Faculty of Medicine and Health Sciences, Department of Public Health and Nursing, Norwegian University of Science and Technology, Post box 8905, N-7491, Trondheim, Norway.
The Cancer Clinic, St. Olavs Hospital, Trondheim University Hospital, Trondheim, Norway.
BMC Cancer. 2021 Mar 23;21(1):299. doi: 10.1186/s12885-021-08027-9.
Because birth size appears to be positively associated with breast cancer risk, we have studied whether this risk may differ according to molecular breast cancer subtypes.
A cohort of 22,931 women born 1920-1966 were followed up for breast cancer occurrence from 1961 to 2012, and 870 were diagnosed during follow-up. Archival diagnostic material from 537 patients was available to determine molecular breast cancer subtype, specified as Luminal A, Luminal B (human epidermal growth factor receptor 2 (HER2)-), Luminal B (HER2+), HER2 type, and Triple negative (TN) breast cancer. Information on the women's birth weight, birth length and head circumference at birth was used to estimate hazard ratios (HR) with 95% confidence intervals (CI) for each molecular subtype, applying Cox regression, and stratified by maternal height.
Birth length (per 2 cm increments) was positively associated with Luminal A (HR = 1.2, 95% CI, 1.0-1.3), Luminal B (HER2+) (HR = 1.3, 95% CI, 1.0-1.7), and TN breast cancer (HR = 1.4, 95% CI, 1.0-1.9). No clear association was found for birth weight and head circumference. The positive associations of birth length were restricted to women whose mothers were relatively tall (above population median).
We found a positive association of birth length with risk of Luminal A, Luminal B (HER2+) and TN breast cancer that appears to be restricted to women whose mothers were relatively tall. This may support the hypothesis that breast cancer risk is influenced by determinants of longitudinal growth and that this finding deserves further scrutiny.
由于出生体重似乎与乳腺癌风险呈正相关,我们研究了这种风险是否可能因分子乳腺癌亚型而异。
我们对 1920 年至 1966 年出生的 22931 名女性进行了队列研究,从 1961 年到 2012 年随访乳腺癌的发生情况,在随访期间有 870 名被诊断患有乳腺癌。有 537 名患者的存档诊断材料可用于确定分子乳腺癌亚型,具体为 Luminal A、Luminal B(人表皮生长因子受体 2(HER2-))、Luminal B(HER2+)、HER2 型和三阴性(TN)乳腺癌。利用 Cox 回归,根据母亲身高分层,应用出生体重、出生长度和出生时头围来估计每个分子亚型的危险比(HR)及其 95%置信区间(CI)。
出生长度(每增加 2 厘米)与 Luminal A(HR=1.2,95%CI,1.0-1.3)、Luminal B(HER2+)(HR=1.3,95%CI,1.0-1.7)和 TN 乳腺癌(HR=1.4,95%CI,1.0-1.9)呈正相关。出生体重和头围与风险无明显相关性。出生长度的正相关仅见于母亲相对较高(高于人群中位数)的女性。
我们发现出生长度与 Luminal A、Luminal B(HER2+)和 TN 乳腺癌风险呈正相关,这种相关性似乎仅限于母亲相对较高的女性。这可能支持乳腺癌风险受纵向生长决定因素影响的假说,这一发现值得进一步研究。