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Randomized Controlled Trial
. 2010 Jan;95(1):280-8.
doi: 10.1210/jc.2009-1346. Epub 2009 Oct 30.

Cognition is not modified by large but temporary changes in sex hormones in men

Affiliations
Randomized Controlled Trial

Cognition is not modified by large but temporary changes in sex hormones in men

Laura A Young et al. J Clin Endocrinol Metab. 2010 Jan.

Abstract

Context: Little is known about the role of testosterone and estradiol on cognition in healthy older men.

Objective: The cognitive effects of increasing or lowering testosterone or estradiol were examined.

Design: Cognition was assessed before and after 6 wk of double-blind placebo-controlled hormone modification.

Setting: The study was conducted at an academic medical center.

Participants: Healthy older (ages 60-80 yr) and younger men (ages 25-35 yr) were recruited from the community.

Intervention: Men were randomized to one of four treatments: 1) maintain testosterone and estradiol at eugonadal levels for young men (GnRH agonist + testosterone gel); 2) block testosterone's conversion to estradiol (GnRH agonist + testosterone gel + aromatase inhibitor); 3) induce hypogonadism (GnRH agonist alone); and 4) all placebo.

Main outcome measures: Measures of executive function, memory, and spatial cognition were obtained before and after treatment. Hormone levels were obtained 10 times over the course of the study.

Results: Counter to expectations, hormone treatment did not affect cognition (P > 0.10). Free testosterone was positively related to spatial cognition in older men after treatment and controlling for age and estradiol level or exclusion of the hypogonadal men (P = 0.02). Estradiol was negatively associated with working memory controlling for the same variables (P = 0.01). Blinding to treatment assignment was maintained, with the exception of the hypogonadal group.

Conclusions: A significant change in sex hormone status, including complete hypogonadism, does not modify cognition in men. These findings, along with studies that show a risk for neurodegenerative disease in those with low testosterone, suggest that sex hormone status may be important for neuroprotection in aging but not modulation of normal day-to-day cognitive function.

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Figures

Figure 1
Figure 1
Time course of average free testosterone (A) and estradiol (B) levels. Older men are shown in solid lines and younger men in dotted lines. Black arrows depict the timing of the lupron shots. Cognitive testing occurred on the second (V2, pretreatment) and ninth (V9 posttreatment) study visits. The intervals among study visits varied based on the goal of the study visit, and the irregular intervals are delineated by slash marks on the x-axis. V1–V2 was the time between screening and the first study and averaged 20.7 d (sd 14.9), V3 was 4.0 (sd 1.1.) d later to monitor the effects of medication, V4 completed the first study week (4.2 d; 1.9 sd from V3) and was followed by weekly study visits to obtain hormone levels and monitor health thereafter (V5, 6, 7, 8, and 9). This was followed by a safety visit (V10) to ensure that testosterone levels had returned to prestudy, normal values, and the V10 visit was repeated if normal levels were not obtained. The time from V9 to V10 visit that yielded normal levels was 51.1 d (sd 18.6).
Figure 2
Figure 2
Pre- and posttreatment free testosterone (A) and estradiol (B) levels for each group at each age. Error bars are sem.
Figure 3
Figure 3
A, Higher free testosterone is associated with better mental rotation performance in older men (P < 0.05). B, Lower estradiol is associated with better cognitive flexibility (Trails B-A) performance in older men (P < 0.05). Lower score denotes better (faster) performance.

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