Prevalence of Metabolic Syndrome in Adult Hypopituitary Growth Hormone (GH)-Deficient Patients Before and After GH Replacement

被引:89
作者
Attanasio, Andrea F. [2 ]
Mo, Daojun [3 ]
Erfurth, Eva Marie [4 ]
Tan, Meng [3 ]
Ho, Ken Y. [5 ]
Kleinberg, David [6 ]
Zimmermann, Alan G. [3 ]
Chanson, Philippe [1 ,7 ,8 ]
机构
[1] Hop Bicetre, AP HP, Ctr Reference Malad Rares Croissance, Serv Endocrinol & Malad Reprod, F-94275 Le Kremlin Bicetre, France
[2] Cascina Rosone, I-14041 Agliano Terme, Italy
[3] Eli Lilly & Co, Lilly Res Labs, Indianapolis, IN 46285 USA
[4] Univ Lund Hosp, Dept Endocrinol, SE-22185 Lund, Sweden
[5] Garvan Inst Med Res, Pituitary Res Unit, Sydney, NSW 2010, Australia
[6] NYU, Sch Med, Neuroendocrine Unit, New York, NY 10016 USA
[7] Univ Paris 11, F-94276 Le Kremlin Bicetre, France
[8] INSERM, Unite 693, F-94276 Le Kremlin Bicetre, France
关键词
CARDIOVASCULAR RISK MARKERS; DEFICIENT ADULTS; INSULIN SENSITIVITY; BODY-COMPOSITION; PREMATURE MORTALITY; DISEASE; ASSOCIATION; PERSISTENCE; DIAGNOSIS; THERAPY;
D O I
10.1210/jc.2009-1326
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Context and Objective: Metabolic and body compositional consequences of GH deficiency (GHD) in adults are associated with a phenotype similar to the metabolic syndrome (MetS). Patients: We assessed MetS prevalence in adult GHD patients (n = 2531) enrolled in the Hypopituitary Control and Complications Study. Prevalence was assessed at baseline and after 3 yr of GH replacement in a subset of 346 adult-onset patients. Results: Baseline MetS crude prevalence was 42.3%; age-adjusted prevalence in the United States and Europe was 51.8 and 28.6% (P < 0.001), respectively. In the United States, age-adjusted prevalence was significantly higher (P < 0.001) than in a general population survey. Increased MetS risk at baseline was observed for age 40 yr or older (adjusted relative risk 1.34, 95% confidence interval 1.17-1.53, P < 0.001), females (1.15, 1.05-1.25, P = 0.002), and adult onset (1.77, 1.44-2.18, P < 0.001). In GH-treated adult-onset patients, MetS prevalence was not changed after 3 yr (42.5-45.7%, P = 0.172), but significant changes were seen for waist circumference (62.1-56.9%, P = 0.008), fasting glucose (26.0-32.4%, P < 0.001), and blood pressure (59.8-69.7%, P < 0.001). Significantly increased risk of MetS at yr 3 was associated with baseline MetS (adjusted relative risk 4.09, 95% confidence interval 3.02-5.53, P < 0.001) and body mass index 30 kg/m(2) or greater (1.53, 1.17-1.99, P = 0.002) and increased risk (with a P value < 0.1) for GH dose 600 mu g/d or greater (1.18, 95% confidence interval 0.98-1.44, P = 0.088). Conclusion: MetS prevalence in GHD patients was higher than in the general population in the United States and higher in the United States than Europe. Prevalence was unaffected by GH replacement, but baseline MetS status and obesity were strong predictors of MetS after GH treatment. (J Clin Endocrinol Metab 95: 74-81, 2010)
引用
收藏
页码:74 / 81
页数:8
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