de Gennes J L, Turpin G, Heshmati H M, Lebrun A
Nouv Presse Med. 1979 Dec 3;8(47):3877-80.
Twelve cases of hypopituitarism (Sheehan's syndrome, pituitary adenoma, idiopathic) associated with hyperlipidemia (type IIb in general) are reported. It is suggested that: 1 - Growth hormone deficiency seems to have a protective effect against atherosclerosis in hyperlipidemia because there are no cardiovascular signs in 10 cases with a history of growth hormone deficiency lasting from 5 to 57 years and a patent hyperlipidemia (lasting a mean of 23 years), and there is stabilisation or improvement of ischemic signs in 2 other cases. 2 - Lipid abnormalities are frequently seen in hypopituitarism even after thyroid replacement therapy. 3 - The hyperlipidemia can be familial or can result from growth hormone deficiency alone.
报告了12例垂体功能减退症(席汉综合征、垂体腺瘤、特发性)合并高脂血症(一般为IIb型)的病例。研究表明:1 - 生长激素缺乏似乎对高脂血症患者的动脉粥样硬化具有保护作用,因为在10例生长激素缺乏病史持续5至57年且高脂血症持续存在(平均持续23年)的患者中未出现心血管体征,另外2例患者的缺血体征得到稳定或改善。2 - 即使在进行甲状腺替代治疗后,垂体功能减退症患者仍经常出现脂质异常。3 - 高脂血症可能是家族性的,也可能仅由生长激素缺乏引起。