Radian Serban, Diekmann Yoan, Gabrovska Plamena, Holland Brendan, Bradley Lisa, Wallace Helen, Stals Karen, Bussell Anna-Marie, McGurren Karen, Cuesta Martin, Ryan Anthony W, Herincs Maria, Hernández-Ramírez Laura C, Holland Aidan, Samuels Jade, Aflorei Elena Daniela, Barry Sayka, Dénes Judit, Pernicova Ida, Stiles Craig E, Trivellin Giampaolo, McCloskey Ronan, Ajzensztejn Michal, Abid Noina, Akker Scott A, Mercado Moises, Cohen Mark, Thakker Rajesh V, Baldeweg Stephanie, Barkan Ariel, Musat Madalina, Levy Miles, Orme Stephen M, Unterländer Martina, Burger Joachim, Kumar Ajith V, Ellard Sian, McPartlin Joseph, McManus Ross, Linden Gerard J, Atkinson Brew, Balding David J, Agha Amar, Thompson Chris J, Hunter Steven J, Thomas Mark G, Morrison Patrick J, Korbonits Márta
Centre of Endocrinology, William Harvey Research Institute, Barts and the London School of Medicine and Dentistry, Queen Mary University of London, London, UK.
Department of Endocrinology, Carol Davila University of Medicine and Pharmacy, C.I. Parhon National Institute of Endocrinology, Bucharest, Romania.
Hum Mutat. 2017 Jan;38(1):78-85. doi: 10.1002/humu.23121. Epub 2016 Oct 4.
The aryl hydrocarbon receptor interacting protein (AIP) founder mutation R304 (or p.R304 ; NM_003977.3:c.910C>T, p.Arg304Ter) identified in Northern Ireland (NI) predisposes to acromegaly/gigantism; its population health impact remains unexplored. We measured R304 carrier frequency in 936 Mid Ulster, 1,000 Greater Belfast (both in NI) and 2,094 Republic of Ireland (ROI) volunteers and in 116 NI or ROI acromegaly/gigantism patients. Carrier frequencies were 0.0064 in Mid Ulster (95%CI = 0.0027-0.013; P = 0.0005 vs. ROI), 0.001 in Greater Belfast (0.00011-0.0047) and zero in ROI (0-0.0014). R304 prevalence was elevated in acromegaly/gigantism patients in NI (11/87, 12.6%, P < 0.05), but not in ROI (2/29, 6.8%) versus non-Irish patients (0-2.41%). Haploblock conservation supported a common ancestor for all the 18 identified Irish pedigrees (81 carriers, 30 affected). Time to most recent common ancestor (tMRCA) was 2550 (1,275-5,000) years. tMRCA-based simulations predicted 432 (90-5,175) current carriers, including 86 affected (18-1,035) for 20% penetrance. In conclusion, R304 is frequent in Mid Ulster, resulting in numerous acromegaly/gigantism cases. tMRCA is consistent with historical/folklore accounts of Irish giants. Forward simulations predict many undetected carriers; geographically targeted population screening improves asymptomatic carrier identification, complementing clinical testing of patients/relatives. We generated disease awareness locally, necessary for early diagnosis and improved outcomes of AIP-related disease.
在北爱尔兰(NI)发现的芳烃受体相互作用蛋白(AIP)的奠基者突变R304(或p.R304;NM_003977.3:c.910C>T,p.Arg304Ter)易导致肢端肥大症/巨人症;其对人群健康的影响尚待探索。我们检测了936名中阿尔斯特地区、1000名大贝尔法斯特地区(均在NI)以及2094名爱尔兰共和国(ROI)志愿者,以及116名NI或ROI的肢端肥大症/巨人症患者中R304携带者的频率。中阿尔斯特地区的携带者频率为0.0064(95%CI = 0.0027 - 0.013;与ROI相比,P = 0.0005),大贝尔法斯特地区为0.001(0.00011 - 0.0047),ROI为零(0 - 0.0014)。NI的肢端肥大症/巨人症患者中R304的患病率升高(11/87,12.6%,P < 0.05),但ROI的患者中未升高(2/29,6.8%),与非爱尔兰患者(0 - 2.41%)相比。单倍型块保守性支持所有18个已识别的爱尔兰家系(81名携带者,30名患者)有共同祖先。最近共同祖先时间(tMRCA)为2550(1275 - 5000)年。基于tMRCA的模拟预测当前有432名(90 - 5175)携带者,其中20%的外显率下有86名患者(18 - 1035)。总之,R304在中阿尔斯特地区很常见,导致众多肢端肥大症/巨人症病例。tMRCA与爱尔兰巨人的历史/民间传说记载相符。前瞻性模拟预测有许多未被检测到的携带者;地理定位的人群筛查可提高无症状携带者的识别率,补充对患者/亲属的临床检测。我们在当地提高了疾病认知度,这对于AIP相关疾病的早期诊断和改善预后是必要的。