Mortality in acromegaly: A 20-year follow-up study

Abstract

Objective: It is unclear whether mortality still is increased in acromegaly and whether there are gender-related differences. We dynamically assessed outcome during long-term follow-up in our nationwide cohort. Patients and methods: We studied standardized mortality ratios (SMRs) relative to the general population and causes of death in acromegaly (n=333) compared with age- and gender-matched controls (n=4995). Results: During 20 (0-33) years follow-up, 113 (34%) patients (n=333, 52%women) and 1334 (27%) controls (n=4995) died (P=0.004). SMR (1.9, 95%CI: 1.53-2.34, P < 0.001) and all-cause mortality (OR 1.6, 95%CI: 1.2-2.2, P < 0.001) were increased in acromegaly. Overall distribution of causes of death (P < 0.001) differed between patients and controls but not cardiovascular (34%vs 33%) or cancer deaths (27%vs 27%). In acromegaly, but not in controls, causes of deaths shifted from 44%cardiovascular and 28%cancer deaths during the first decade, to 23%cardiovascular and 35%cancer deaths during the next two decades. In acromegaly, cancer deaths were mostly attributed to pancreatic adenocarcinoma (n=5), breast (n=4), lung (n=3) and colon (n=3) carcinoma. In acromegaly, men were younger than women at diagnosis (median 44.5 vs 50 years, P < 0.001) and death (67 vs 76 years, P=0.0015). Compared with controls, women (36%vs 25%, P < 0.01), but not men (31%vs 28%, P=0.44), had increased mortality. Conclusions: In acromegaly, men are younger at diagnosis and death than women. Compared with controls, mortality is increased during 20 years of follow-up, especially in women. Causes of deaths shift from predominantly cardiovascular to cancer deaths.