Evidence map›Paper›PMID 37592081›Full record

ArticleHandbook of experimental pharmacology2023

Therapeutics for Substance-Using Women: The Need to Elucidate Sex-Specific Targets for Better-Tailored Treatments.

Helen C Fox, Verica Milivojevic, Rajita Sinha

Abstract read
In one paragraph

Article in Handbook of experimental pharmacology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact, top 54% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed, 0 citations in OpenAlex.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors at 2 institutions in 1 country.

Helen C FoxDepartment of Psychiatry and Behavioral Health, Renaissance School of Medicine, Stony Brook University, Stony Brook, NY, USA. Helen.Fox@stonybrookmedicine.edu.
Verica MilivojevicThe Yale Stress Center, Department of Psychiatry, Yale University School of Medicine, New Haven, CT, USA.
Rajita SinhaThe Yale Stress Center, Department of Psychiatry, Yale University School of Medicine, New Haven, CT, USA.
Yale University · USStony Brook School · US

Funding

Guanfacine for women with AUD: A multisite study using a telehealth approachR01AA031662 · NIAAA · INDIANA UNIVERSITY INDIANAPOLIS · PI Helen Cecilia Fox · 2024 to 2026
$2.1M
Cognitive targets for medications development in early abstinent alcoholicsK02AA023566 · NIAAA · STATE UNIVERSITY NEW YORK STONY BROOK · PI FOX, HELEN CECILIA · 2016 to 2020
$643k
Dexamethasone to target stress and immune system changes during early abstinence in individuals with Alcohol Use Disorder (AUD)R21AA029735 · NIAAA · STATE UNIVERSITY NEW YORK STONY BROOK · PI FOX, HELEN CECILIA · 2021 to 2022
$419k
NIAAA NIH HHS K02 AA023566NIAAA NIH HHS R01 AA031662NIAAA NIH HHS R21 AA029735
6 · The paper itself

Abstract

In the last decade, alcohol consumption in the US has risen by 84% in women compared with 35% in men. Furthermore, research has shown that sex- and gender-related differences may disadvantage women in terms of developing a range of psychological, cognitive, and medical problems considerably earlier in their drinking history than men, and despite consuming a similar quantity of substances. While this "telescoping" process has been acknowledged in the literature, a concomitant understanding of the underlying biobehavioral mechanisms, and an increase in the development of specific treatments tailored to women, has not occurred. In the current chapter we focus on understanding why the need for personalized, sex-specific medications is imperative, and highlight some of the potential sex-specific gonadal and stress-related adaptations underpinning the accelerated progress from controlled to compulsive drug and alcohol seeking in women. We additionally discuss the efficacy of these mechanisms as novel targets for medications development, using exogenous progesterone and guanfacine as examples. Finally, we assess some of the challenges faced and progress made in terms of developing innovative medications in women. We suggest that agents such as exogenous progesterone and adrenergic medications, such as guanfacine, may provide some efficacy in terms of attenuating stress-induced craving for several substances, as well as improving the ability to emotionally regulate in the face of stress, preferentially in women. However, to fully leverage the potential of these therapeutics in substance-using women, greater focus needs to the placed on reducing barriers to treatment and research by encouraging women into clinical trials.

Indexed as

GuanfacineProgesteroneAlcohol DrinkingEthanolFemaleHumansMaleEthanolGuanfacineProgesteroneAlcohol useGenderGuanfacineMedication developmentProgesteroneSex-differencesSubstance useWomen

Identifiers

PMID37592081
PMCPMC13045511
OpenAlexW4385934821

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.