Janus E D, Nicoll A M, Turner P R, Magill P, Lewis B
Eur J Clin Invest. 1980 Apr;10(2 Pt 1):161-72. doi: 10.1111/j.1365-2362.1980.tb02076.x.
Autologous 131I-labelled very low density lipoprotein (VLDL) and 125I-labelled low density lipoprotein (LDL) were injected into seven normal subjects and into forty-three hyperlipidaemic patients, classified into groups on the basis of family studies and clinical findings, to quantitate VLDL and LDL apolipoprotein B kinetics. In normal subjects, mean VLDL-B peptide synthetic rate was 15 . 1 mg kg-1 day-1, mean LDL-B peptide synthetic rate 7 . 7 mg kg-1 day-1 and mean LDL-B fractional catabolic rate (FCR) 0 . 31 day-1. In heterozygous familial hypercholesterolaemia (n = 14) VLDL-B peptide production was normal in patients with normal triglyceride levels; in those with high triglyceride levels there was either VLDL overproduction or a catabolic defect. LDL-B peptide synthetic rates ranged from high normal to increased (8 . 5--18 . 0 mg kg-1 day-1) and LDL-B peptide FCR values were markedly reduced (0 . 14--0 . 28 day-1) confirming the presence of a defect in LDL catabolism but indicating over-production as well. In familial combined hyperlipidaemia (n = 11) VLDL-B peptide production ranged from normal to elevated (13 . 9--44 . 4 mg kg-1 day-1, mean 23 . 8 mg kg-1 day-1) correlating with the VLDl triglyceride level (i.e. with the phenotypic expression of the disorder). LDL-B peptide production ranged from high normal to markedly increased (8 . 9--19 . 5 mg kg-1 day-1, mean 12 . 2 mg kg-1 day-1) and correlated with LDL cholesterol levels (i.e. the phenotype), (r = +0 . 66, P < 0 . 05). Three patients with unclassified hypercholesterolaemia had increased LDL-B peptide synthetic rates. One patient with remnant hyperlipoproteinaemia (type III) had a high normal VLDL-B peptide synthetic rate, 17 . 3 mg kg-1 day-1, and a strikingly low FCR of VLDL-B. In familial hypertriglyceridaemia (three patients) there was a low VLDL-B peptide FCR. In unclassified hypertriglyceridaemia VLDL over-production was the finding in seven patients but four patients appeared to have catabolic defects only. Overall there were significant hyperbolic relationships between VLCL-B peptide FCR and VLDL-B peptide concentration (r = -0 . 78, P < 0 . 001, for the log/log relationship) and between LDL-B peptide FCR and LDL cholesterol (r = -0 . 88, P < 0 . 001 for the log/log relationship.)
将自体131I标记的极低密度脂蛋白(VLDL)和125I标记的低密度脂蛋白(LDL)注入7名正常受试者和43名高脂血症患者体内,这些患者根据家族研究和临床发现进行分组,以定量VLDL和LDL载脂蛋白B的动力学。在正常受试者中,VLDL-B肽的平均合成率为15.1mg·kg-1·天-1,LDL-B肽的平均合成率为7.7mg·kg-1·天-1,LDL-B的平均分解代谢率(FCR)为0.31天-1。在杂合子家族性高胆固醇血症(n = 14)中,甘油三酯水平正常的患者VLDL-B肽产生正常;甘油三酯水平高的患者则存在VLDL产生过多或分解代谢缺陷。LDL-B肽合成率从正常高值到升高(8.5 - 18.0mg·kg-1·天-1),LDL-B肽FCR值明显降低(0.14 - 0.28天-1),这证实了LDL分解代谢存在缺陷,但也表明存在产生过多的情况。在家族性混合性高脂血症(n = 11)中,VLDL-B肽产生率从正常到升高(13.9 - 44.4mg·kg-1·天-1,平均23.8mg·kg-1·天-1),与VLDL甘油三酯水平相关(即与该疾病的表型表达相关)。LDL-B肽产生率从正常高值到明显升高(8.9 - 19.5mg·kg-1·天-1,平均12.2mg·kg-1·天-1),并与LDL胆固醇水平(即表型)相关(r = +0.66,P < 0.05)。3例未分类高胆固醇血症患者的LDL-B肽合成率升高。1例残留性高脂蛋白血症(III型)患者的VLDL-B肽合成率正常高值为17.3mg·kg-1·天-1,VLDL-B的FCR极低。在家族性高甘油三酯血症(3例患者)中,VLDL-B肽FCR较低。在未分类的高甘油三酯血症中,7例患者存在VLDL产生过多,但4例患者似乎仅存在分解代谢缺陷。总体而言,VLCL-B肽FCR与VLDL-B肽浓度之间存在显著的双曲线关系(对数/对数关系,r = -0.78,P < 0.001),LDL-B肽FCR与LDL胆固醇之间也存在显著的双曲线关系(对数/对数关系,r = -0.88,P < 0.001)。