Frontier mental health research: psychedelics & drug studies

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4 papers

Testosterone in Female Depression: A Meta-Analysis and Mendelian Randomization Study

Dhruba Tara Maharjan, Ali Alamdar Shah Syed, Guan Ning Lin, Weihai Ying
Biomolecules Summary & key facts 2021 28 citations

This paper combined past studies (a meta-analysis) and a genetic test (Mendelian randomization) to look at blood testosterone and depression in women. The meta-analysis found that women with depression have significantly different serum testosterone levels than healthy women, with a clear result in premenopausal women and weaker (borderline) results in…

Hormonal and reproductive studies Hypothalamic control of reproductive hormones Stress Responses and Cortisol

Antidepressant Treatment and Manic Switch in Bipolar I Disorder: A Clinical and Molecular Genetic Study

Chih‐Ken Chen, Lawrence Shih-Hsin Wu, Ming‐Chyi Huang, Chian‐Jue Kuo, Andrew T. A. Cheng

Researchers studied 1004 people with bipolar I disorder who had at least one depressive episode. They found that people who received antidepressant treatment were more likely to have a manic episode within eight weeks after their depression got better. A genetic marker (rs10262219) showed a strong signal in the first…

Adolescent and Pediatric Healthcare Bipolar Disorder and Treatment Genetics and Neurodevelopmental Disorders

Panic disorders: The role of genetics and epigenetics

Eun Jeong Kim, Yong‐Ku Kim
AIMS Genetics Summary & key facts 2018 19 citations

This paper reviews studies of genes and epigenetics in panic disorder. Family, twin, and adoption studies show panic disorder often runs in families. Researchers have found some candidate genes (for example NPY, ADORA2A, COMT, IKBKE), but panic disorder is not a single-gene disease. Large genome-wide studies did not find any…

Anxiety, Depression, Psychometrics, Treatment, Cognitive Processes Child and Adolescent Psychosocial and Emotional Development Schizophrenia research and treatment

Hypogonadotropic hypogonadism due to compound heterozygous mutations TACR3 in siblings

Rita Valsassina, Filipa Briosa, Joana Soares, Marta Amorim, Catarina Limbert
Clinical Case Reports Summary & key facts 2020 2 citations

The authors present a new association of two heterozygous TACR3 mutations (p.Arg230His and p.Trp275*) responsible for a clinical trait of normosmic congenital hypogonadotropic hypogonadism in a family.

Biotin and Related Studies Genomics and Chromatin Dynamics Hypothalamic control of reproductive hormones
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