Chair of Endocrinology, 2nd Faculty of Medicine, University of Rome La Sapienza, via di Grottarossa 1035, 00189 Rome, Italy.
J Endocrinol Invest. 2010 Sep;33(8):534-8. doi: 10.1007/BF03346643. Epub 2010 Feb 15.
Dysfunction of GH-IGF-I axis has been described in many patients affected by β-thalassemia major (TM), especially in children and in adolescents. Recent studies have demonstrated the necessity to evaluate adult patients affected by TM to establish the presence of this alteration which could be relevant in the pathogenesis of cardiac and bone disease, frequently present in this hematological condition. The pathogenesis of this alteration, correlated in the past with iron overload, is not yet completely understood.
The aim of this paper is to evaluate GH-IGF-I axis in a group of adult polytransfused β-thalassemic patients (TM) and to correlate the results with transfusional and chelation parameters.
We performed an arginine plus GHRH stimulation test in 28 adult TM patients. Ferritin, IGF-I, liver enzymes, and liver iron concentration, assessed by a superconducting quantum interference device (SQUID) susceptometer were also determined. Moreover, in each patient we evaluated the bone status by a dual-energy X-ray absorptiometry study.
We found the presence of GH deficit in 9 patients (32.1%). There were no significant differences between the two groups regarding the value of ferritin, liver enzymes, and liver iron concentration, assessed by SQUID. The group affected by GH deficit showed a worse bone profile.
This study confirms the necessity to screen the status of GH/IGF-I axis in this group of patients, even in adult age. The presence of GH deficiency does not seem to be correlated with the efficacy parameters of transfusional and chelation therapy. Other mechanisms, additional to iron overload, could therefore play a role in the pathogenesis of this clinical condition. The presence of GH deficit seems to be very important on clinical aspects, like bone disease, that are crucial for quality of life in these patients.
生长激素-胰岛素样生长因子 I 轴功能障碍已在许多患有重型β地中海贫血(TM)的患者中描述,尤其是在儿童和青少年中。最近的研究表明,有必要评估患有 TM 的成年患者以确定这种改变的存在,这种改变可能与心脏和骨骼疾病的发病机制有关,而这些疾病在这种血液疾病中经常出现。这种改变的发病机制过去与铁过载有关,但尚未完全了解。
本文旨在评估一组成年多输血β地中海贫血患者(TM)的 GH-IGF-I 轴,并将结果与输血和螯合参数相关联。
我们对 28 例成年 TM 患者进行了精氨酸加 GHRH 刺激试验。还测定了铁蛋白、IGF-I、肝酶和肝脏铁浓度,通过超导量子干涉仪(SQUID)磁强计评估。此外,我们在每位患者中通过双能 X 射线吸收仪研究评估了骨骼状况。
我们发现 9 例(32.1%)患者存在 GH 缺乏。两组之间的铁蛋白、肝酶和肝脏铁浓度(通过 SQUID 评估)值无显著差异。GH 缺乏组的骨骼状况较差。
本研究证实了在该组患者中筛查 GH/IGF-I 轴状态的必要性,即使在成年期也是如此。GH 缺乏的存在似乎与输血和螯合治疗的疗效参数无关。因此,除铁过载外,其他机制可能在这种临床疾病的发病机制中起作用。GH 缺乏的存在在骨骼疾病等临床方面非常重要,这些疾病对患者的生活质量至关重要。