Evidence map›Paper›PMID 39463893›Full record

ArticleFrontiers in toxicology2024

Reproductive toxicology: keeping up with our changing world.

Laura B Miller, Morgan B Feuz, Ralph G Meyer, Mirella L Meyer-Ficca

Abstract read
In one paragraph

Article in Frontiers in toxicology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Article
  2. 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

4 authors.

Laura B Miller *Department of Veterinary, Clinical and Life Sciences, College of Veterinary Medicine, Utah State University, Logan, UT, United States.
Morgan B Feuz *Department of Veterinary, Clinical and Life Sciences, College of Veterinary Medicine, Utah State University, Logan, UT, United States.
Ralph G MeyerDepartment of Veterinary, Clinical and Life Sciences, College of Veterinary Medicine, Utah State University, Logan, UT, United States.
Mirella L Meyer-FiccaDepartment of Veterinary, Clinical and Life Sciences, College of Veterinary Medicine, Utah State University, Logan, UT, United States.

Funding

Molecular sensors for metabolic programming of the sperm epigenome and offspring physiologyR01HD103027 · NICHD · UTAH STATE UNIVERSITY · PI MEYER-FICCA, MIRELLA L · 2021 to 2025
$1.5M
NAD Metabolism in Male Reproductive AgingR56AG069745 · NIA · UTAH STATE UNIVERSITY · PI CHINI, EDUARDO N, MEYER-FICCA, MIRELLA L · 2020 to 2020
$381k
Vitamin B3 requirements of the TestisR15HD100970 · NICHD · UTAH STATE UNIVERSITY · PI MEYER, RALPH G · 2020 to 2020
$363k
NIA NIH HHS R56 AG069745NICHD NIH HHS R01 HD103027NICHD NIH HHS R15 HD100970
6 · The paper itself

Abstract

Reproductive toxicology testing is essential to safeguard public health of current and future generations. Traditional toxicological testing of male reproduction has focused on evaluating substances for acute toxicity to the reproductive system, with fertility assessment as a main endpoint and infertility a main adverse outcome. Newer studies in the last few decades have significantly widened our understanding of what represents an adverse event in reproductive toxicology, and thus changed our perspective of what constitutes a reproductive toxicant, such as endocrine disrupting chemicals that affect fertility and offspring health in an intergenerational manner. Besides infertility or congenital abnormalities, adverse outcomes can present as increased likelihood for various health problems in offspring, including metabolic syndrome, neurodevelopmental problems like autism and increased cancer predisposition, among others. To enable toxicologic studies to accurately represent the population, toxicologic testing designs need to model changing population characteristics and exposure circumstances. Current trends of increasing importance in human reproduction include increased paternal age, with an associated decline of nicotinamide adenine dinucleotide (NAD), and a higher prevalence of obesity, both of which are factors that toxicological testing study design should account for. In this perspective article, we highlighted some limitations of standard testing protocols, the need for expanding the assessed reproductive endpoint by including genetic and epigenetic sperm parameters, and the potential of recent developments, including mixture testing, novel animal models,

Indexed as

agingendocrine disrupting chemicalsinfertilityintergenerationalmale reproductionnicotinamide adenine dinucleotideobesityreproductive toxicology

Identifiers

PMID39463893
PMCPMC11502475

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.