Ubels Froukje L, Rake Jan Peter, Slaets Joris P J, Smit G Peter A, Smit Andries J
Department of Internal Medicine, University Hospital Groningen, PO Box 30001, 9700 RB Groningen, The Netherlands.
Eur J Pediatr. 2002 Oct;161 Suppl 1:S62-4. doi: 10.1007/s00431-002-1006-9. Epub 2002 Jul 2.
Deficiency of microsomal glucose-6-phosphatase in liver and kidney leads to glycogen storage disease type 1a (GSD 1a). Notwithstanding intensive dietary therapy, moderate to severe dyslipidaemia and microalbuminuria, both known atherosclerotic risk factors, remain present. Although more patients reach adult age, no information is still available about accelerated atherosclerosis. The aim of our study was to investigate whether GSD 1a was associated with premature atherosclerosis. In nine adolescent patients (mean age 22.7+/-3.4 years) and nine matched healthy control subjects, lipid profile, blood pressure, ankle-brachial indices, aortic distensibility and intima-media thickness (IMT) of the carotid and femoral arteries were determined. As expected, lipid profiles were significantly unfavourable in the patient group compared with the control group. No differences were found in blood pressure, ankle-brachial indices and aortic distensibility between both groups. IMT segments were comparable in both groups, with even thinner segments in the patient group. In different multivariate models, GSD 1a remained an independent predictor for a thinner IMT (R(2)=0.90; beta=-0.69; P=0.018).
glycogen storage disease type 1a is not associated with premature atherosclerosis, despite the existence of longstanding dyslipidaemia and microalbuminuria.
肝脏和肾脏中微粒体葡萄糖-6-磷酸酶缺乏会导致1a型糖原贮积病(GSD 1a)。尽管进行了强化饮食治疗,但中度至重度血脂异常和微量白蛋白尿这两种已知的动脉粥样硬化危险因素仍然存在。虽然更多患者已成年,但关于动脉粥样硬化加速进展的信息仍然缺乏。我们研究的目的是调查GSD 1a是否与过早动脉粥样硬化有关。对9名青少年患者(平均年龄22.7±3.4岁)和9名匹配的健康对照者测定了血脂谱、血压、踝臂指数、主动脉可扩张性以及颈动脉和股动脉的内膜中层厚度(IMT)。正如预期的那样,与对照组相比,患者组的血脂谱明显不利。两组之间在血压、踝臂指数和主动脉可扩张性方面未发现差异。两组的IMT节段具有可比性,患者组的节段甚至更薄。在不同的多变量模型中,GSD 1a仍然是IMT更薄的独立预测因素(R² = 0.90;β = -0.69;P = 0.018)。
尽管存在长期血脂异常和微量白蛋白尿,但1a型糖原贮积病与过早动脉粥样硬化无关。