USCAP 2022 Abstracts: Liver Pathology (1018-1075)

Rhonda Yantiss Chair, Kristin Jensen Chair, Cme Subcommittee, Laura C. Collins, Yuri Fedoriw, Ilan Weinreb, Carla Chair,Adebowale Adeniran, Kimberly H. Allison, Sarah Dry, William C. Faquin,Karen Fritchie, Jennifer Gordetsky, Levon Katsakhyan, Pathologist-In-Training Melinda, J Lerwill, M Beatriz, Susana Lopes, Julia Naso, Pathologist-In-Training Liron, Pantanowitz Carlos, Parra-Herran Rajiv, Mayank Patel, Matt Quick, David F. Schaeffer, Lynette M. Sholl, Olga K. Weinberg, Maria Westerhoff, Benjamin Adam, Oyedele Adeyi, Mariam P. Alexander,Daniela Allende,Catalina Amador, Vijayalakshmi Ananthanarayanan,Tatjana Antic,Manju Aron,Roberto Barrios, Gregory Bean Govind, Bhagat Luis, Zabala Blanco, Michael Bonert,Alain Borczuk, Tamar Brandler, Eric Burks, Kelly J. Butnor, Sarah Calkins, Weibiao Cao, Cristina Bárbara, Alberto Centeno, Joanne Sy, Chan Kung-Chao,Chang Hao, Chen, Yunn-Yi Chen, Sarah Chiang, Soo‐Jin Cho,Shefali Chopra, Nicole A. Cipriani, Cecilia Clement, Claudiu Cotta, Jennifer Cotter, Sonika Dahiya, Elizabeth G. Demicco, Katie Dennis, Jasreman Dhillon, Anand S. Dighe, Bojana Djordjevic, Michelle Downes, Charles G. Eberhart, Andrew Evans, Fang Fan,Julie C. Fanburg‐Smith, Gelareh Farshid,Michael Feely, Susan Fineberg, Dennis Firchau, Gregory A. Fishbein, Agnes B. Fogo,Andrew L. Folpe, Danielle Fortuna, Billie Fyfe-Kirschner, Zeina Ghorab, Giovanna A. Giannico, Anthony J. Gill, Tamar Giorgadze, Alessio Giubellino, Carolyn Glass, Carmen Gomez‐Fernandez, Shunyou Gong, Purva Gopal, Abha Goyal, Christopher Griffith, Ian S. Hagemann, Gillian Leigh, Hale Suntrea, T Hammer,Malini Harigopal, Kammi Henriksen, Jonas J. Heymann, Carlo Hojilla, Aaron Huber, Jabed Iqbal, Shilpa Jain, Vickie Y. Jo, Ivy John, Dan Jones, Ridas Juskevicius, Meghan Kapp, Nora Katabi, Francesca Khani, Joseph D. Khoury, Benjamin R. Kipp,Veronica Klepeis, Christian A. Kunder, Stefano La, Rosa Stephen, M Laganà, Keith Lai, Goo Lee, Michael Lee, Vasiliki Leventaki, Madelyn Lew, Faqian Li, Ying Liu, Chieh‐Yu Lin, Mikhail Lisovsky, Lesley Lomo, Fang‐I Lu, Ma Varsha, Manucha Rachel, Angelica Mariani, Brock Aaron, David Martin, Shannon D. McClintock, Anne M. Mills, Eesha Acharya,Robert Lam,Joseph K. Lim,Dhanpat Jain, Sameer Al Diffalha, Chirag Patel, Prachi Bajpai, Amr Elkholy, Michael Behring, Brandon Wilk, Manavalan Gajapathy,Felipe Massicano, Tarun Karthik, Kumar Mamidi, Donna Brown, Gurpreet Kaur, Abby Shelton, Erin Smithberger, George J. Netto,Ryan Miller, Elizabeth A. Worthey, Upender Manne, Leticia Bornstein-Quevedo, Claudia Bautista-Wong, Zaira Mojica-Gonzalez, E. Martínez Molina, Gabriel Herrera‐Maya, Novo Nordisk, Claudia J. Bautista, Joeffrey Chahine, Sumeyye Culfaci,Dong Hyang Kwon, Pamela L. Tuma,Bhaskar Kallakury,Andreas Ciscato, Alex Placek, Homayoun Mostaghni,Mojgan Hosseini–Varnamkhasti

Modern pathology(2022)

引用 0|浏览1
暂无评分
摘要
Background: Men and post-menopausal women are at increased risk of developing non-alcoholic steatohepatitis (NASH) compared to pre-menopausal women.However, the impact of age and gender on NASH progression remains controversial.We sought to investigate whether age and gender were associated with severity of nonalcoholic steatohepatitis (NASH).Design: From a cohort of adult patients with biopsy-proven NASH from 2012-2019, we conducted a cross-sectional study with patients stratified by age and gender (men 18-50 years, women 18-50 years, men >50 years, women >50 years).Twenty-five patients were randomly selected into each group.Patients with a prior liver transplant or alternative etiologies were excluded, including autoimmune and viral hepatitis, alcoholic liver disease, and genetic and other metabolic disorders.Baseline anthropometric data at the time of the index liver biopsy date were obtained.Each patient's liver biopsy was evaluated for a variety of histologic factors, including steatosis, fibrosis (NASH-CRN criteria) and nonalcoholic fatty liver disease activity score (NAS).ANOVA tests were performed to calculate differences between age and gender groups for various clinical and histologic parameters.Results: A summary of descriptive results for the various age and gender groups is show in Table 1.Baseline mean age was similar among corresponding age groups, and BMI was similar across all groups.Among histologic features, there was a significant difference among age and gender groups for NAS (p=0.02) and fibrosis (p<0.001).The degree of steatosis (mean 2.3, SD 0.8) and NAS (mean 4.5, SD 0.9) were highest in 18-50 year-old women compared to >50 year-old women and men of all ages.Fibrosis scores were higher in men compared to women for all age groups, and was highest in >50 year-old men (mean 2.8, SD 1.2).Men, 18-50 years Mean (SD) Female, 18-50 years Mean (SD) Male, >50 years Mean (SD)Conclusions: An association between age and gender with severity of NASH was observed.Women have higher steatosis and NAS compared to men.However, liver fibrosis tends to be more severe in men, and tends to increase with age irrespective of gender.Estrogen-related sex hormones may play a protective role against fibrosis in young pre-menopausal women.This phenomenon may have therapeutic implications and needs further evaluation.
更多
查看译文
AI 理解论文
溯源树
样例
生成溯源树,研究论文发展脉络
Chat Paper
正在生成论文摘要