van Varsseveld N C, van Bunderen C C, Franken A A M, Koppeschaar H P F, van der Lely A J, Drent M L
Department of Internal Medicine, Endocrine section, Neuroscience Campus Amsterdam, VU University Medical Center, P.O. Box 7057, 1007 MB, Amsterdam, The Netherlands.
Department of Internal Medicine, Isala Clinics, Zwolle, The Netherlands.
Pituitary. 2016 Aug;19(4):381-90. doi: 10.1007/s11102-016-0716-3.
The effects of growth hormone (GH) replacement therapy on fracture risk in adult GH deficient (GHD) patients with different etiologies of pituitary GHD are not well known, due to limited data. The aim of this study was to investigate characteristics and fracture occurrence at start of (baseline) and during long-term GH replacement therapy in GHD adults previously treated for Cushing's disease (CD) or acromegaly, compared to patients with previous nonfunctioning pituitary adenoma (NFPA).
From the Dutch National Registry of Growth Hormone Treatment in Adults, a nationwide surveillance study in severe GHD adults, all patients using ≥30 days of GH replacement therapy with previous NFPA (n = 783), CD (n = 180) and acromegaly (n = 65) were selected. Patient characteristics, fractures and potential influencing factors were investigated.
At baseline, patients with previous CD were younger, more often female and had more often a history of osteopenia or osteoporosis, whereas patients with previous acromegaly had more often received cranial radiotherapy and a longer duration between treatment of their pituitary tumor and start of adult GH replacement therapy. During follow-up, a fracture occurred in 3.8 % (n = 39) of all patients. Compared to patients with previous NFPA, only patients with previous acromegaly had an increased fracture risk after 6 years of GH replacement therapy.
During GH replacement therapy, an increased fracture risk was observed in severe GHD adult patients previously treated for acromegaly, but not in those previously treated for CD, compared to severe GHD adult patients using GH replacement therapy because of previous NFPA. Further studies are needed to confirm these findings and to elucidate potential underlying mechanisms.
由于数据有限,生长激素(GH)替代疗法对不同病因的成人垂体性生长激素缺乏症(GHD)患者骨折风险的影响尚不清楚。本研究的目的是调查曾接受库欣病(CD)或肢端肥大症治疗的GHD成人患者在开始(基线)和长期GH替代治疗期间的特征及骨折发生情况,并与曾患无功能垂体腺瘤(NFPA)的患者进行比较。
从荷兰全国成人生长激素治疗登记处选取所有使用GH替代疗法≥30天的严重GHD成人患者,这些患者曾患NFPA(n = 783)、CD(n = 180)和肢端肥大症(n = 65)。对患者的特征、骨折情况及潜在影响因素进行调查。
基线时,曾患CD的患者更年轻,女性比例更高,且骨质疏松症或骨质减少症病史更常见;而曾患肢端肥大症的患者接受颅脑放疗的比例更高,垂体肿瘤治疗至成人GH替代治疗开始的间隔时间更长。随访期间,所有患者中有3.8%(n = 39)发生骨折。与曾患NFPA的患者相比,仅曾患肢端肥大症的患者在GH替代治疗6年后骨折风险增加。
在GH替代治疗期间,与因曾患NFPA而接受GH替代治疗的严重GHD成年患者相比,曾接受肢端肥大症治疗的严重GHD成年患者骨折风险增加,而曾接受CD治疗的患者则未出现这种情况。需要进一步研究以证实这些发现并阐明潜在的机制。