A study of acromegaly-associated headache with somatostatin analgesia.

IF 4.1 2区 医学 Q2 ENDOCRINOLOGY & METABOLISM Endocrine-related cancer Pub Date : 2023-02-16 Print Date: 2023-03-01 DOI:10.1530/ERC-22-0138
Sonia Kaniuka-Jakubowska, Miles J Levy, Aparna Pal, Dayakshi Abeyaratne, William M Drake, Nikolaos Kyriakakis, Robert D Murray, Steve M Orme, Shailesh Gohil, Antonia Brooke, Graham P Leese, Márta Korbonits, John Ah Wass
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Abstract

The aim of this study is to characterise somatostatin analogue-responsive headache in acromegaly, hitherto not systematically documented in a significant cohort. Using the UK pituitary network, we have clinically characterised a cohort of 18 patients suffering from acromegaly-related headache with a clear response to somatostatin analogues. The majority of patients had chronic migraine (78%) as defined by the International Headache Society diagnostic criteria. Headache was present at the time of acromegaly presentation and clearly associated temporally with disease activity in all cases. Short-acting somatostatin analogues uniquely resolved pain within minutes and the mean duration of analgesia was 1-6 h. Patients on long-acting analogues required less short-acting injections (mean: 3.7 vs 10.4 injections per day, P = 0.005). 94% used somatostatin analogues to control ongoing headache pain. All patients presented with macroadenoma, most had incomplete resection (94%) and headache was ipsilateral to remnant tissue (94%). Although biochemical control was achieved in 78% of patients, headache remained in 71% of them. Patients selected for this study had ongoing headache post-treatment (mean duration: 16 years after diagnosis); only four patients reached headache remission 26 years (mean range: 14-33) after the diagnosis. Headache in acromegaly patients can be persistent, severe, unrelieved by surgery, long-lasting and uncoupled from biochemical control. We show here that long-acting analogues allow a decrease in the number of short-acting analogue injections for headache relief. Further studies are needed to understand the mechanisms, markers and tumour tissue characteristics of acromegaly-related headache. Until then, this publication serves to provide the clinical characteristics as a reference point for further study.

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生长抑素镇痛治疗肢端肥大症相关头痛的研究。
本研究的目的是描述肢端肥大症中生长抑素类似物反应性头痛的特征,迄今为止尚未在重要队列中系统记录。使用英国垂体网络,我们对一组18名患有肢端肥大症相关头痛的患者进行了临床表征,这些患者对生长抑素类似物有明显反应。根据国际头痛协会的诊断标准,大多数患者患有慢性偏头痛(78%)。头痛出现在肢端肥大症时,并且在所有病例中都与疾病活动在时间上明显相关。短效生长抑素类似物能在几分钟内独特地缓解疼痛,平均镇痛持续时间为1-6小时。服用长效类似物的患者需要较少的短效注射(平均每天3.7次vs 10.4次,P=0.005)。94%的患者使用生长抑素类似品来控制持续的头痛。所有患者均表现为大腺瘤,大多数切除不全(94%),头痛与残留组织同侧(94%)。尽管78%的患者实现了生化控制,但71%的患者仍然头痛。本研究中选择的患者在治疗后持续头痛(平均持续时间:诊断后16年);只有4名患者在诊断后26年(平均范围:14-33)达到头痛缓解。肢端肥大症患者的头痛可能是持续的、严重的、手术无法缓解的、持久的并且与生化控制无关。我们在这里表明,长效类似物可以减少用于缓解头痛的短效类似物注射的数量。需要进一步的研究来了解肢端肥大症相关头痛的机制、标志物和肿瘤组织特征。在此之前,本出版物旨在提供临床特征,作为进一步研究的参考点。
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来源期刊
Endocrine-related cancer
Endocrine-related cancer 医学-内分泌学与代谢
CiteScore
7.80
自引率
2.60%
发文量
138
审稿时长
6-12 weeks
期刊介绍: Endocrine-Related Cancer is an official flagship journal of the Society for Endocrinology and is endorsed by the European Society of Endocrinology, the United Kingdom and Ireland Neuroendocrine Society, and the Japanese Hormones and Cancer Society. Endocrine-Related Cancer provides a unique international forum for the publication of high quality original articles describing novel, cutting edge basic laboratory, translational and clinical investigations of human health and disease focusing on endocrine neoplasias and hormone-dependent cancers; and for the publication of authoritative review articles in these topics. Endocrine neoplasias include adrenal cortex, breast, multiple endocrine neoplasia, neuroendocrine tumours, ovary, prostate, paraganglioma, parathyroid, pheochromocytoma pituitary, testes, thyroid and hormone-dependent cancers. Neoplasias affecting metabolism and energy production such as bladder, bone, kidney, lung, and head and neck, are also considered.
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