导师风采
李梅

个人信息

Personal Information

  • 性别:女
  • 导师类型:博导
  • 职称:主任医师
  • 该职称任职时间:20010823

联系方式

Contact Information

  • 所属院系:北京协和医院
  • 所属专业:
  • 邮箱 : limeilzh@sina.com
  • 工作电话 : 010-69155088

个人简介

Personal Profile

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。

  • 研究方向Research Directions
骨质疏松症等代谢性及遗传性骨病
  • 在校研究生Current Graduate Students

硕士研究生 1 名,博士研究生 4 名

  • 科研项目Research Projects
# 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 —— 2021-12-03200万元主持的企业/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 —— 2022-12-01100万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
9PLS3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
  • 发表论文Papers
# 论文题目 期刊名称 发表年份 论文署名
1Novel mutations in BMP1 induce a rare type of osteogenesis imperfectaCLIN CHIM ACTA2019-02-01通讯作者
2Health-related quality of life in children with osteogenesis imperfecta: a large-sample studyOSTEOPOROSIS INT2019-02-01通讯作者
3Genotype-phenotype relationship in a large cohort of osteogenesis imperfecta patients with COL1A1 mutations revealed by a new scoring systemCHINESE MED J-PEKING2019-01-01通讯作者
4A novel heterozygous missense mutation in P4HB causes mild type osteogenesis imperfecta and response to bisphosphonates.Biosci Rep.2019-04-30通讯作者
5Effects of zoledronic acid on vertebral shape of children and adolescents with osteogenesis imperfectaBONE2019-10-01通讯作者
6Effects of bisphosponates on osteoporosis induced by Duchenne muscular dystrophy: a prospective studyEndocrine practice2020-12-01通讯作者
7Novel Variants In Col2a1 Causing Rare Spondyloepiphyseal Dysplasia CongenitaMolecular Genetics & Genomic Medicine2020-03-03通讯作者
8A Novel Variant In Aire Causing A Rare,Non‑Classical Autoimmune Polyendocrine Syndrome Type 1Molecular Medicine Reports2020-06-12通讯作者
9A novel mutation in PLS3 causes extremely rare X-linked osteogenesis imperfectaMolecular genetics & genomic medicine2020-11-01通讯作者
10Clinical, Biochemical, Radiological, and Genetic Analyses of a Patient with VCP Gene Variant-Induced Paget's Disease of BoneCalcif Tissue Int2021-11-20通讯作者
11Specific Characteristic of Hyperplastic Callus in a Larger Cohort of Osteogenesis Imperfecta Type VCALCIFIED TISSUE INTERNATIONAL2022-04-01通讯作者
12Effects of Bisphosphonates on Bone of Osteoporotic Men With Different Androgen Levels: A Case-Control StudyEndocrine Practice2022-03-01通讯作者
13The Risk Factors for Developing Clustered Vertebral Compression Fractures: A Single-Center StudyEndocrine Practice2022-03-01通讯作者
14Relationship of Pathogenic Mutations and Responses to Zoledronic Acid in a Cohort of Osteogenesis Imperfecta ChildrenJOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM2022-08-18通讯作者
15The role of osteocalcin in regulation of glycolipid metabolism and muscle function in children with osteogenesis imperfectaFrontiers in Endocrinology2022-08-02通讯作者
16Skeletal outcomes of patients with osteogenesis imperfecta during drug holiday of bisphosphonates: a real-world studyFrontiers in Endocrinology2022-09-26通讯作者
17Cardiovascular abnormalities and its correlation with genotypes of children with osteogenesis imperfectaFrontiers in Endocrinology2022-10-20通讯作者
18Novel mutation in LRP5 gene cause rare osteosclerosis: cases studies and literature reviewMOLECULAR GENETICS AND GENOMICS2023-03-27通讯作者
19The roles of sclerostin and irisin on bone and muscle of orchiectomized ratsBMC MUSCULOSKELETAL DISORDERS2022-12-02通讯作者
20Genotypic and phenotypic spectrum and pathogenesis of WNT1 variants in a large cohort of patients with OI/osteoporosisJOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM2023-01-03通讯作者
21Health-related quality of life of men with primary osteoporosis and its changes after bisphosphonates treatmentBMC MUSCULOSKELETAL DISORDERS2023-04-19通讯作者
22Impaired bone strength and bone microstructure in a novel early-onset osteoporotic rat model with a clinically relevant PLS3 mutationeLife2023-04-21通讯作者
23Genotype-phenotype relationship and comparison between eastern and western patients with osteogenesis imperfectaJOURNAL OF ENDOCRINOLOGICAL INVESTIGATION2023-06-04通讯作者
24Ultra-High Performance Liquid Chromatography-Mass Spectrometry-based Serum Metabolomics for Early Diagnosis of Refractory Tumor-induced Osteomalacia: A Case-control StudyJOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM2023-01-31通讯作者
25Correlation of lipocalin 2 and glycolipid metabolism and body composition in a large cohort of children with osteogenesis imperfectaJOURNAL OF ENDOCRINOLOGICAL INVESTIGATION2023-06-16通讯作者
26Pathogenesis and treatment of osteoporosis in patients with hemophiliaArchives of Osteoporosis2023-01-14通讯作者
27Health-related quality of life in men with osteoporosis: a systematic review and meta-analysisENDOCRINE2021-06-24通讯作者
28Genetic Analysis, Phenotypic Spectrum and Functional Study of Rare Osteogenesis Imperfecta Caused by CRTAP VariantsJOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM2024-01-12通讯作者
29Efficacy and safety of denosumab versus zoledronic acid in OI adults: A prospective, open-label, randomized studyJOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM2024-01-05通讯作者
30Correlation of serum DKK1 level with skeletal phenotype in children with osteogenesis imperfectaJOURNAL OF ENDOCRINOLOGICAL INVESTIGATION2024-05-14通讯作者
31Safety and Efficacy of Denosumab in Children With Osteogenesis Imperfecta—the First Prospective Comparative StudyJOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM2024-01-10通讯作者
32Alzheimer's disease and its associated risk of bone fractures: a narrative reviewFrontiers in Endocrinology2023-08-09通讯作者
33Efficacy of Yigu versus Aclasta in Chinese postmenopausal women with osteoporosis: a multicenter prospective studyArchives of Osteoporosis2022-01-12第一作者
34Efficacy of generic teriparatide and alendronate in Chinese postmenopausal women with osteoporosis: a prospective studyArchives of Osteoporosis2022-07-28第一作者
  • 科研获奖Research Awards
# 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
120193202472P4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14
22019-219-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14
  • 研究成果Research Findings
# 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