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Santoro, N.

Publications and source records attributed to Santoro, N..

3 recordsLinked to original sources

On modeling ovarian aging and menopause timing

Mathematical modeling of ovarian aging and menopause timing has a long history, dating back a half-century to the models of Nobel Prize winner Robert G. Edwards. More recently, such models have been used to investigate clinical interventions for women, which underscores the importance of scientific rigor in model development and analysis. In this paper, we analyze a recent model published in the biophysics literature. We first correct an error which invalidates claims about menopause age in different populations. We then use stochastic analysis to show how this model is a reparameterization of a prior model and put it in the framework of several prior models, which enables the application of extreme value theory. We prove some general extreme value theory results and use them to obtain detailed estimates of menopause age in this model. In particular, we derive a new expected menopause age formula which is orders of magnitude more accurate than the previous heuristic estimate. We further obtain rigorous analytical estimates of the full menopause age distribution and all its moments. We conclude by using these mathematical results to elucidate the physiological sources of menopause age variability.

physiology↗

Uncovering active modulators of native macroautophagy through novel high-content screens

Autophagy is an evolutionarily conserved pathway mediating the breakdown of cellular proteins and organelles. Emphasizing its pivotal nature, autophagy dysfunction contributes to many diseases; nevertheless, development of effective autophagy modulating drugs is hampered by fundamental deficiencies in available methods for measuring autophagic activity, or flux. To overcome these limitations, we introduced the photoconvertible protein Dendra2 into the MAP1LC3B locus of human cells via CRISPR/Cas9 genome editing, enabling accurate and sensitive assessments of autophagy in living cells by optical pulse labeling. High-content screening of 1,500 tool compounds provided construct validity for the assay and uncovered many new autophagy modulators. In an expanded screen of 24,000 diverse compounds, we identified additional hits with profound effects on autophagy. Further, the autophagy activator NVP-BEZ235 exhibited significant neuroprotective properties in a neurodegenerative disease model. These studies confirm the utility of the Dendra2-LC3 assay, while simultaneously highlighting new autophagy-modulating compounds that display promising therapeutic effects.

cell biology↗

Sex Differences in Effects of Obesity on Reproductive Hormones and Glucose Metabolism in Puberty: The Health Influences of Puberty Study

ContextObesity is known to impact reproductive function in adults, but little is known about its effects on reproductive hormones during puberty or sex differences in these effects.\n\nObjectiveTo assess sex differences in effects of obesity on reproductive hormones and their relationship to insulin sensitivity and secretion.\n\nDesignCross-sectional study including anthropometrics, serum and urine reproductive hormone concentrations, and intravenous glucose tolerance testing (IVGTT) to assess acute insulin response to glucose (AIRg) and insulin sensitivity (Si)\n\nSettingOutpatient academic clinical research center\n\nPatientsFifty-one normal weight (NW, BMI-Z=-0.11 {+/-} 0.77, age=11.5 {+/-} 1.7 years) and 53 obese (BMI-Z=2.22 {+/-} 0.33, age=10.9 {+/-} 1.5 years) girls (n=54) and boys (n=50), Tanner stage 2-3\n\nResultsObese boys had lower total testosterone (p<0.0001) and higher concentrations of the urinary estradiol metabolite, E1c, (p=0.046) than NW boys. Obese girls had higher free androgen index (FAI, p=0.03) than NW girls. Both obese boys and girls had lower sex hormone-binding globulin (SHBG, p<0.0001) than NW. AIRg was inversely related to SHBG in boys (R2= 0.36, p<0.0001) and girls (R2=0.29, p=0.0001). Insulin resistance correlated with lower SHBG in boys (R2=0.45, p<0.0001) and girls (R2=0.24, p=0.0003), lower total testosterone for boys (R2=0.15, p=0.01), and higher FAI for girls (R2=0.08, p=0.04).\n\nConclusionObese youth have lower SHBG than NW youth, but obesity has differential effects on reproductive hormones in girls vs. boys, which are apparent early in puberty. Ongoing longitudinal studies will evaluate the impact of obesity on reproductive hormones in girls and boys as puberty progresses.

physiology↗