Losa Marco, Scavini Marina, Gatti Elisa, Rossini Alessandro, Madaschi Sara, Formenti Ilaria, Caumo Andrea, Stidley Christine A, Lanzi Roberto
Department of Neurosurgery, Istituto Scientifico San Raffaele, Università Vita-Salute, Milan, Italy.
Thyroid. 2008 Dec;18(12):1249-54. doi: 10.1089/thy.2008.0266.
Clinical studies on the effect of growth hormone (GH) on thyroid function in patients with GH deficiency are contradictory. Further, the majority of published observations are limited to the first 6-12 months of GH replacement therapy. The aim of our study was to estimate the incidence of clinically relevant hypothyroidism in a cohort of patients with adult GH deficiency (AGHD) during long-term therapy with recombinant human GH (rhGH).
The study was designed as a retrospective collection of data on thyroid function in 49 AGHD patients of whom 44 (90%) had multiple hormone deficiency. Thirty-seven patients (76%) were on stable levothyroxine (LT4) replacement therapy (HYPO), and 12 (24%) were euthyroid (EUT). Therapy with rhGH was started at a dose of 3.5 microg/kg body weight and adjusted according to insulin-like growth factor-I (IGF-I) levels. At baseline, 6 months, 12 months, and yearly thereafter we measured free triiodothyronine (fT3), free thyroxine (fT4), thyroid-stimulating hormone, and IGF-I. Study outcome was fT4 level below the normal range (9 pmol/L), irrespectively of fT3 or thyroid-stimulating hormone levels.
During a follow-up of 115 patient-years, mean fT4 level decreased significantly, although remaining within the normal range (p = 0.0242; month 48 vs. baseline). The largest decrease was between baseline and month 6, when fT4 decreased of 1.43 pmol/L (95% confidence interval, 0.33-2.53) per 1 unit (microg/kg body weight) increase in rhGH dose. The incidence of hypothyroidism was 1.2 (HYPO group) and 6.7 (EUT group) events per 100 patient-years.
We confirm that in patients with AGHD, rhGH therapy is associated with a small, although significant, decrement of fT4 in the first 6 months of replacement therapy. However, the incidence of hypothyroidism is low. Monitoring of thyroid function during rhGH therapy is advisable, particularly in the first year of therapy when the largest decrease in fT4 occurs.
关于生长激素(GH)对生长激素缺乏患者甲状腺功能影响的临床研究结果相互矛盾。此外,大多数已发表的观察结果仅限于生长激素替代治疗的前6至12个月。我们研究的目的是评估一组成年生长激素缺乏(AGHD)患者在接受重组人生长激素(rhGH)长期治疗期间临床相关甲状腺功能减退的发生率。
本研究设计为对49例AGHD患者的甲状腺功能数据进行回顾性收集,其中44例(90%)存在多种激素缺乏。37例患者(76%)接受稳定的左甲状腺素(LT4)替代治疗(HYPO组),12例(24%)甲状腺功能正常(EUT组)。rhGH治疗起始剂量为3.5μg/kg体重,并根据胰岛素样生长因子-I(IGF-I)水平进行调整。在基线、6个月、12个月及之后每年,我们测量游离三碘甲状腺原氨酸(fT3)、游离甲状腺素(fT4)、促甲状腺激素和IGF-I。研究结局为fT4水平低于正常范围(9pmol/L),无论fT3或促甲状腺激素水平如何。
在115患者年的随访期间,平均fT4水平虽仍在正常范围内但显著下降(p = 0.0242;第48个月与基线相比)。最大降幅出现在基线至第6个月之间,rhGH剂量每增加1单位(μg/kg体重),fT4下降1.43pmol/L(95%置信区间,0.33 - 2.53)。甲状腺功能减退的发生率为每100患者年1.2次(HYPO组)和6.7次(EUT组)。
我们证实,对于AGHD患者,rhGH治疗在替代治疗的前6个月与fT4虽有小幅但显著的下降有关。然而,甲状腺功能减退的发生率较低。在rhGH治疗期间建议监测甲状腺功能,尤其是在治疗的第一年,此时fT4下降幅度最大。