Evidence map›Paper›PMID 30728429›Full record

ArticleScientific reports2019

Increased adiposity, inflammation, metabolic disruption and dyslipidemia in adult male offspring of DOSS treated C57BL/6 dams.

Alexis M Temkin, Robert R Bowers, Candice Z Ulmer, Kayla Penta, John A Bowden, Jennifer Nyland, John E Baatz, Demetri D Spyropoulos

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
4.7field-weighted citation impact, top 6% 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

14 citing papers in PubMed, 1 synthesis or guideline pooled it, 27 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. Article
  6. Ultra-processed foods and food additives in gut health and disease.Nature reviews. Gastroenterology & hepatology · 2024
    Review
  7. Article
  8. Review
  9. Review
  10. Article
  11. Obesity and endocrine-disrupting chemicals.Endocrine connections · 2021
    Review
  12. The new kids on the block: Emerging obesogens.Advances in pharmacology (San Diego, Calif.) · 2021
    Review
  13. Review
  14. Review
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

8 authors at 5 institutions in 1 country.

Alexis M TemkinMolecular and Cellular Biology and Pathobiology Program, Medical University of South Carolina, Charleston, SC, USA.
Robert R BowersDepartment of Pathology and Laboratory Medicine, Medical University of South Carolina, Charleston, SC, USA.
Candice Z UlmerNational Institute of Standards and Technology, Chemical Sciences Division, Hollings Marine Laboratory, Charleston, SC, USA.
Kayla PentaDepartment of Biological Sciences, University of South Carolina, Columbia, SC, USA.
John A BowdenNational Institute of Standards and Technology, Chemical Sciences Division, Hollings Marine Laboratory, Charleston, SC, USA.
Jennifer NylandDepartment of Biological Sciences, Salisbury University, Salisbury, MD, USA.
John E BaatzDepartment of Pediatrics and Neonatology, Medical University of South Carolina, Charleston, SC, USA.
Demetri D SpyropoulosMolecular and Cellular Biology and Pathobiology Program, Medical University of South Carolina, Charleston, SC, USA. spyropdd@musc.edu.
Medical University of South Carolina · USNational Institute of Standards and Technology · USNCCOS Hollings Marine Laboratory · USSalisbury University · USUniversity of South Carolina · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Evidence indicates that obesity can be promoted by chemical 'obesogens' that drive adiposity, hunger, inflammation and suppress metabolism. Dioctyl sodium sulfosuccinate (DOSS), a lipid emulsifier and candidate obesogen in vitro, is widely used in processed foods, cosmetics and as stool softener medicines commonly used during pregnancy. In vivo testing of DOSS was performed in a developmental origins of adult obesity model. Pregnant mice were orally administered vehicle control or DOSS at times and doses comparable to stool softener use during human pregnancy. All weaned offspring consumed only standard diet. Adult male but not female offspring of DOSS-treated dams showed significantly increased body mass, overall and visceral fat masses, and decreased bone area. They exhibited significant decreases in plasma adiponectin and increases in leptin, glucose intolerance and hyperinsulinemia. Inflammatory IL-6 was elevated, as was adipose Cox2 and Nox4 gene expressions, which may be associated with promoter DNA methylation changes. Multiple significant phospholipid/sterol lipid increases paralleled profiles from long-term high-fat diet induced obesity in males. Collectively, developmental DOSS exposure leads to increased adult adiposity, inflammation, metabolic disorder and dyslipidemia in offspring fed a standard diet, suggesting that pharmaceutical and other sources of DOSS taken during human pregnancy might contribute to long-term obesity-related health concerns in offspring.

Indexed as

AdiposityAnimalsDioctyl Sulfosuccinic AcidDyslipidemiasFemaleGlucose IntoleranceInflammationMaleMetabolic DiseasesMiceMice, Inbred C57BLObesityPregnancyPrenatal Exposure Delayed EffectsSurface-Active AgentsDioctyl Sulfosuccinic AcidSurface-Active Agents

Identifiers

PMID30728429
PMCPMC6365642
OpenAlexW2912707139

What OpenQuestion 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 OpenQuestion graph.