胆盐代谢及转运和肝内胆汁淤积分子医学和临床的相互促

1、胆盐代谢及转运和肝内胆汁淤积胆盐代谢及转运和肝内胆汁淤积 分子医学和临床的相互促进分子医学和临床的相互促进 王建设复旦大学附属儿科医院复旦大学儿童肝病中心“特发性特发性”新生儿肝炎新生儿肝炎 ggt and the outcomejuly 1, 1981-jan 1, 1985, 186 infants, 29 diagnosed as inhs, followed up for at least 1 year, or until death: 17 with increased ggt (=2.1*normal upper limit), all but 1 in good prognosi

2、s 12 with normal ggt, all poor prognosismaggiore g, et al. j pediatr, 1987;112:251-252.kings病例入选标准病例入选标准 aug 1991 to nov 2000, conjugated hyperbilirubinemia under 3 months of age (973 cases) no specific etiologic factor can be ascertained after comprehensive work-up followed up for at least one year

3、 or until diedwang js, eur j pediatr, 2006, in press病例排除标准病例排除标准 inr1.2 and not be fully corrected after vitamin k injection follow up interval longer than 3 months other severe congenital abnormalities g6pd deficiency evidence of active cmv infection in spite of no inclusion found on liver biopsy u

4、ss demonstrated bile duct dilation.basic information 128 cases elected, 110 biopsyed 6 patients diagnosed as pfic 1 or 2, 1 recurred jaundice. ggt level with endpoints without endpointspresentation 29-84 52.9%100peak 36-93 13.2%50u/l组32例，3例预后不良(p=0.001) 峰值gt 100u/l进行分组 100u/l组10例，6例预后不良 100u/l组28例，2

5、例预后不良(p=0.002) 血清ggt水平和预后的有关（和cmv状态无关）王中林. 肝脏 2005，(4)进行性家族性肝内郁胆（进行性家族性肝内郁胆（pficpfic） first reported in amish family (byler disease), autosomal recessive inheritance clinical presentation: cholestasis and low ggt pruritus, epistaxis normal or near normal cholesterol, no xanthomasfic1 deficiency bric

6、 基因定位18q21-22 houwen rh, 1994, nat genet 8:380 pfic (byler disease)基因定位18q21-22 carlton ve, 1995, 4:1049-1053 pfic遗传异质性，pfic1 atp8b1基因，编码的产物fic1 bull ln, nat genet 1998, 18:219fic1 deficiency (续续) greenland familial cholestasis, asp554asn klomp lw, hepatology, 2000,32:1337 各地的散发性病例 无家族史、父母非近亲婚配 欧洲、日

7、本、中国台湾 新认识 pfic1和bric 1有同一基因引起 pfic多见缺失、移位、无义突变 bric多见错义突变 pfic1和bric 1可表现为一连续过程 共同的临床特征low ggt in cholestasislow ggt expressiondefect of bile salt exportationbsep deficiency 1997年，低ggt pfic的第二个基因（沙特）被定位于2q24，因此这种被命名为pfic2 strautnieks ss. am j hum genet. 61,630. 1998年， bsep基因突变引起pfic 2 strautnieks s

8、s. nat genet. 20,233. 2004 年，bric 2由abcb11突变 pfic多见缺失、移位、无义突变, bric多见错义突变 van mil swc, gastroenterology, 127,379. pfic 2 见于欧洲、日本、 中国等世界各地case 2 20061388 ga, a167i case 3 cag tagexon 18 c2230t q702stop case 5 intron 22 (+3) exon 7 t a 562 gt g188wcase 5 intron 22 (+3) 紧邻剪切位点(acct) t to a hum aagattac

9、ctg mus aagattacctg dog aagattacctg cow tagattacctg case aagataacctgcase 7 intron 6 t+63t/g (167) low ggt in cholestasisdefect of bile salt exportationdefect of bile salt synthesisbile acid synthetic defect 16 enzymes catalyze 17 reactions in bile acid synthesis from cholesterolrussell dw. annu rev

10、biochem 2003,72,137 defects in different enzymes associate with neonatal cholestasis delta(4)-3-oxosteroid 5beta-reductase(akr1d1)gonzales e, j hepatol 2004,40,716 oxysterol 7-hydroxylase (crp7b1)setchell kdr, j clin invest 1998,102,1690bile acid synthetic defect -pfic 4 2000, hsd3b7, chromosome 16p

11、12-p11.2 encoding 3-beta-hydroxy-delta-5-c27 steroid oxidoreductase (c27-3-beta-hsd) participate in all pathways of bile acid synthesis (7-alpha-hydroxylated sterols) 2 bp deletion in a saudi boy with neonatal picschwarz m. j clin invest 2000,106,1175 2003, confirmed in a chilean family, a french fa

12、mily, a british and a canadian familycheng jb. j clin endocr metab 2003, 88:1833对临床的意义对临床的意义 将将pfic和和bric区分出不同的类型区分出不同的类型 diarrhea, pancreatitis （pfic1) 胆石症胆石症 （pfic2) 将将pfic和和bric有机的联系在一起有机的联系在一起 疾病的两极，表型可转换疾病的两极，表型可转换 van ooteghem na, j hepatol 2002,36,439 预后判断预后判断 more progressive in bsep maligna

13、ncy in bsep growth retardation in fic1对临床的意义对临床的意义 histology pfic1：cholestasis with nonspecific hepatitis, low expression of ggt at canalicular pfic2：neonatal hepatitis （multinuclear giant cell transformation) bile acid synthetic defect: giant cell hepatitis chen hl, j pediatr. 2002,140,119 knisely

14、as. perspect pediatr pathol 2000,3,113 bove ke. pediatr dev pathol 2004,7,315对临床的意义对临床的意义 treatment exogenous bile acid administration cure for some bile acid synthetic defect transplatation cure the disease in bsep outside liver symptoms continue(fic1) partial bile diversion d482g or e297g respond

15、well in bsep“transit”neonatal hepatitis the remaining 103 infants were included for analysis. median age at presentation was 40 days (range 7 - 87 days) follow up period ranged between 315 days to 9.6 years, with a median of 873 days there were no patient deaths根据入院时ggt分组，组织学表现有区别wang js, eur j pedi

16、atr, 2006, in pressggt levels rise as bilirubin & ast levels fall. there is a wide variation in time intervals to peak and resolution of disease. this patient presented on day 10 and disease resolved by day 151.typical biochemistry dynamic profile in “transit”patientsbiochemistry dynamic profile

17、 of patient presenting earlypresented on day 3 with a ggt 387 iu/l and cb 83mol/lggt fell to 71 iu/l on day 46 as the ast levels rosea second peak of ggt on day 169 as the bilirubin & ast levels fell.children with idiopathic neonatal hepatitis have more severe disease if their presenting ggt lev

18、els are 100 iu/lhowever, the outcome appears to be good if the ggt becomes raised at a later point of diseasefurther research is required to elucidate the cause of low ggt levels and establish the possible etiologies of idiopathic neonatal hepatitis.bsep gene deletion in a “transit” neonatal hepatitis 图2预后不良患儿例7的生化参数0501001502002503003504004502003.12.252004.1.202004.4.92004.4.122004.4.142004.4.192004.4.162004.5.32004.5.13随访时间gt(u/l)和tb(umol/l)050100150200250300350400450alt(u/l)gttbalt病初曾有血清tb下降