Search

Nonhuman primate (NHP) studies are crucial to biomedical research. NHPs are the species most similar to humans in lifespan, body size, and hormonal profiles. Planning research requires statistical power evaluation, which is difficult to perform when lacking directly relevant preliminary data. This is especially true for NHP developmental programming studies, which are scarce. We review the sample sizes reported, challenges, areas needing further work, and goals of NHP maternal nutritional programming studies. The literature search included 27 keywords, for example, maternal obesity, intrauterine growth restriction, maternal high-fat diet, and maternal nutrient reduction. Only fetal and postnatal offspring studies involving tissue collection or imaging were included. Twenty-eight studies investigated maternal over-nutrition and 33 under-nutrition; 23 involved macaques and 38 baboons. Analysis by sex was performed in 19; minimum group size ranged from 1 to 8 (mean 4.7 ± 0.52, median 4, mode 3) and maximum group size from 3 to 16 (8.3 ± 0.93, 8, 8). Sexes were pooled in 42 studies; minimum group size ranged from 2 to 16 (mean 5.3 ± 0.35, median 6, mode 6) and maximum group size from 4 to 26 (10.2 ± 0.92, 8, 8). A typical study with sex-based analyses had group size minimum 4 and maximum 8 per sex. Among studies with sexes pooled, minimum group size averaged 6 and maximum 8. All studies reported some significant differences between groups. Therefore, studies with group sizes 3–8 can detect significance between groups. To address deficiencies in the literature, goals include increasing age range, more frequently considering sex as a biological variable, expanding topics, replicating studies, exploring intergenerational effects, and examining interventions. [ABSTRACT FROM AUTHOR]

Background: Non‐human primate models of developmental programing by maternal mismatch between pregnancy and lactation diets are needed for translation to human programing outcomes. We present baboon offspring morphometry from birth to 3 years, and blood cortisol and adrenocorticotropin (ACTH) from 2 to 24 months. Methods: Control mothers ate chow; mismatch mothers ate 30% less than controls during pregnancy and high‐fat high‐energy diet through lactation. Results: Mismatch mothers lost weight during pregnancy. At birth, there were trends toward lower weight in mismatch offspring of both sexes (P = 0.06). From 0‐3 years, catch‐up growth occurred. Mismatch offspring male and female body weight increased faster than controls (P < 0.001). Mismatch female offspring showed greater increase in BMI (P < 0.001) and abdominal circumference (P = 0.008) vs controls. ACTH and cortisol slopes from 2 to 24 months of age were similar between groups in both sexes. Cortisol and ACTH increased after weaning in all groups. Conclusions: Mismatch produces sexually dimorphic post‐natal growth phenotypes. [ABSTRACT FROM AUTHOR]

Background: Non‐human primate models of developmental programming by maternal obesity (MO) are needed for translation to human programming outcomes. We present baboon offspring (F1) morphometry, blood cortisol, and adrenocorticotropic hormone (ACTH) from 0.9 gestation to 0‐2 years. Methods: Control mothers ate chow; MO mothers ate high‐fat high‐energy diet pre‐pregnancy through lactation. Results: Maternal obesity mothers weighed more than controls pre‐pregnancy. Maternal obesity gestational weight gain was lower with no correlation with fetal or placenta weights. At 0.9 gestation, MO and control F1 morphometry and ACTH were similar. MO‐F1 0.9 gestation male cortisol was lower, rising slower from 0‐2 years vs control‐F1. At birth, male MO‐F1 and control‐F1 weights were similar, but growth from 0‐2 years was steeper in MO‐F1; newborn female MO‐F1 weighed more than control‐F1 but growth from 0‐2 years was similar. ACTH did not change in either sex. Conclusions: Maternal obesity produced sexually dimorphic fetal and postnatal growth and hormonal phenotypes. [ABSTRACT FROM AUTHOR]

Background Most developmental programming studies on maternal nutrient reduction ( MNR) are in altricial rodents whose maternal nutritional burden and offspring developmental trajectory differ from precocial non-human primates and humans. Methods Control ( CTR) baboon mothers ate ad libitum; MNR mothers ate 70% global control diet in pregnancy and lactation. Results We present offspring morphometry, blood cortisol, and adrenocorticotropin ( ACTH) during second half of gestation (G) and first three postnatal years. Moderate MNR produced intrauterine growth restriction ( IUGR). IUGR males (n=43) and females (n=28) were smaller than CTR males (n=50) and females (n=47) in many measurements at many ages. In CTR, fetal ACTH increased 228% and cortisol 48% between 0.65G and 0.9G. IUGR ACTH was elevated at 0.65G and cortisol at 0.9G. 0.9G maternal gestational weight gain, fetal weight, and placenta weight were correlated. Conclusions Moderate IUGR decreased body weight and morphometric measurements at key time points and altered hypothalamo-pituitary-adrenal function. [ABSTRACT FROM AUTHOR]

We investigated menstrual cycles in intrauterine growth restricted (IUGR, 7‐10 years, n = 8) and age‐matched control (n = 10) baboons. Cycle duration and plasma anti‐Mullerian hormone were similar. IUGR spent more days per cycle swollen and had elevated early morning fasted serum cortisol, suggesting normal fertility in the presence of increased psychosocial stress. [ABSTRACT FROM AUTHOR]