (average at ages 5–10 years) . | ||||
---|---|---|---|---|---|
. | Level 1 . | Level 1.5–2 . | Level 2.5–3 . | Level 3.5–4 . | Level ≥4.5 . |
. | (N = 835) . | (N = 1,063) . | (N = 851) . | (N = 565) . | (N = 333) . |
Mean (SD) or percentage | |||||
Age at mammograma, years | 55.0 (9.1) | 51.8 (8.9) | 51.1 (8.6) | 51.7 (8.4) | 51.9 (8.4) |
Nonwhite, % | 4.9 | 3.2 | 4.4 | 2.4 | 1.4 |
Height, inches | 64.7 (2.4) | 64.8 (2.4) | 64.8 (2.5) | 64.7 (2.4) | 64.7 (2.5) |
BMI at age 18 years, kg/m2 | 19.6 (2.0) | 20.4 (2.2) | 21.5 (2.6) | 22.8 (3.0) | 23.8 (3.2) |
BMI at mammogramb, kg/m2 | 24.2 (4.1) | 25.0 (4.7) | 26.3 (5.3) | 27.9 (6.2) | 28.7 (6.3) |
Predicted body fat mass at mammogramb, kg | 24.3 (7.0) | 25.7 (7.9) | 27.4 (9.0) | 30.4 (10.4) | 31.1 (9.7) |
Predicted percent body fat mass at mammogramb | 36.8 (3.9) | 37.5 (4.3) | 38.3 (4.7) | 40.0 (5.6) | 40.4 (5.2) |
Age at menarche, years | 12.8 (1.4) | 12.5 (1.4) | 12.4 (1.4) | 12.2 (1.4) | 11.9 (1.3) |
Parousb, % | 88.5 | 88.8 | 90.5 | 88.1 | 85.9 |
Among parous womenb | |||||
Parityb,c | 2.8 (1.3) | 2.8 (1.3) | 2.7 (1.3) | 2.8 (1.3) | 2.8 (1.3) |
Age at first birthb,c, years | 25.5 (3.6) | 25.5 (3.9) | 25.7 (4.0) | 25.4 (3.8) | 25.5 (4.0) |
Total breastfeedingb,c, % | |||||
<1 month | 35.7 | 32.3 | 31.5 | 32.8 | 28.3 |
1–6 months | 22.0 | 18.7 | 20.0 | 17.8 | 22.0 |
7–12 months | 14.3 | 13.4 | 12.6 | 13.9 | 18.6 |
≥13 months | 28.0 | 35.6 | 35.8 | 35.5 | 31.0 |
Postmenopausalb, % | 53.2 | 54.7 | 52.5 | 53.6 | 53.8 |
Among postmenopausal womenb | |||||
Postmenopausal hormone useb,d | |||||
Never users | 33.7 | 31.4 | 38.8 | 34.9 | 41.3 |
Former users | 19.8 | 18.8 | 18.1 | 19.9 | 19.8 |
Current users | 46.5 | 49.8 | 43.0 | 45.2 | 38.9 |
Age at menopauseb,d, years | 45.2 (6.6) | 44.9 (7.5) | 46.1 (6.8) | 45.2 (7.2) | 45.4 (7.4) |
Alcohol intakeb, g/d | |||||
0 | 32.2 | 33.0 | 35.8 | 35.4 | 35.4 |
0.1–4.9 | 33.0 | 34.7 | 32.4 | 30.2 | 34.6 |
5.0–14.9 | 19.2 | 19.7 | 19.8 | 20.8 | 16.3 |
≥15.0 | 8.4 | 7.0 | 6.6 | 7.7 | 8.3 |
Missing | 7.3 | 5.6 | 5.5 | 5.9 | 5.3 |
Smokingb, % | |||||
Never | 56.9 | 60.8 | 57.5 | 56.1 | 51.1 |
Former | 33.5 | 31.6 | 34.1 | 35.5 | 37.3 |
Current | 9.6 | 7.5 | 8.4 | 8.4 | 11.6 |
Personal history of benign breast diseaseb, % | 21.9 | 21.2 | 19.1 | 19.4 | 14.0 |
Family history of breast cancerb, % | 11.0 | 11.1 | 9.4 | 11.3 | 7.4 |
Percent mammographic densityb | 35.9 (19.4) | 35.8 (19.2) | 31.0 (19.6) | 27.8 (19.1) | 23.6 (18.7) |
Absolute dense areab, cm2 | 43.3 (26.8) | 43.7 (27.9) | 40.1 (27.6) | 38.8 (28.5) | 32.9 (26.6) |
Absolute nondense areab, cm2 | 91.5 (61.8) | 93.8 (64.9) | 111.8 (78.8) | 124.8 (77.8) | 135.7 (78.4) |
V measures | 0.12 (0.91) | 0.09 (0.95) | −0.12 (0.98) | −0.27 (1.00) | −0.58 (0.90) |
. | Childhood body fatness (average at ages 5–10 years) . | ||||
---|---|---|---|---|---|
. | Level 1 . | Level 1.5–2 . | Level 2.5–3 . | Level 3.5–4 . | Level ≥4.5 . |
. | (N = 835) . | (N = 1,063) . | (N = 851) . | (N = 565) . | (N = 333) . |
Mean (SD) or percentage | |||||
Age at mammograma, years | 55.0 (9.1) | 51.8 (8.9) | 51.1 (8.6) | 51.7 (8.4) | 51.9 (8.4) |
Nonwhite, % | 4.9 | 3.2 | 4.4 | 2.4 | 1.4 |
Height, inches | 64.7 (2.4) | 64.8 (2.4) | 64.8 (2.5) | 64.7 (2.4) | 64.7 (2.5) |
BMI at age 18 years, kg/m2 | 19.6 (2.0) | 20.4 (2.2) | 21.5 (2.6) | 22.8 (3.0) | 23.8 (3.2) |
BMI at mammogramb, kg/m2 | 24.2 (4.1) | 25.0 (4.7) | 26.3 (5.3) | 27.9 (6.2) | 28.7 (6.3) |
Predicted body fat mass at mammogramb, kg | 24.3 (7.0) | 25.7 (7.9) | 27.4 (9.0) | 30.4 (10.4) | 31.1 (9.7) |
Predicted percent body fat mass at mammogramb | 36.8 (3.9) | 37.5 (4.3) | 38.3 (4.7) | 40.0 (5.6) | 40.4 (5.2) |
Age at menarche, years | 12.8 (1.4) | 12.5 (1.4) | 12.4 (1.4) | 12.2 (1.4) | 11.9 (1.3) |
Parousb, % | 88.5 | 88.8 | 90.5 | 88.1 | 85.9 |
Among parous womenb | |||||
Parityb,c | 2.8 (1.3) | 2.8 (1.3) | 2.7 (1.3) | 2.8 (1.3) | 2.8 (1.3) |
Age at first birthb,c, years | 25.5 (3.6) | 25.5 (3.9) | 25.7 (4.0) | 25.4 (3.8) | 25.5 (4.0) |
Total breastfeedingb,c, % | |||||
<1 month | 35.7 | 32.3 | 31.5 | 32.8 | 28.3 |
1–6 months | 22.0 | 18.7 | 20.0 | 17.8 | 22.0 |
7–12 months | 14.3 | 13.4 | 12.6 | 13.9 | 18.6 |
≥13 months | 28.0 | 35.6 | 35.8 | 35.5 | 31.0 |
Postmenopausalb, % | 53.2 | 54.7 | 52.5 | 53.6 | 53.8 |
Among postmenopausal womenb | |||||
Postmenopausal hormone useb,d | |||||
Never users | 33.7 | 31.4 | 38.8 | 34.9 | 41.3 |
Former users | 19.8 | 18.8 | 18.1 | 19.9 | 19.8 |
Current users | 46.5 | 49.8 | 43.0 | 45.2 | 38.9 |
Age at menopauseb,d, years | 45.2 (6.6) | 44.9 (7.5) | 46.1 (6.8) | 45.2 (7.2) | 45.4 (7.4) |
Alcohol intakeb, g/d | |||||
0 | 32.2 | 33.0 | 35.8 | 35.4 | 35.4 |
0.1–4.9 | 33.0 | 34.7 | 32.4 | 30.2 | 34.6 |
5.0–14.9 | 19.2 | 19.7 | 19.8 | 20.8 | 16.3 |
≥15.0 | 8.4 | 7.0 | 6.6 | 7.7 | 8.3 |
Missing | 7.3 | 5.6 | 5.5 | 5.9 | 5.3 |
Smokingb, % | |||||
Never | 56.9 | 60.8 | 57.5 | 56.1 | 51.1 |
Former | 33.5 | 31.6 | 34.1 | 35.5 | 37.3 |
Current | 9.6 | 7.5 | 8.4 | 8.4 | 11.6 |
Personal history of benign breast diseaseb, % | 21.9 | 21.2 | 19.1 | 19.4 | 14.0 |
Family history of breast cancerb, % | 11.0 | 11.1 | 9.4 | 11.3 | 7.4 |
Percent mammographic densityb | 35.9 (19.4) | 35.8 (19.2) | 31.0 (19.6) | 27.8 (19.1) | 23.6 (18.7) |
Absolute dense areab, cm2 | 43.3 (26.8) | 43.7 (27.9) | 40.1 (27.6) | 38.8 (28.5) | 32.9 (26.6) |
Absolute nondense areab, cm2 | 91.5 (61.8) | 93.8 (64.9) | 111.8 (78.8) | 124.8 (77.8) | 135.7 (78.4) |
V measures | 0.12 (0.91) | 0.09 (0.95) | −0.12 (0.98) | −0.27 (1.00) | −0.58 (0.90) |
Note: Values are means (SD) or percentages, standardized to the age distribution of the study population, except for age. Values of polytomous variables may not sum to 100% due to rounding. V measures = V75 erosion, low resolution; V measures can take negative values because of the mapping.
aValue is not age adjusted.
bAt the time of mammogram.
cAmong parous women only.
dAmong postmenopausal women only.
Compared with postmenopausal women, premenopausal women had higher V (mean = 0.15 vs. −0.26), PMD (mean = 39.5% vs. 26.0%), and absolute dense area (mean = 45.7 vs. 37.4 cm2) and lower absolute nondense area (mean = 80.6 vs. 128.3 cm2). Among both pre- and postmenopausal women, V was positively correlated with PMD (Spearman r = 0.49 in premenopausal, 0.63 in postmenopausal) and absolute dense area (Spearman r = 0.39 in premenopausal, 0.48 in postmenopausal) but negatively correlated with absolute nondense area (Spearman r = −0.38 in premenopausal, −0.53 in postmenopausal) within a mammogram.
Early-life body fatness
Greater childhood body fatness (level ≥4.5 vs. 1) was statistically significantly associated with lower V in multivariable models among both premenopausal (β = −0.74; 95% CI, −0.92 to −0.57, P trend < 0.01) and postmenopausal women (β = −0.59; 95% CI, −0.75 to −0.43, P trend < 0.01; Table 2). After additional adjustment for current BMI and PMD, the associations were substantially attenuated but remained statistically significant (premenopausal: β = −0.32; 95% CI, −0.48 to −0.16; postmenopausal: β = −0.24; 95% CI, −0.37 to −0.10; P trends < 0.01). Similar inverse associations were observed for adolescent body fatness (level ≥4.5 vs. 1: β = −0.41; 95% CI, −0.64 to −0.18 in premenopausal; β = −0.34; 95% CI, −0.50 to −0.18 in postmenopausal) and BMI at age 18 years (≥23 vs. <19 kg/m2: β = −0.30; 95% CI, −0.45 to −0.16 in premenopausal; β = −0.25; 95% CI, −0.37 to −0.14 in postmenopausal) in multivariable models including current BMI and PMD (all P trend < 0.01). The associations between early-life body fatness and V were only slightly attenuated when absolute dense or nondense area was included in the models instead of PMD (all P trend < 0.01).
. | Beta coefficients (95% CIs) . | |||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|
. | Premenopausal women (N = 1,700) . | Postmenopausal women (N = 1,947) . | ||||||||||
. | N . | MV-adjusteda . | MV + current BMIb . | MV + current BMI + PMDc . | N . | MV-adjusteda . | MV + current BMIb . | MV + current BMI + PMDc . | ||||
Childhood body fatness (average at ages 5–10 years) | ||||||||||||
Level 1 | 303 | 0 (Ref) | 0 (Ref) | 0 (Ref) | 532 | 0 (Ref) | 0 (Ref) | 0 (Ref) | ||||
Level 1.5–2 | 507 | −0.09 (−0.22, 0.04) | −0.03 (−0.16, 0.10) | −0.04 (−0.16, 0.07) | 556 | 0.03 (−0.08, 0.14) | 0.05 (−0.06, 0.15) | 0.004 (−0.09, 0.10) | ||||
Level 2.5–3 | 454 | −0.20 (−0.33, −0.06) | −0.07 (−0.20, 0.06) | −0.04 (−0.16, 0.08) | 397 | −0.25 (−0.37, −0.13) | −0.17 (−0.28, −0.05) | −0.11 (−0.21, −0.01) | ||||
Level 3.5–4 | 275 | −0.45 (−0.60, −0.30) | −0.23 (−0.38, −0.08) | −0.12 (−0.26, 0.01) | 290 | −0.31 (−0.45, −0.18) | −0.17 (−0.30, −0.04) | −0.11 (−0.22, 0.001) | ||||
Level ≥4.5 | 161 | −0.74 (−0.92, −0.57) | −0.46 (−0.63, −0.28) | −0.32 (−0.48, −0.16) | 172 | −0.59 (−0.75, −0.43) | −0.43 (−0.58, −0.27) | −0.24 (−0.37, −0.10) | ||||
P trend | <0.01 | <0.01 | <0.01 | <0.01 | <0.01 | <0.01 | ||||||
Adolescent body fatness (average at ages 10–20 years) | ||||||||||||
Level 1 | 72 | 0 (Ref) | 0 (Ref) | 0 (Ref) | 173 | 0 (Ref) | 0 (Ref) | 0 (Ref) | ||||
Level 1.5–2 | 427 | −0.06 (−0.29, 0.17) | −0.03 (−0.25, 0.19) | −0.05 (−0.25, 0.15) | 585 | −0.09 (−0.25, 0.07) | −0.06 (−0.21, 0.09) | −0.10 (−0.23, 0.03) | ||||
Level 2.5–3 | 608 | −0.20 (−0.42, 0.02) | −0.09 (−0.30, 0.13) | −0.07 (−0.27, 0.13) | 614 | −0.20 (−0.35, −0.04) | −0.11 (−0.26, 0.04) | −0.12 (−0.25, 0.01) | ||||
Level 3.5–4 | 405 | −0.49 (−0.72, −0.27) | −0.28 (−0.51, −0.06) | −0.19 (−0.39, 0.02) | 358 | −0.43 (−0.59, −0.26) | −0.29 (−0.46, −0.13) | −0.25 (−0.39, −0.11) | ||||
Level ≥4.5 | 188 | −0.95 (−1.20, −0.70) | −0.58 (−0.83, −0.33) | −0.41 (−0.64, −0.18) | 217 | −0.79 (−0.97, −0.60) | −0.53 (−0.71, −0.35) | −0.34 (−0.50, −0.18) | ||||
P trend | <0.01 | <0.01 | <0.01 | <0.01 | <0.01 | <0.01 | ||||||
BMI at age 18 years, kg/m2 | ||||||||||||
<19.0 | 342 | 0 (Ref) | 0 (Ref) | 0 (Ref) | 382 | 0 (Ref) | 0 (Ref) | 0 (Ref) | ||||
19.0–19.9 | 308 | −0.15 (−0.29, −0.01) | −0.10 (−0.23, 0.04) | −0.09 (−0.21, 0.04) | 313 | −0.12 (−0.25, 0.02) | −0.08 (−0.21, 0.06) | −0.13 (−0.25, −0.02) | ||||
20.0–20.9 | 315 | −0.14 (−0.28, −0.002) | −0.03 (−0.16, 0.11) | 0.004 (−0.12, 0.13) | 368 | −0.17 (−0.30, −0.03) | −0.08 (−0.21, 0.04) | −0.10 (−0.21, 0.01) | ||||
21.0–22.9 | 411 | −0.36 (−0.49, −0.24) | −0.19 (−0.32, −0.06) | −0.12 (−0.24, 0.003) | 478 | −0.31 (−0.43, −0.19) | −0.15 (−0.27, −0.03) | −0.14 (−0.25, −0.03) | ||||
≥23.0 | 324 | −0.84 (−0.98, −0.70) | −0.47 (−0.63, −0.32) | −0.30 (−0.45, −0.16) | 406 | −0.70 (−0.82, −0.57) | −0.42 (−0.56, −0.29) | −0.25 (−0.37, −0.14) | ||||
P trend | <0.01 | <0.01 | <0.01 | <0.01 | <0.01 | <0.01 | ||||||
Per 1-kg/m2 increase | −0.13 (−0.14, −0.11) | −0.07 (−0.09, −0.05) | −0.04 (−0.06, −0.02) | −0.10 (−0.12, −0.09) | −0.06 (−0.08, −0.04) | −0.03 (−0.05, −0.02) |
. | Beta coefficients (95% CIs) . | |||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|
. | Premenopausal women (N = 1,700) . | Postmenopausal women (N = 1,947) . | ||||||||||
. | N . | MV-adjusteda . | MV + current BMIb . | MV + current BMI + PMDc . | N . | MV-adjusteda . | MV + current BMIb . | MV + current BMI + PMDc . | ||||
Childhood body fatness (average at ages 5–10 years) | ||||||||||||
Level 1 | 303 | 0 (Ref) | 0 (Ref) | 0 (Ref) | 532 | 0 (Ref) | 0 (Ref) | 0 (Ref) | ||||
Level 1.5–2 | 507 | −0.09 (−0.22, 0.04) | −0.03 (−0.16, 0.10) | −0.04 (−0.16, 0.07) | 556 | 0.03 (−0.08, 0.14) | 0.05 (−0.06, 0.15) | 0.004 (−0.09, 0.10) | ||||
Level 2.5–3 | 454 | −0.20 (−0.33, −0.06) | −0.07 (−0.20, 0.06) | −0.04 (−0.16, 0.08) | 397 | −0.25 (−0.37, −0.13) | −0.17 (−0.28, −0.05) | −0.11 (−0.21, −0.01) | ||||
Level 3.5–4 | 275 | −0.45 (−0.60, −0.30) | −0.23 (−0.38, −0.08) | −0.12 (−0.26, 0.01) | 290 | −0.31 (−0.45, −0.18) | −0.17 (−0.30, −0.04) | −0.11 (−0.22, 0.001) | ||||
Level ≥4.5 | 161 | −0.74 (−0.92, −0.57) | −0.46 (−0.63, −0.28) | −0.32 (−0.48, −0.16) | 172 | −0.59 (−0.75, −0.43) | −0.43 (−0.58, −0.27) | −0.24 (−0.37, −0.10) | ||||
P trend | <0.01 | <0.01 | <0.01 | <0.01 | <0.01 | <0.01 | ||||||
Adolescent body fatness (average at ages 10–20 years) | ||||||||||||
Level 1 | 72 | 0 (Ref) | 0 (Ref) | 0 (Ref) | 173 | 0 (Ref) | 0 (Ref) | 0 (Ref) | ||||
Level 1.5–2 | 427 | −0.06 (−0.29, 0.17) | −0.03 (−0.25, 0.19) | −0.05 (−0.25, 0.15) | 585 | −0.09 (−0.25, 0.07) | −0.06 (−0.21, 0.09) | −0.10 (−0.23, 0.03) | ||||
Level 2.5–3 | 608 | −0.20 (−0.42, 0.02) | −0.09 (−0.30, 0.13) | −0.07 (−0.27, 0.13) | 614 | −0.20 (−0.35, −0.04) | −0.11 (−0.26, 0.04) | −0.12 (−0.25, 0.01) | ||||
Level 3.5–4 | 405 | −0.49 (−0.72, −0.27) | −0.28 (−0.51, −0.06) | −0.19 (−0.39, 0.02) | 358 | −0.43 (−0.59, −0.26) | −0.29 (−0.46, −0.13) | −0.25 (−0.39, −0.11) | ||||
Level ≥4.5 | 188 | −0.95 (−1.20, −0.70) | −0.58 (−0.83, −0.33) | −0.41 (−0.64, −0.18) | 217 | −0.79 (−0.97, −0.60) | −0.53 (−0.71, −0.35) | −0.34 (−0.50, −0.18) | ||||
P trend | <0.01 | <0.01 | <0.01 | <0.01 | <0.01 | <0.01 | ||||||
BMI at age 18 years, kg/m2 | ||||||||||||
<19.0 | 342 | 0 (Ref) | 0 (Ref) | 0 (Ref) | 382 | 0 (Ref) | 0 (Ref) | 0 (Ref) | ||||
19.0–19.9 | 308 | −0.15 (−0.29, −0.01) | −0.10 (−0.23, 0.04) | −0.09 (−0.21, 0.04) | 313 | −0.12 (−0.25, 0.02) | −0.08 (−0.21, 0.06) | −0.13 (−0.25, −0.02) | ||||
20.0–20.9 | 315 | −0.14 (−0.28, −0.002) | −0.03 (−0.16, 0.11) | 0.004 (−0.12, 0.13) | 368 | −0.17 (−0.30, −0.03) | −0.08 (−0.21, 0.04) | −0.10 (−0.21, 0.01) | ||||
21.0–22.9 | 411 | −0.36 (−0.49, −0.24) | −0.19 (−0.32, −0.06) | −0.12 (−0.24, 0.003) | 478 | −0.31 (−0.43, −0.19) | −0.15 (−0.27, −0.03) | −0.14 (−0.25, −0.03) | ||||
≥23.0 | 324 | −0.84 (−0.98, −0.70) | −0.47 (−0.63, −0.32) | −0.30 (−0.45, −0.16) | 406 | −0.70 (−0.82, −0.57) | −0.42 (−0.56, −0.29) | −0.25 (−0.37, −0.14) | ||||
P trend | <0.01 | <0.01 | <0.01 | <0.01 | <0.01 | <0.01 | ||||||
Per 1-kg/m2 increase | −0.13 (−0.14, −0.11) | −0.07 (−0.09, −0.05) | −0.04 (−0.06, −0.02) | −0.10 (−0.12, −0.09) | −0.06 (−0.08, −0.04) | −0.03 (−0.05, −0.02) |
Note: V metric = V75 erosion, low resolution.
aMV-adjusted model includes age (years, continuous), race (white/nonwhite), personal history of benign breast disease (yes/no), family history of breast cancer (yes/no), parity/age at first birth (nulliparous, 1–2 births/<25 years, 1–2 births/25–29 years, 1–2 births/≥30 years, ≥3 births/<25 years, ≥3 births/≥25 years, parous/missing age at first birth), alcohol use (0, 0.1–4.9, 5.0–14.9, ≥15 g/d, missing), smoking (never, former, current), breastfeeding (<1, 1–6, 7–12, ≥13 months), and, in postmenopausal women, age at menopause (≤44, 45–49, 50–54, ≥55 years, missing) and postmenopausal hormone use (never, former, current).
bAdditionally includes current BMI (kg/m2, continuous) in the MV-adjusted model.
cAdditionally includes current BMI (kg/m2, continuous) and percent mammographic density (square-root transformed, continuous) in the MV-adjusted model.
Current adult body fatness
In pre- and postmenopausal women, current adult BMI (≥30 vs. <21 kg/m2) was significantly inversely associated with V, adjusting for childhood body fatness and potential confounders (premenopausal: β = −0.74; 95% CI, −0.89 to −0.59; postmenopausal: β = −0.74; 95% CI, −0.88 to −0.59; all P-trend < 0.01) (Table 3). The associations were substantially attenuated after additional adjustment for PMD (premenopausal: β = −0.12; 95% CI, −0.27 to 0.03; postmenopausal: β = −0.08; 95% CI, −0.22 to 0.05); however, the inverse trend remained statistically significant. Similar patterns were observed when adjusted for absolute nondense area instead of PMD. Adjustment for absolute dense area only slightly attenuated the associations. Similar results were observed with change in BMI since age 18 (>7 vs. ≤0 kg/m2: β = −0.03; 95% CI, −0.18 to 0.12 in premenopausal; β = −0.04; 95% CI, −0.17 to 0.09 in postmenopausal), predicted body fat mass (≥35 vs. <20 kg: β = −0.05; 95% CI, −0.23 to 0.13 in premenopausal; β = −0.12; 95% CI, −0.26 to 0.03 in postmenopausal), and percent body fat mass (≥43% vs. <35%: β = −0.19; 95% CI, −0.38 to 0.001 in premenopausal; β = −0.10; 95% CI, −0.24 to 0.05 in postmenopausal) in multivariable models including childhood body fatness and PMD.
. | Beta coefficients (95% CIs) . | |||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|
. | Premenopausal women (N = 1,700) . | Postmenopausal women (N = 1,947) . | ||||||||||
. | N . | MV-adjusteda . | MV + childhood body fatnessb . | MV + childhood body fatness + PMDc . | N . | MV-adjusteda . | MV + childhood body fatnessb . | MV + childhood body fatness + PMDc . | ||||
Current adult BMI, kg/m2 | ||||||||||||
<21.0 | 285 | 0 (Ref) | 0 (Ref) | 0 (Ref) | 243 | 0 (Ref) | 0 (Ref) | 0 (Ref) | ||||
21.0–22.9 | 351 | 0.08 (−0.06, 0.22) | 0.08 (−0.05, 0.22) | 0.21 (0.09, 0.34) | 335 | −0.05 (−0.20, 0.09) | −0.03 (−0.18, 0.12) | 0.11 (−0.02, 0.24) | ||||
23.0–24.9 | 329 | 0.03 (−0.11, 0.17) | 0.07 (−0.07, 0.21) | 0.30 (0.17, 0.43) | 390 | −0.20 (−0.34, −0.06) | −0.17 (−0.31, −0.02) | 0.08 (−0.05, 0.20) | ||||
25.0–29.9 | 429 | −0.29 (−0.43, −0.16) | −0.25 (−0.38, −0.11) | 0.14 (0.01, 0.27) | 601 | −0.48 (−0.61, −0.34) | −0.43 (−0.56, −0.29) | −0.01 (−0.13, 0.11) | ||||
≥30.0 | 306 | −0.85 (−1.00, −0.71) | −0.74 (−0.89, −0.59) | −0.12 (−0.27, 0.03) | 378 | −0.83 (−0.97, −0.68) | −0.74 (−0.88, −0.59) | −0.08 (−0.22, 0.05) | ||||
P trend | <0.01 | <0.01 | <0.01 | <0.01 | <0.01 | 0.01 | ||||||
Per 1-kg/m2 increase | −0.07 (−0.08, −0.06) | −0.06 (−0.07, −0.05) | −0.02 (−0.03, −0.01) | −0.07 (−0.08, −0.06) | −0.06 (−0.07, −0.05) | −0.01 (−0.02, −0.003) | ||||||
Change in BMI since age 18 years, kg/m2 | ||||||||||||
≤0 | 0 (Ref) | 0 (Ref) | 0 (Ref) | 206 | 0 (Ref) | 0 (Ref) | 0 (Ref) | |||||
0.1–2.0 | 193 | −0.10 (−0.26, 0.06) | −0.09 (−0.25, 0.08) | −0.01 (−0.15, 0.14) | 291 | −0.05 (−0.21, 0.11) | −0.05 (−0.21, 0.11) | 0.02 (−0.11, 0.16) | ||||
2.1–5.0 | 326 | −0.07 (−0.22, 0.08) | −0.07 (−0.22, 0.09) | 0.14 (−0.002, 0.28) | 618 | −0.10 (−0.24, 0.05) | −0.11 (−0.25, 0.04) | 0.10 (−0.02, 0.23) | ||||
5.1–7.0 | 560 | −0.28 (−0.45, −0.11) | −0.27 (−0.44, −0.10) | 0.11 (−0.05, 0.27) | 300 | −0.19 (−0.36, −0.03) | −0.20 (−0.36, −0.04) | 0.10 (−0.04, 0.25) | ||||
>7.0 | 239 | −0.46 (−0.62, −0.31) | −0.45 (−0.60, −0.29) | −0.03 (−0.18, 0.12) | 532 | −0.52 (−0.67, −0.37) | −0.52 (−0.67, −0.37) | −0.04 (−0.17, 0.09) | ||||
P trend | 382 | <0.01 | <0.01 | 0.47 | <0.01 | <0.01 | 0.09 | |||||
Per 1-kg/m2 increase | −0.05 (−0.06, −0.03) | −0.04 (−0.06, −0.03) | −0.004 (−0.02, 0.01) | −0.05 (−0.06, −0.03) | −0.05 (−0.06, −0.04) | −0.01 (−0.02, 0.001) | ||||||
Premenopausal women (N = 1,078)d | Postmenopausal women (N = 1,464)d | |||||||||||
Predicted body fat mass, kg | ||||||||||||
<20.0 | 272 | 0 (Ref) | 0 (Ref) | 0 (Ref) | 250 | 0 (Ref) | 0 (Ref) | 0 (Ref) | ||||
20.0–24.9 | 331 | 0.15 (0.0001, 0.29) | 0.17 (0.02, 0.31) | 0.32 (0.19, 0.45) | 427 | −0.11 (−0.25, 0.03) | −0.10 (−0.24, 0.05) | 0.05 (−0.07, 0.18) | ||||
25.0–29.9 | 201 | −0.21 (−0.37, −0.04) | −0.15 (−0.31, 0.02) | 0.16 (0.01, 0.32) | 342 | −0.32 (−0.47, −0.17) | −0.29 (−0.44, −0.14) | 0.003 (−0.13, 0.13) | ||||
30.0–34.9 | 115 | −0.39 (−0.59, −0.19) | −0.32 (−0.51, −0.12) | 0.08 (−0.11, 0.26) | 197 | −0.57 (−0.74, −0.40) | −0.52 (−0.69, −0.35) | −0.12 (−0.27, 0.03) | ||||
≥35.0 | 159 | −0.75 (−0.93, −0.57) | −0.64 (−0.82, −0.45) | −0.05 (−0.23, 0.13) | 248 | −0.83 (−0.99, −0.67) | −0.75 (−0.91, −0.58) | −0.12 (−0.26, 0.03) | ||||
P trend | <0.01 | <0.01 | 0.06 | <0.01 | <0.01 | 0.01 | ||||||
Per 1-kg increase | −0.03 (−0.04, −0.03) | −0.03 (−0.04, −0.02) | −0.01 (−0.01, 0.0004) | −0.04 (−0.04, −0.03) | −0.03 (−0.04, −0.03) | −0.01 (−0.01, −0.001) | ||||||
Predicted percent body fat mass | ||||||||||||
<35.0 | 397 | 0 (Ref) | 0 (Ref) | 0 (Ref) | 299 | 0 (Ref) | 0 (Ref) | 0 (Ref) | ||||
35.0–36.9 | 234 | 0.13 (−0.02, 0.27) | 0.15 (0.01, 0.29) | 0.29 (0.15, 0.42) | 317 | −0.04 (−0.19, 0.10) | −0.02 (−0.17, 0.12) | 0.14 (0.02, 0.26) | ||||
37.0–39.9 | 207 | −0.38 (−0.53, −0.23) | −0.34 (−0.49, −0.19) | 0.03 (−0.12, 0.18) | 363 | −0.25 (−0.39, −0.11) | −0.22 (−0.36, −0.08) | 0.07 (−0.05, 0.20) | ||||
40.0–42.9 | 117 | −0.45 (−0.64, −0.27) | −0.38 (−0.57, −0.20) | −0.01 (−0.18, 0.17) | 233 | −0.57 (−0.73, −0.41) | −0.52 (−0.68, −0.36) | −0.06 (−0.20, 0.08) | ||||
≥43.0 | 123 | −0.92 (−1.10, −0.73) | −0.80 (−0.99, −0.61) | −0.19 (−0.38, 0.001) | 252 | −0.83 (−0.99, −0.67) | −0.75 (−0.91, −0.59) | −0.10 (−0.24, 0.05) | ||||
P trend | <0.01 | <0.01 | 0.02 | <0.01 | <0.01 | 0.01 | ||||||
Per 1% increase | −0.07 (−0.08, −0.06) | −0.06 (−0.07, −0.05) | −0.02 (−0.03, −0.002) | −0.07 (−0.08, −0.06) | −0.06 (−0.07, −0.05) | −0.01 (−0.02, −0.003) |
. | Beta coefficients (95% CIs) . | |||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|
. | Premenopausal women (N = 1,700) . | Postmenopausal women (N = 1,947) . | ||||||||||
. | N . | MV-adjusteda . | MV + childhood body fatnessb . | MV + childhood body fatness + PMDc . | N . | MV-adjusteda . | MV + childhood body fatnessb . | MV + childhood body fatness + PMDc . | ||||
Current adult BMI, kg/m2 | ||||||||||||
<21.0 | 285 | 0 (Ref) | 0 (Ref) | 0 (Ref) | 243 | 0 (Ref) | 0 (Ref) | 0 (Ref) | ||||
21.0–22.9 | 351 | 0.08 (−0.06, 0.22) | 0.08 (−0.05, 0.22) | 0.21 (0.09, 0.34) | 335 | −0.05 (−0.20, 0.09) | −0.03 (−0.18, 0.12) | 0.11 (−0.02, 0.24) | ||||
23.0–24.9 | 329 | 0.03 (−0.11, 0.17) | 0.07 (−0.07, 0.21) | 0.30 (0.17, 0.43) | 390 | −0.20 (−0.34, −0.06) | −0.17 (−0.31, −0.02) | 0.08 (−0.05, 0.20) | ||||
25.0–29.9 | 429 | −0.29 (−0.43, −0.16) | −0.25 (−0.38, −0.11) | 0.14 (0.01, 0.27) | 601 | −0.48 (−0.61, −0.34) | −0.43 (−0.56, −0.29) | −0.01 (−0.13, 0.11) | ||||
≥30.0 | 306 | −0.85 (−1.00, −0.71) | −0.74 (−0.89, −0.59) | −0.12 (−0.27, 0.03) | 378 | −0.83 (−0.97, −0.68) | −0.74 (−0.88, −0.59) | −0.08 (−0.22, 0.05) | ||||
P trend | <0.01 | <0.01 | <0.01 | <0.01 | <0.01 | 0.01 | ||||||
Per 1-kg/m2 increase | −0.07 (−0.08, −0.06) | −0.06 (−0.07, −0.05) | −0.02 (−0.03, −0.01) | −0.07 (−0.08, −0.06) | −0.06 (−0.07, −0.05) | −0.01 (−0.02, −0.003) | ||||||
Change in BMI since age 18 years, kg/m2 | ||||||||||||
≤0 | 0 (Ref) | 0 (Ref) | 0 (Ref) | 206 | 0 (Ref) | 0 (Ref) | 0 (Ref) | |||||
0.1–2.0 | 193 | −0.10 (−0.26, 0.06) | −0.09 (−0.25, 0.08) | −0.01 (−0.15, 0.14) | 291 | −0.05 (−0.21, 0.11) | −0.05 (−0.21, 0.11) | 0.02 (−0.11, 0.16) | ||||
2.1–5.0 | 326 | −0.07 (−0.22, 0.08) | −0.07 (−0.22, 0.09) | 0.14 (−0.002, 0.28) | 618 | −0.10 (−0.24, 0.05) | −0.11 (−0.25, 0.04) | 0.10 (−0.02, 0.23) | ||||
5.1–7.0 | 560 | −0.28 (−0.45, −0.11) | −0.27 (−0.44, −0.10) | 0.11 (−0.05, 0.27) | 300 | −0.19 (−0.36, −0.03) | −0.20 (−0.36, −0.04) | 0.10 (−0.04, 0.25) | ||||
>7.0 | 239 | −0.46 (−0.62, −0.31) | −0.45 (−0.60, −0.29) | −0.03 (−0.18, 0.12) | 532 | −0.52 (−0.67, −0.37) | −0.52 (−0.67, −0.37) | −0.04 (−0.17, 0.09) | ||||
P trend | 382 | <0.01 | <0.01 | 0.47 | <0.01 | <0.01 | 0.09 | |||||
Per 1-kg/m2 increase | −0.05 (−0.06, −0.03) | −0.04 (−0.06, −0.03) | −0.004 (−0.02, 0.01) | −0.05 (−0.06, −0.03) | −0.05 (−0.06, −0.04) | −0.01 (−0.02, 0.001) | ||||||
Premenopausal women (N = 1,078)d | Postmenopausal women (N = 1,464)d | |||||||||||
Predicted body fat mass, kg | ||||||||||||
<20.0 | 272 | 0 (Ref) | 0 (Ref) | 0 (Ref) | 250 | 0 (Ref) | 0 (Ref) | 0 (Ref) | ||||
20.0–24.9 | 331 | 0.15 (0.0001, 0.29) | 0.17 (0.02, 0.31) | 0.32 (0.19, 0.45) | 427 | −0.11 (−0.25, 0.03) | −0.10 (−0.24, 0.05) | 0.05 (−0.07, 0.18) | ||||
25.0–29.9 | 201 | −0.21 (−0.37, −0.04) | −0.15 (−0.31, 0.02) | 0.16 (0.01, 0.32) | 342 | −0.32 (−0.47, −0.17) | −0.29 (−0.44, −0.14) | 0.003 (−0.13, 0.13) | ||||
30.0–34.9 | 115 | −0.39 (−0.59, −0.19) | −0.32 (−0.51, −0.12) | 0.08 (−0.11, 0.26) | 197 | −0.57 (−0.74, −0.40) | −0.52 (−0.69, −0.35) | −0.12 (−0.27, 0.03) | ||||
≥35.0 | 159 | −0.75 (−0.93, −0.57) | −0.64 (−0.82, −0.45) | −0.05 (−0.23, 0.13) | 248 | −0.83 (−0.99, −0.67) | −0.75 (−0.91, −0.58) | −0.12 (−0.26, 0.03) | ||||
P trend | <0.01 | <0.01 | 0.06 | <0.01 | <0.01 | 0.01 | ||||||
Per 1-kg increase | −0.03 (−0.04, −0.03) | −0.03 (−0.04, −0.02) | −0.01 (−0.01, 0.0004) | −0.04 (−0.04, −0.03) | −0.03 (−0.04, −0.03) | −0.01 (−0.01, −0.001) | ||||||
Predicted percent body fat mass | ||||||||||||
<35.0 | 397 | 0 (Ref) | 0 (Ref) | 0 (Ref) | 299 | 0 (Ref) | 0 (Ref) | 0 (Ref) | ||||
35.0–36.9 | 234 | 0.13 (−0.02, 0.27) | 0.15 (0.01, 0.29) | 0.29 (0.15, 0.42) | 317 | −0.04 (−0.19, 0.10) | −0.02 (−0.17, 0.12) | 0.14 (0.02, 0.26) | ||||
37.0–39.9 | 207 | −0.38 (−0.53, −0.23) | −0.34 (−0.49, −0.19) | 0.03 (−0.12, 0.18) | 363 | −0.25 (−0.39, −0.11) | −0.22 (−0.36, −0.08) | 0.07 (−0.05, 0.20) | ||||
40.0–42.9 | 117 | −0.45 (−0.64, −0.27) | −0.38 (−0.57, −0.20) | −0.01 (−0.18, 0.17) | 233 | −0.57 (−0.73, −0.41) | −0.52 (−0.68, −0.36) | −0.06 (−0.20, 0.08) | ||||
≥43.0 | 123 | −0.92 (−1.10, −0.73) | −0.80 (−0.99, −0.61) | −0.19 (−0.38, 0.001) | 252 | −0.83 (−0.99, −0.67) | −0.75 (−0.91, −0.59) | −0.10 (−0.24, 0.05) | ||||
P trend | <0.01 | <0.01 | 0.02 | <0.01 | <0.01 | 0.01 | ||||||
Per 1% increase | −0.07 (−0.08, −0.06) | −0.06 (−0.07, −0.05) | −0.02 (−0.03, −0.002) | −0.07 (−0.08, −0.06) | −0.06 (−0.07, −0.05) | −0.01 (−0.02, −0.003) |
Note: V measures = V75 erosion, low resolution.
aMV-adjusted model includes age (years, continuous), race (white/nonwhite), personal history of benign breast disease (yes/no), family history of breast cancer (yes/no), parity/age at first birth (nulliparous, 1–2 births/<25 years, 1–2 births/25–29 years, 1–2 births/≥30 years, ≥3 births/<25 years, ≥3 births/≥25 years, parous/missing age at first birth), alcohol use (0, 0.1–4.9, 5.0–14.9, ≥15 g/d, missing), smoking (never, former, current), breastfeeding (<1, 1–6, 7–12, ≥13 months), and, in postmenopausal women, age at menopause (≤44, 45–49, 50–54, ≥55 years, missing) and postmenopausal hormone use (never, former, current). Models for change in BMI since age 18 years additionally include BMI at age 18 (kg/m2).
bAdditionally includes childhood body fatness (level 1–4.5+, continuous) in the MV-adjusted model.
cAdditionally includes childhood body fatness (level 1–4.5+, continuous) and percent mammographic density (square-root transformed, continuous) in the MV-adjusted model.
dPredicted body fat mass and percent fat mass at mammogram were calculated using the formula developed in the NHANES on the basis of age, race, height, weight, and waist circumference. Because 622 premenopausal and 483 postmenopausal women were missing information on waist circumference, 1,078 premenopausal and 1,464 postmenopausal women were included in these analyses.
Adult height
In both pre- and postmenopausal women, adult height (≥67.0 vs. <63.0 inches) was not associated with V (MV model: β = −0.03; 95% CI, −0.16 to 0.11, P trend = 0.67 in premenopausal; β = 0.08; 95% CI, −0.05 to 0.21, P trend = 0.61 in postmenopausal; Table 4).
. | Beta coefficients (95% CIs) . | |||
---|---|---|---|---|
. | Premenopausal women (N = 1,700) . | Postmenopausal women (N = 1,947) . | ||
. | N . | MV-adjusteda . | N . | MV-adjusteda . |
Height, inches | ||||
<63.0 | 294 | 0 (Ref) | 377 | 0 (Ref) |
63.0–64.9 | 518 | 0.001 (−0.13, 0.13) | 601 | 0.20 (0.08, 0.32) |
65.0–65.9 | 232 | −0.06 (−0.21, 0.10) | 278 | 0.10 (−0.04, 0.24) |
66.0–66.9 | 220 | 0.001 (−0.16, 0.16) | 258 | 0.13 (−0.01, 0.28) |
≥67.0 | 436 | −0.03 (−0.16, 0.11) | 433 | 0.08 (−0.05, 0.21) |
P trend | 0.67 | 0.61 | ||
Per 1-inch increase | −0.005 (−0.03, 0.02) | 0.005 (−0.01, 0.03) |
. | Beta coefficients (95% CIs) . | |||
---|---|---|---|---|
. | Premenopausal women (N = 1,700) . | Postmenopausal women (N = 1,947) . | ||
. | N . | MV-adjusteda . | N . | MV-adjusteda . |
Height, inches | ||||
<63.0 | 294 | 0 (Ref) | 377 | 0 (Ref) |
63.0–64.9 | 518 | 0.001 (−0.13, 0.13) | 601 | 0.20 (0.08, 0.32) |
65.0–65.9 | 232 | −0.06 (−0.21, 0.10) | 278 | 0.10 (−0.04, 0.24) |
66.0–66.9 | 220 | 0.001 (−0.16, 0.16) | 258 | 0.13 (−0.01, 0.28) |
≥67.0 | 436 | −0.03 (−0.16, 0.11) | 433 | 0.08 (−0.05, 0.21) |
P trend | 0.67 | 0.61 | ||
Per 1-inch increase | −0.005 (−0.03, 0.02) | 0.005 (−0.01, 0.03) |
Note: V measures = V75 erosion, low resolution.
aMV-adjusted model includes age (years, continuous), race (white/nonwhite), personal history of benign breast disease (yes/no), family history of breast cancer (yes/no), parity/age at first birth (nulliparous, 1–2 births/<25 years, 1–2 births/25–29 years, 1–2 births/≥30 years, ≥3 births/<25 years, ≥3 births/≥25 years, parous/missing age at first birth), alcohol use (0, 0.1–4.9, 5.0–14.9, ≥15 g/d, missing), smoking (never, former, current), breastfeeding (<1, 1–6, 7–12, ≥13 months), childhood body fatness (1–4.5+ level, continuous), and, in postmenopausal women, age at menopause (≤44, 45–49, 50–54, ≥55 years, missing) and postmenopausal hormone use (never, former, current).
For body fatness measures, the associations with V tend to vary by levels of PMD (low vs. high; all P interaction < 0.05; Supplementary Table S1). For all anthropometric exposures evaluated, similar results were found with high-resolution V (Supplementary Table S2) and when we considered alternate breast erosion percentages (V65) for mammographic texture measurement and stratified by digitization method of mammograms.
Associations of early-life and adult anthropometrics with mammographic density measures (PMD, dense area, and nondense area) with and without adjustment for V are presented in Supplementary Tables S3 and S4. After adjustment for V, the associations of body fatness measures with PMD and absolute nondense area persisted (Supplementary Table S3 for premenopausal; Supplementary Table S4 for postmenopausal). Height was positively associated with PMD adjusting for V in premenopausal women but not in postmenopausal women.
Discussion
To the best of our knowledge, this study is the first to examine the relationships between anthropometrics and intensity variation on a mammogram. Among both pre- and postmenopausal women, we observed a strong inverse association of early-life body fatness with adult mammographic intensity variation measure V after adjustment for current BMI and PMD. Our data suggest that the correlations of V with other mammographic features such as PMD cannot fully explain the association and provide evidence for an independent association. Current adult BMI was also inversely associated with V but the association was largely attenuated after adjustment for PMD. Adult height was not associated with V despite its positive association with premenopausal PMD. We also confirmed inverse associations of childhood and adult body fatness with PMD and positive associations with absolute nondense area, independent of V.
Our findings of inverse associations between early-life body fatness and V are consistent with those from a British cohort of premenopausal women (18) that examined the associations with the Wolfe grade (37), a qualitative classification of parenchymal patterns that considers both breast density and some texture features (23). The strong inverse associations of early-life body fatness with both PMD and V shown in the present study also mirror the similar inverse association of early-life body fatness with breast cancer risk that has been consistently reported in previous studies (4–8). Our data support the notion that early-life body fatness may influence the lifelong risk of breast cancer through reducing intensity variation of dense tissue as well as the overall breast density. In a previous report in the NHS and NHSII, we observed that the association between early-life body fatness and breast cancer risk may be partially mediated by PMD (approximately 71%–82% in premenopausal and 26%–98% in postmenopausal women; ref. 38). It is possible that the breast density–mediated pathways may explain a greater proportion of the early-life body fatness and breast cancer relationship than what was previously estimated if texture variation (e.g., grayscale intensity variation, spatial arrangement of pixels) in mammographic density was also taken into account. Early-life body fatness is likely to have lifelong effects on breast tissue architecture and composition not mediated by adult exposures, as the associations with V and PMD were independent of adult BMI and other adult risk factors. These data are consistent with the hypothesis that the early-life period is a window of susceptibility to breast cancer during which breast tissues are particularly susceptible to stimuli. As shown in our previous report (39), early-life body fatness is also associated with lower adult levels of circulating insulin-like growth factor (IGF)-I, a known breast cancer risk factor. The possible lifelong IGF-1 reduction associated with early-life body fatness may represent a potential link between early-life body fatness and adult mammographic features (e.g., PMD, V). Although largely unknown, other links (e.g., tissue-specific hormone receptors, inflammation) may also exist to alter breast development and tissue composition, leading to lifelong changes in breast density and breast cancer risk. Further investigations are needed to elucidate the underlying pathomorphological characteristics and biological mechanisms related to mammographic intensity variation measures.
In contrast to our findings with early-life body fatness, we observed the associations of current adult body fatness with V were largely attenuated after adjustment for both childhood body fatness and PMD, suggesting that the associations were largely driven by correlations with childhood body fatness and PMD. However, the associations of PMD with adult body fatness persisted after adjustment for V and childhood body fatness. Our data suggest that body fatness during adulthood modifies the overall breast density but may not independently modify the intensity variation of dense tissues within the breast. Further investigations are needed to clarify the associations of current body fatness with mammographic intensity variation.
Adult height is believed to indicate early-life exposure to growth hormones that may contribute to increased breast density at young ages (21, 22). However, in the present analysis, height was not associated with V, independent of PMD, suggesting that V may not provide additional information on biological pathways of height.
We acknowledge this study has limitations. All anthropometric measures were self-reported and thus measurement error is likely to occur. However, early-life body fatness data have shown good correlations with measured data in a validation study (31). All anthropometric data were also collected prior to the mammogram and thus any resulting measurement error is likely to be nondifferential with respect to mammographic features. For mammographic density assessment, we used semiautomated Cumulus, an operator-assisted thresholding method, and thus the measurements are prone to intra- and interreader variability. However, many studies have consistently demonstrated that Cumulus produces a measure that is robust and a strong predictor of breast cancer risk (40). Digitized mammograms came from different platforms and time periods. These differences may also induce measurement variations in the V metric. However, given that these variables are unlikely to be correlated with the assessment of exposures (self-report of early-life and adult anthropometrics), it is unlikely that these variables confound the main associations but could still result in nondifferential measurement error that bias the results toward the null. Further, V indicates image intensity variation on mammograms but not necessarily the spatial arrangement of density and thus future studies are needed to further investigate the associations with texture variations using various other measures including those that capture spatial arrangement of dense tissue. Lastly, our study population was mostly white and thus our results may not be generalizable to other populations, particularly Asian women with dense breasts.
Despite these limitations, this study has important strengths. This is the first study to examine the associations of early-life and adult anthropometrics with texture variation on a mammogram. Using automated techniques and quantitative assessment of V, we reduced measurement error and increased reliability of this measure. Using data from different imaging resolutions and different cutoff points for image processing in sensitivity analyses, we observed similar results, which further supports the robustness of our results. We also adjusted for related mammographic density measures including PMD in the regression models to evaluate the associations with V independent of these correlated features. Additionally, we had a large sample size and were able to carefully adjust for a range of potential confounders.
In summary, we observed a strong inverse association of early-life body fatness with adult mammographic texture measure V, independent of current BMI and PMD. Current body fatness was suggestively associated with lower V, independent of childhood body fatness and PMD. Adult height was not associated with V. These findings suggest that early-life body fatness may have lifelong impact on breast tissue architecture beyond breast density (dense vs. nondense tissue).
Disclosure of Potential Conflicts of Interest
No potential conflicts of interest were disclosed.
Authors' Contributions
Conception and design: M.S. Rice, E.T. Warner, J.J. Heine, R.M. Tamimi
Development of methodology: H. Oh, E.T. Warner, J.J. Heine, R.M. Tamimi
Acquisition of data (provided animals, acquired and managed patients, provided facilities, etc.): A.H. Eliassen, J.J. Heine, R.M. Tamimi
Analysis and interpretation of data (e.g., statistical analysis, biostatistics, computational analysis): H. Oh, M.S. Rice, E.T. Warner, K.A. Bertrand, E.E. Fowler, B.A. Rosner, J.J. Heine, R.M. Tamimi
Writing, review, and/or revision of the manuscript: H. Oh, M.S. Rice, E.T. Warner, K.A. Bertrand, A.H. Eliassen, B.A. Rosner, J.J. Heine, R.M. Tamimi
Administrative, technical, or material support (i.e., reporting or organizing data, constructing databases): E.E. Fowler, A.H. Eliassen, J.J. Heine, R.M. Tamimi
Study supervision: R.M. Tamimi
Acknowledgments
We would like to thank the participants and staff of the NHS and NHSII for their valuable contributions as well as the following state cancer registries for their help: AL, AZ, AR, CA, CO, CT, DE, FL, GA, ID, IL, IN, IA, KY, LA, ME, MD, MA, MI, NE, NH, NJ, NY, NC, ND, OH, OK, OR, PA, RI, SC, TN, TX, VA, WA, WY. The authors assume full responsibility for analyses and interpretation of these data. This work was supported by the NCI at the NIH (R.M. Tamimi, grant number CA131332, CA175080, P01 CA087969; A.H. Eliassen, grant number UM1 CA186107 and UM1 CA176726; J.J. Heine, grant number U01 CA200464; E.T. Warner, grant number K01CA188075), Avon Foundation for Women, Susan G. Komen for the Cure, and Breast Cancer Research Foundation. H. Oh was supported by the National Research Foundation of Korea (NRF) grant (NRF-2019R1G1A1004227, NRF-2019S1A3A2099973), Korea University Grant (K1808781), and Korea University Research Institute of Health Sciences Grant. K.A. Bertrand was supported by the Dahod Breast Cancer Research Program at Boston University School of Medicine.
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