Pregnancy and weaning regulate human maternal liver size and function
Alexandra Q. Bartlett, Kimberly K. Vesco, Jonathan Q. Purnell, Melanie Francisco, Erica T. Goddard, Xiangnan Guan, Andrea E. DeBarber, Michael C. Leo, Eric Baetscher, William D. Rooney, Willscott E. Naugler, Alexander R. Guimarães, Patrick Catalano, Zheng Xia, Pepper Schedin
Abstract
During pregnancy, the rodent liver undergoes hepatocyte proliferation and increases in size, followed by weaning-induced involution via hepatocyte cell death and stromal remodeling, creating a prometastatic niche. These data suggest a mechanism for increased liver metastasis in breast cancer patients with recent childbirth. It is unknown whether the human liver changes in size and function during pregnancy and weaning. In this study, abdominal imaging was obtained in healthy women at early and late pregnancy and postwean. During pregnancy time points, glucose production and utilization and circulating bile acids were measured. Independently of weight gain, most women's livers increased in size with pregnancy, then returned to baseline postwean. Putative roles for bile acids in liver growth and regression were observed. Together, the data support the hypothesis that the human liver is regulated by reproductive state with growth during pregnancy and volume loss postwean. These findings have implications for sex-specific liver diseases and for breast cancer outcomes.