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个人简介
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李梅,医学博士,主任医师,博士研究生及博士后导师,现任北京协和医院内分泌科副主任。兼任中华医学会骨质疏松和骨矿盐疾病学分会候任主委,北京医学会骨质疏松和骨矿盐疾病分会候任主任委员,中国研究型医院学会罕见病分会理事,国家健康科普专家库专家。担任《中华骨质疏松和骨矿盐疾病杂志》副主编及编辑部主任,任《The Journal of Clinical Endocrinology & Metabolism》、《中国全科医学杂志》、《基础医学与临床杂志》编委。擅长多种内分泌代谢性疾病,尤其是骨质疏松症等代谢性、遗传性骨骼疾病的临床诊治、基础研究及健康科普宣教。主持国家自然科学基金项目6项,以第一或通讯作者,在eLIFE、The Journal of Clinical Endocrinology & Metabolism、Bone、Osteoporosis International、Endocrine等杂志发表论著200余篇,牵头或参与制定国内外骨骼疾病相关指南20部。研究成果获得华夏医学科技进步一等奖、教育部高校科技进步二等奖。
团队简介
Team Profile
研究团队主要从事多种内分泌疾病,尤其是骨质疏松症等代谢性及遗传性骨病的基础研究及临床诊治工作。聚焦遗传性及代谢性骨骼疾病,建立动物模型,深入探讨疾病分子机制及积极聚焦新药研发,在eLIFE、The Journal of Clinical Endocrinology & Metabolism、Bone、Osteoporosis International、Endocrine等杂志发表论著200余篇。
硕士研究生 1 名,博士研究生 4 名
# | 项目名称 | 起止日期 | 金额 | 项目类型 | 本人角色 |
---|---|---|---|---|---|
1 | 先天性骨骼畸形的致病机制及干预研究 | 2016-12-03 —— 2021-12-03 | 200万元 | 主持的企业/行业委托重大项目 | 主持人 |
2 | 通过调控骨转换失衡建立男性骨质疏松症新型精准治疗策略研究 | 2021-09-01 —— 2023-08-31 | 主持的企业/行业委托重大项目 | 主持人 | |
3 | 基于国人骨折风险的新型骨质疏松精准诊疗体系建立 | 2022-10-01 —— 2025-09-01 | 主持的企业/行业委托重大项目 | 主持人 | |
4 | 基于I型胶原调控网络的骨质疏松症早期预警及机制研究 | 2020-01-01 —— 2022-12-01 | 主持在研的国家或省部级科研项目 | 主持人 | |
5 | 遗传性钙磷代谢障碍对儿童骨骼等器官发育的影响及机制研究 | 2019-01-01 —— 2022-12-01 | 100万元 | 主持在研的国家或省部级科研项目 | 主持人 |
6 | 骨质疏松症新型靶向治疗药物研究 | 2021-12-01 —— 2024-11-01 | 主持在研的国家或省部级科研项目 | 主持人 | |
7 | 成骨不全症新型二代捕获测序平台的建立及准确校正致病基因突变的分子靶向治疗探索 | 2016-01-01 —— 2019-12-06 | 主持在研的国家或省部级科研项目 | 主持人 | |
8 | 从SERPINH1-Wnt/β-连环素通路探索骨质疏松性骨折高风险的遗传调控新机制及核酸适配子靶向治疗新策略 | 2024-01-01 —— 2027-12-31 | 主持在研的国家或省部级科研项目 | 主持人 | |
9 | PLS3基因通过骨基质蛋白代谢通路调控骨质疏松症的新机制及治疗新靶点的研究 | 2021-01-01 —— 2024-12-31 | 主持在研的国家或省部级科研项目 | 主持人 | |
10 | 从重要的骨基质蛋白代谢通路探索原发性骨质疏松症早期诊治的新靶点 | 2019-01-01 —— 2022-12-01 | 主持在研的国家或省部级科研项目 | 主持人 |
# | 论文题目 | 期刊名称 | 发表年份 | 论文署名 |
---|---|---|---|---|
1 | Novel mutations in BMP1 induce a rare type of osteogenesis imperfecta | CLIN CHIM ACTA | 2019-02-01 | 通讯作者 |
2 | Health-related quality of life in children with osteogenesis imperfecta: a large-sample study | OSTEOPOROSIS INT | 2019-02-01 | 通讯作者 |
3 | Genotype-phenotype relationship in a large cohort of osteogenesis imperfecta patients with COL1A1 mutations revealed by a new scoring system | CHINESE MED J-PEKING | 2019-01-01 | 通讯作者 |
4 | A novel heterozygous missense mutation in P4HB causes mild type osteogenesis imperfecta and response to bisphosphonates. | Biosci Rep. | 2019-04-30 | 通讯作者 |
5 | Effects of zoledronic acid on vertebral shape of children and adolescents with osteogenesis imperfecta | BONE | 2019-10-01 | 通讯作者 |
6 | Effects of bisphosponates on osteoporosis induced by Duchenne muscular dystrophy: a prospective study | Endocrine practice | 2020-12-01 | 通讯作者 |
7 | Novel Variants In Col2a1 Causing Rare Spondyloepiphyseal Dysplasia Congenita | Molecular Genetics & Genomic Medicine | 2020-03-03 | 通讯作者 |
8 | A Novel Variant In Aire Causing A Rare,Non‑Classical Autoimmune Polyendocrine Syndrome Type 1 | Molecular Medicine Reports | 2020-06-12 | 通讯作者 |
9 | A novel mutation in PLS3 causes extremely rare X-linked osteogenesis imperfecta | Molecular genetics & genomic medicine | 2020-11-01 | 通讯作者 |
10 | Clinical, Biochemical, Radiological, and Genetic Analyses of a Patient with VCP Gene Variant-Induced Paget's Disease of Bone | Calcif Tissue Int | 2021-11-20 | 通讯作者 |
11 | Specific Characteristic of Hyperplastic Callus in a Larger Cohort of Osteogenesis Imperfecta Type V | CALCIFIED TISSUE INTERNATIONAL | 2022-04-01 | 通讯作者 |
12 | Effects of Bisphosphonates on Bone of Osteoporotic Men With Different Androgen Levels: A Case-Control Study | Endocrine Practice | 2022-03-01 | 通讯作者 |
13 | The Risk Factors for Developing Clustered Vertebral Compression Fractures: A Single-Center Study | Endocrine Practice | 2022-03-01 | 通讯作者 |
14 | Relationship of Pathogenic Mutations and Responses to Zoledronic Acid in a Cohort of Osteogenesis Imperfecta Children | JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM | 2022-08-18 | 通讯作者 |
15 | The role of osteocalcin in regulation of glycolipid metabolism and muscle function in children with osteogenesis imperfecta | Frontiers in Endocrinology | 2022-08-02 | 通讯作者 |
16 | Skeletal outcomes of patients with osteogenesis imperfecta during drug holiday of bisphosphonates: a real-world study | Frontiers in Endocrinology | 2022-09-26 | 通讯作者 |
17 | Cardiovascular abnormalities and its correlation with genotypes of children with osteogenesis imperfecta | Frontiers in Endocrinology | 2022-10-20 | 通讯作者 |
18 | Novel mutation in LRP5 gene cause rare osteosclerosis: cases studies and literature review | MOLECULAR GENETICS AND GENOMICS | 2023-03-27 | 通讯作者 |
19 | The roles of sclerostin and irisin on bone and muscle of orchiectomized rats | BMC MUSCULOSKELETAL DISORDERS | 2022-12-02 | 通讯作者 |
20 | Genotypic and phenotypic spectrum and pathogenesis of WNT1 variants in a large cohort of patients with OI/osteoporosis | JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM | 2023-01-03 | 通讯作者 |
21 | Health-related quality of life of men with primary osteoporosis and its changes after bisphosphonates treatment | BMC MUSCULOSKELETAL DISORDERS | 2023-04-19 | 通讯作者 |
22 | Impaired bone strength and bone microstructure in a novel early-onset osteoporotic rat model with a clinically relevant PLS3 mutation | eLife | 2023-04-21 | 通讯作者 |
23 | Genotype-phenotype relationship and comparison between eastern and western patients with osteogenesis imperfecta | JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION | 2023-06-04 | 通讯作者 |
24 | Ultra-High Performance Liquid Chromatography-Mass Spectrometry-based Serum Metabolomics for Early Diagnosis of Refractory Tumor-induced Osteomalacia: A Case-control Study | JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM | 2023-01-31 | 通讯作者 |
25 | Correlation of lipocalin 2 and glycolipid metabolism and body composition in a large cohort of children with osteogenesis imperfecta | JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION | 2023-06-16 | 通讯作者 |
26 | Pathogenesis and treatment of osteoporosis in patients with hemophilia | Archives of Osteoporosis | 2023-01-14 | 通讯作者 |
27 | Health-related quality of life in men with osteoporosis: a systematic review and meta-analysis | ENDOCRINE | 2021-06-24 | 通讯作者 |
28 | Genetic Analysis, Phenotypic Spectrum and Functional Study of Rare Osteogenesis Imperfecta Caused by CRTAP Variants | JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM | 2024-01-12 | 通讯作者 |
29 | Efficacy and safety of denosumab versus zoledronic acid in OI adults: A prospective, open-label, randomized study | JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM | 2024-01-05 | 通讯作者 |
30 | Correlation of serum DKK1 level with skeletal phenotype in children with osteogenesis imperfecta | JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION | 2024-05-14 | 通讯作者 |
31 | Safety and Efficacy of Denosumab in Children With Osteogenesis Imperfecta—the First Prospective Comparative Study | JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM | 2024-01-10 | 通讯作者 |
32 | Alzheimer's disease and its associated risk of bone fractures: a narrative review | Frontiers in Endocrinology | 2023-08-09 | 通讯作者 |
33 | Efficacy of Yigu versus Aclasta in Chinese postmenopausal women with osteoporosis: a multicenter prospective study | Archives of Osteoporosis | 2022-01-12 | 第一作者 |
34 | Efficacy of generic teriparatide and alendronate in Chinese postmenopausal women with osteoporosis: a prospective study | Archives of Osteoporosis | 2022-07-28 | 第一作者 |
# | 获奖证书编号 | 奖项名称 | 获奖级别 | 获奖类别 | 获奖等级 | 获奖日期 | 颁奖单位 | 本单位是否为第一完成单位 | 完成单位排名 | 本人排序 | 备注 |
---|---|---|---|---|---|---|---|---|---|---|---|
1 | 20193202472P4 | 遗传性内分泌代谢疾病新型诊疗体系的建立及应用 | 国家级 | 华夏医学科技奖 | 一等奖 | 2019-12-07 | 中国医疗保健国际交流促进会 | 是 | 1 | 4 | |
2 | 2019-219-R04 | 遗传性内分泌代谢疾病新型诊疗体系的建立及应用 | 国家级 | 高等学校科学研究优秀成果奖(科学技术进步奖) | 二等奖 | 2019-12-10 | 中华人民共和国教育部 | 是 | 1 | 4 |
# | 成果类型 | 项目/专利/新品种名称 |
---|---|---|
1 | 出版高水平专著 | 维生素D与临床 |
2 | 出版高水平专著 | 协和代谢性骨病学 |
3 | 出版高水平专著 | 泌语协行 内分泌的秘密 |
4 | 出版高水平专著 | 协和内分泌疾病诊疗常规 |
5 | 出版高水平专著 | 协和内分泌科大查房 |
6 | 出版高水平专著 | 社区与基层医生骨质疏松防治培训教程 |
7 | 出版高水平专著 | 遗传性内分泌代谢疾病 |
8 | 出版高水平专著 | 《中国老年糖尿病诊疗指南(2021版)》专家解读 |
9 | 获得省部级及以上科研奖励 | 遗传性内分泌代谢疾病新型诊疗体系的建立及应用 |
10 | 获得省部级及以上科研奖励 | 遗传内分泌代谢疾病新型诊疗体系的建立及应用 |
11 | 作为主创人员获得授权的发明专利和新品种 | 新型PLS3基因敲除大鼠动物模型的构建方法和应用 |