The Journal of Clinical Endocrinology & Metabolism · 1991 · 676 citations · 48 references
Life SciencesEndocrinologyPhysiologyAgingHuman NutritionMetabolic RegulationAge-related Physiologic ChangesAge-related Physiological ChangesAging PhysiologyGrowth HormoneGrowth Hormone RegulationPituitary HormonesAge-related Endocrine ChangeAging Male EndocrinologyDeconvolutionGrowth Hormone Age-related ChangesGrowth Hormone MeasurementHormonal Aging EffectsHormonal Changes In AgingPituitary Aging
Mean plasma GH levels depend on burst frequency, amplitude, duration, and endogenous GH half‑life. The study examined how age and adiposity specifically reduce mean serum GH concentrations. Twenty‑one healthy men (21–71 yr) had 24‑h blood sampling every 10 min, and deconvolution analysis quantified GH secretion and clearance parameters. Older age and higher BMI independently lowered GH burst frequency, half‑life, amplitude, and daily secretion, with each decade of age reducing production by 14 % and half‑life by 6 %, and each BMI unit decreasing daily rate by 6 %, together accounting for over 60 % of 24‑h GH production variability.
Mean plasma GH concentrations are controlled by the frequency, amplitude, and duration of underlying GH secretory bursts as well as by the half-life of endogenous GH. We investigated the specific mechanisms that subserve the clinically recognized negative effects of age and adiposity on mean serum GH concentrations. To this end, 21 healthy men, aged 21-71 yr, who were of nearly normal body weight underwent blood sampling at 10-min intervals for 24 h. Deconvolution analysis was used to estimate specific features of GH secretion and clearance. Compared to younger men, the older tertile of men had significant reductions in 1) GH secretory burst frequency, 2) the half-life of endogenous GH, and 3) the daily GH secretory rate, but not 4) GH secretory burst half-duration, amplitude, or mass. Linear regression analysis disclosed that age was a major negative statistical determinant of GH secretory burst frequency (r = -0.80; P = 0.005) and endogenous GH half-life (r = -0.70; P = 0.024). Body mass index, an indicator of relative obesity, was a significant negative correlate of GH half-life (P = 0.045) and GH secretory burst amplitude (P = 0.031). Age and body mass index each correlated negatively with the daily GH secretion rate (P = 0.0031 and P = 0.027, respectively), and together accounted for more than 60% of the variability in 24-h GH production rates (r = -0.78; P = 0.00056). On the average, for a normal body mass index, each decade of increasing age attenuated the GH production rate by 14% and the GH half-life by 6%. Conversely, each unit increase in body mass index, at a given age, reduced the daily GH secretion rate by 6%. We conclude that age and relative adiposity are distinct and specific correlates of individual attributes of GH secretion and clearance in men.
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Effects of Human Growth Hormone in Men over 60 Years Old
Daniel Rudman, Axel G. Feller, Hoskote S. Nagraj et al. · New England Journal of Medicine · 1990 · 1.6K citations · Full text
K. Ho, William S. Evans, Robert M. Blizzard et al. · The Journal of Clinical Endocrinology & Metabolism · 1987 · 928 citations