期刊文献+

Osteoporosis and fractures in liver disease: Relevance, pathogenesis and therapeutic implications 被引量:21

Osteoporosis and fractures in liver disease: Relevance, pathogenesis and therapeutic implications
下载PDF
导出
摘要 It is being increasingly recognized that patients with liver disease develop bone loss that can be severe enough to lead to atraumatic fractures and thus markedly diminish life quality and expectancy. The estimated prevalence for liver-related osteoporosis is between 20-420/100000 of the general population, and fractures between 60-880/100000. It should be kept in mind that up to 40% of patients with chronic liver disease may experience a fracture. The pathogenic mediators include fibronectin, insulin like growth factor-I, and various cytokines, but decreased vitamin D and/or treatment with corticosteroids contribute to worsening bone health. Despite the advances in bone biology that have shed some light on the pathogenesis of this bone loss, treatment options remain nonspecific and tightly linked to treatments of other forms of osteoporosis. Thus, treatment should include calcium and vitamin D supplementation in all patients with chronic liver disease. Therapy with bisphosphonates should be considered, especially in patients receiving corticosteroids. This review focuses on the prevalence of this entity as well as the evidence available with regard to the pathogenesis of bone loss in liver disease, the diagnostic steps required in all patients, and the therapeutic options available. It is being increasingly recognized that patients with liver disease develop bone loss that can be severe enough to lead to atraumatic fractures and thus markedly diminish life quality and expectancy.The estimated prevalence for liver-related osteoporosis is between20-420/100000 of the general population,and fractures between 60-880/100000.It should be kept in mind that up to 40%of patients with chronic liver disease may experience a fracture.The pathogenic mediators include fibronectin,insulin like growth factor-Ⅰ,and various cytokines,but decreased vitamin D and/or treatment with corticosteroids contribute to worsening bone health.Despite the advances in bone biology that have shed some light on the pathogenesis of this bone loss,treatment options remain nonspecific and tightly linked to treatments of other forms of osteoporosis.Thus,treatment should include calcium and vitamin D supplementation in all patients with chronic liver disease.Therapy with bisphosphonates should be considered,especially in patients receiving corticosteroids.This review focuses on the prevalence of this entity as well as the evidence available with regard to the pathogenesis of bone loss in liver disease,the diagnostic steps required in all patients,and the therapeutic options available.
出处 《World Journal of Gastroenterology》 SCIE CAS 2014年第28期9427-9438,共12页 世界胃肠病学杂志(英文版)
关键词 OSTEOPOROSIS Liver disease Fracture Prevalence PATHOGENESIS FIBRONECTIN Insulin like growth factor-Ⅰ Therapy Vitamin D Calcium Osteoporosis Liver disease Fracture Prevalence Pat
  • 相关文献

参考文献13

  • 1Yan Ding,Lei Zhao,Hong Mei,Zhi-Hua Huang,Shu-Ling Zhang.Alterations of biliary biochemical constituents and cytokines in infantile hepatitis syndrome[J].World Journal of Gastroenterology,2006,12(43):7038-7041. 被引量:19
  • 2Schalk W van der Merwe,Maria M Conradie,Robert Bond,Brenda J Olivier,Elongo Fritz,Martin Nieuwoudt,Rhena Delport,Tomas Slavik,Gert Engelbrecht,Del Kahn,Enid G Shephard,Maritha J Kotze,Nico P de Villiers,Stephen Hough.Effect of rapamycin on hepatic osteodystrophy in rats with portasystemic shunting[J].World Journal of Gastroenterology,2006,12(28):4504-4510. 被引量:2
  • 3Ingolf Schiefke,Andreas Fach,Marcus Wiedmann,Andreas V.Aretin,Eva Schenker,Gudrun Borte,Manfred Wiese,Joachim Moessner.Reduced bone mineral density and altered bone turnover markers in patients with non-cirrhotic chronic hepatitis B or C infection[J].World Journal of Gastroenterology,2005,11(12):1843-1847. 被引量:24
  • 4J. L. Casado,S. Ba?on,R. Andrés,M. J. Perez-Elías,A. Moreno,S. Moreno.Prevalence of causes of secondary osteoporosis and contribution to lower bone mineral density in HIV-infected patients[J].Osteoporosis International.2014(3) 被引量:1
  • 5Martin Blachier,Henri Leleu,Markus Peck-Radosavljevic,Dominique-Charles Valla,Fran?oise Roudot-Thoraval.The burden of liver disease in Europe: A review of available epidemiological data[J].Journal of Hepatology.2013(3) 被引量:16
  • 6Masanobu Kawai,Clifford J. Rosen.The Insulin-Like Growth Factor System in Bone[J].Endocrinology and Metabolism Clinics of North America.2012(2) 被引量:1
  • 7Seong-Su Moon,Young-Sil Lee,Sung Kim.Association of nonalcoholic fatty liver disease with low bone mass in postmenopausal women[J].Endocrine.2012(2) 被引量:1
  • 8Ghizlane Wariaghli,Fadoua Allali,Abdellah El Maghraoui,Najia Hajjaj-Hassouni.Osteoporosis in patients with primary biliary cirrhosis[J].European Journal of Gastroenterology & Hepatology.2010(12) 被引量:1
  • 9.Low Bone Mass and Severity of Cholestasis Affect Fracture Risk in Patients With Primary Biliary Cirrhosis[J].Gastroenterology.2010(7) 被引量:1
  • 10AnkeBentmann,NinaKawelke,DavidMoss,HanswalterZentgraf,YohannBala,IrinaBerger,Juerg AGasser,Inaam ANakchbandi.Circulating fibronectin affects bone matrix, whereas osteoblast fibronectin modulates osteoblast function[J].J Bone Miner Res.2010(4) 被引量:1

二级参考文献74

  • 1[1]Iber F.Bone disease in chronic liver disease.Am J Gastroenterol 1989; 84:1229-1230 被引量:1
  • 2[2]Rouillard S,Lane NE.Hepatic osteodystrophy.Hepatology 2001; 33:301-307 被引量:1
  • 3[3]Stellon AJ,Webb A,Compston JE.Bone histomorphometry and structure in corticosteroid treated chronic active hepatitis.Gut 1988; 29:378-384 被引量:1
  • 4[4]Hodgson SF,Dickson ER,Wahner HW,Johnson KA,Mann KG,Riggs BL.Bone loss and reduced osteoblast function in primary biliary cirrhosis.Ann Intern Med 1985; 103:855-860 被引量:1
  • 5[5]Guanabens N,Pares A,Marinoso L,Brancos MA,Piera C,Serrano S,Rivera F,Rodes J.Factors influencing the development of metabolic bone disease in primary biliary cirrhosis.Am J Gastroenterol 1990; 85:1356-1362 被引量:1
  • 6[6]Bonkovsky HL,Hawkins M,Steinberg K,Hersh T,Galambos JT,Henderson JM,Millikan WJ,Galloway JR.Prevalence and prediction of osteopenia in chronic liver disease.Hepatology 1990; 12:273-280 被引量:1
  • 7[7]Gonzalez-Calvin JL,Garcia-Sanchez A,Bellot V,MunozTorres M,Raya-Alvarez E,Salvatierra-Rios D.Mineral metabolism,osteoblastic function and bone mass in chronic alcoholism.Alcohol Alcohol 1993; 28:571-579 被引量:1
  • 8[8]Gallego-Rojo FJ,Gonzalez-Calvin JL,Munoz-Torres M,Mundi JL,Fernandez-Perez R,Rodrigo-Moreno D.Bone mineral density,serum insulin-like growth factor I,and bone turnover markers in viral cirrhosis.Hepatology 1998; 28:695-699 被引量:1
  • 9[9]Ross PD,Davis JW,Epstein RS,Wasnich RD.Pre-existing fractures and bone mass predict vertebral fracture incidence in women.Ann Intern Med 1991; 114:919-923 被引量:1
  • 10[10]Cummings SR,Black DM,Nevitt MC,Browner W,Cauley J,Ensrud K,Genant HK,Palermo L,Scott J,Vogt TM.Bone density at various sites for prediction of hip fractures.The Study of Osteoporotic Fractures Research Group.Lancet 1993;341:72-75 被引量:1

共引文献57

同被引文献150

引证文献21

二级引证文献88

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部