Burton Tanya, Le Nestour Elisabeth, Neary Maureen, Ludlam William H
Optum, 950 Winter Street, Waltham, MA, 02451, USA.
InVentiv Health Clinical, 41 rue des 3 fontanot, 92000, Nanterre, France.
Pituitary. 2016 Jun;19(3):262-7. doi: 10.1007/s11102-015-0701-2.
Incidence and prevalence estimates of acromegaly in the United States (US) are limited. Most existing reports are based on European data sources. The objective of this study was to estimate the annual incidence and prevalence of acromegaly in a large US managed care population, overall and stratified by age, sex, and geographic region, using data from 2008 to 2012.
Using administrative claims data, commercial health plan enrollees were identified with acromegaly if they had two or more medical claims with an acromegaly diagnosis code (ICD-9-CM: 253.0×) or one medical claim with an acromegaly diagnosis code in combination with one other claim for a pituitary tumor or pituitary procedure. The first date for an acromegaly-related claim set the index year. Incidence rates for each year were calculated by dividing the number of new acromegaly cases by the calculated person-time at risk. Annual prevalence estimates were calculated by dividing the number with any evidence of acromegaly by the total number of health plan enrollees enrolled for at least 1 day during each calendar year. Incidence and prevalence estimates were stratified by age (0-17, 18-44, 45-64, 65+ years), sex (male, female), and US geographic region of the health plan (Midwest, Northeast, South, West).
Overall annual incidence rates of acromegaly were relatively constant across 2008-2012 with ~11 cases per million person-years (PMPY). Rates increased with age, ranging from 3-8 cases PMPY among children aged 0-17 years old to 9-18 cases PMPY among adults aged 65 and older. Females had 12 cases PMPY on average compared to 10 cases PMPY among men. On average, the Midwest had the lowest incidence rates (7 cases PMPY) compared to the Northeast, South and West (14, 12, and 10 cases PMPY, respectively). The overall annual prevalence of acromegaly was relatively constant across the 5 years from 2008 to 2012 with approximately 78 cases per million each year. Annual prevalence estimates increased with age, ranging from 29-37 cases per million among children aged 0-17 years old to 148-182 cases per million among adults aged 65 years and older. Males and females were similarly affected; each with approximately 77 cases per million each year. The Northeast and South had the highest prevalence estimates (92 and 89 cases per million, respectively); while the estimates for the West and Midwest were lower (65 and 57 cases per million, respectively) each year.
This study examined 5 years of recent data to estimate the incidence and prevalence of acromegaly in a large geographically-diverse managed care population. The incidence rates were higher on average than published rates outside the US (11 vs. 3.3 PMPY), but prevalence estimates were consistent with previous reports. Incidence and prevalence both increased by age, did not differ for males and females, and varied slightly by US geographic region. The age and sex distribution of the selected population matched the known epidemiology of the disease. Using a claims-based approach, this analysis only captured acromegaly cases with an acromegaly-related medical claim. As a result, these estimates may underestimate the incidence and prevalence of acromegaly in US commercial health plans as they did not include individuals who were undiagnosed, in remission, undertreated, or not monitored during the study period. At the same time, these estimates may be viewed as an upper bound on the incidence of acromegaly in the US as the estimates did not include individuals who were in other health plans or uninsured during the study period. Additional evaluations are needed to identify the full extent of acromegaly in the US.
美国肢端肥大症的发病率和患病率估计有限。大多数现有报告基于欧洲数据源。本研究的目的是利用2008年至2012年的数据,估计美国大型管理式医疗人群中肢端肥大症的年发病率和患病率,并按年龄、性别和地理区域进行分层。
利用行政索赔数据,商业健康保险计划参保者若有两条或更多带有肢端肥大症诊断代码(ICD-9-CM:253.0×)的医疗索赔,或一条带有肢端肥大症诊断代码的医疗索赔并伴有另一项垂体肿瘤或垂体手术索赔,则被认定为患有肢端肥大症。与肢端肥大症相关的索赔的首个日期确定为索引年。每年的发病率通过将新的肢端肥大症病例数除以计算出的风险人时来计算。每年的患病率估计值通过将有任何肢端肥大症证据的人数除以每个日历年至少参保1天的健康保险计划参保者总数来计算。发病率和患病率估计值按年龄(0-17岁、18-44岁、45-64岁、65岁及以上)、性别(男性、女性)以及健康保险计划的美国地理区域(中西部、东北部、南部、西部)进行分层。
2008年至2012年期间,肢端肥大症的总体年发病率相对稳定,约为每百万年11例(PMPY)。发病率随年龄增长而增加,0-17岁儿童中为每百万年3-8例,65岁及以上成年人中为每百万年9-18例。女性平均每百万年有12例,男性为每百万年10例。平均而言,中西部地区的发病率最低(每百万年7例),而东北部、南部和西部地区分别为每百万年14例、12例和10例。2008年至2012年的5年中,肢端肥大症的总体年患病率相对稳定,每年约为每百万78例。年患病率估计值随年龄增长而增加,0-17岁儿童中为每百万29-37例,65岁及以上成年人中为每百万148-182例。男性和女性受影响程度相似,每年每百万人均约77例。东北部和南部的患病率估计值最高(分别为每百万92例和89例);而西部和中西部地区每年的估计值较低(分别为每百万65例和57例)。
本研究检查了5年的近期数据,以估计地域广泛的大型管理式医疗人群中肢端肥大症的发病率和患病率。平均发病率高于美国以外公布的发病率(每百万年11例对3.3例),但患病率估计值与先前报告一致。发病率和患病率均随年龄增长而增加,男性和女性无差异,在美国地理区域略有不同。所选人群的年龄和性别分布与该疾病已知的流行病学情况相符。采用基于索赔的方法,该分析仅捕获了有肢端肥大症相关医疗索赔的肢端肥大症病例。因此,这些估计可能低估了美国商业健康保险计划中肢端肥大症的发病率和患病率,因为它们未包括在研究期间未被诊断、处于缓解期、治疗不足或未接受监测的个体。同时,这些估计也可被视为美国肢端肥大症发病率的上限,因为这些估计未包括研究期间参加其他健康保险计划或未参保的个体。需要进行更多评估以确定美国肢端肥大症的全貌。