Evidence map›Paper›PMID 30032199›Full record

ArticleThe Journal of clinical endocrinology and metabolism2018

Large-for-Gestational-Age May Be Associated With Lower Fetal Insulin Sensitivity and β-Cell Function Linked to Leptin.

Yu Dong, Zhong-Cheng Luo, Anne Monique Nuyt, Francois Audibert, Shu-Qin Wei, Haim A Abenhaim, Emmanuel Bujold, Pierre Julien, Hong Huang, Emile Levy and 2 more

Registry-linked trialOpen access · bronzeAbstract read
In one paragraph

Article in The Journal of clinical endocrinology and metabolism, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03113331 (3D Cohort Study), which is not on this map. Cited by 16 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 1 pooled it
3.6field-weighted citation impact, top 7% 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.

NCT03113331 active not recruitingnot on this map

3D Cohort Study: The Integrated Research Network in Perinatology of Quebec and Eastern Ontario

TypeobservationalSponsorUniversité de SherbrookeRan2010 to 2028Enrolled2,366ConditionsPregnancy Outcome
3 · Its place in the literature

Who cites it

16 citing papers in PubMed, 1 synthesis or guideline pooled it, 23 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Observational
  4. Molecular pathways in placental-fetal development and disruption.Molecular and cellular endocrinology · 2024
    Review
  5. Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Review
  12. Observational
  13. Article
  14. Article
  15. Review
  16. 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

12 authors at 7 institutions in 2 countries.

Yu DongMinistry of Education-Shanghai Key Laboratory of Children's Environmental Health, Pediatric Nephrology, Xinhua Hospital, Shanghai Jiao-Tong University School of Medicine, Shanghai, China.
Zhong-Cheng LuoMinistry of Education-Shanghai Key Laboratory of Children's Environmental Health, Pediatric Nephrology, Xinhua Hospital, Shanghai Jiao-Tong University School of Medicine, Shanghai, China.
Anne Monique NuytSainte-Justine Hospital Research Center, University of Montreal, Montreal, Quebec, Canada.
Francois AudibertSainte-Justine Hospital Research Center, University of Montreal, Montreal, Quebec, Canada.
Shu-Qin WeiSainte-Justine Hospital Research Center, University of Montreal, Montreal, Quebec, Canada.
Haim A AbenhaimJewish General Hospital, McGill University Health Centre, Montreal, Quebec, Canada.
Emmanuel BujoldCHU-Quebec Laval University Research Center, Laval University, Quebec City, Quebec, Canada.
Pierre JulienCHU-Quebec Laval University Research Center, Laval University, Quebec City, Quebec, Canada.
Hong HuangMinistry of Education-Shanghai Key Laboratory of Children's Environmental Health, Pediatric Nephrology, Xinhua Hospital, Shanghai Jiao-Tong University School of Medicine, Shanghai, China.
Emile LevySainte-Justine Hospital Research Center, University of Montreal, Montreal, Quebec, Canada.
William D FraserSainte-Justine Hospital Research Center, University of Montreal, Montreal, Quebec, Canada.
3D Cohort Study Group
Centre Hospitalier Universitaire Sainte-Justine · CAUniversité de Montréal · CAUniversité Laval · CAJewish General Hospital · CAMount Sinai Hospital · CAShanghai Jiao Tong University · CNUniversity of Toronto · CA

Funding

CIHR 151517CIHR 158616CIHR 88413
6 · The paper itself

Abstract

Context: Fetal overgrowth is associated with increased risk for type 2 diabetes in adulthood. It is unclear whether there are alterations in insulin sensitivity and β-cell function in early life. Objective: To determine whether large-for-gestational-age (LGA) (birth weight > 90th percentile), an indicator of fetal overgrowth, is associated with altered fetal insulin sensitivity and β-cell function. Study Design, Population, and Outcomes: In the Design, Development, and Discover birth cohort in Canada, we studied 106 pairs of LGA and optimal-for-gestational-age (OGA; birth weight, 25th to 75th percentiles) infants matched by maternal ethnicity, smoking status, and gestational age. Cord plasma glucose-to-insulin ratio was used as an indicator of fetal insulin sensitivity, and proinsulin-to-insulin ratio was used as an indicator of β-cell function. Cord plasma leptin and high-molecular-weight (HMW) adiponectin concentrations were measured. Results: Comparisons of infants who were born LGA vs OGA, adjusted for maternal and newborn characteristics, showed that cord blood insulin, proinsulin, and leptin concentrations were significantly higher, whereas HWM adiponectin concentrations were similar. Glucose-to-insulin ratios were significantly lower (15.4 ± 28.1 vs 22.0 ± 24.9; P = 0.004), and proinsulin-to-insulin ratios significantly higher (0.73 ± 0.82 vs 0.60 ± 0.78; P = 0.005) in LGA vs OGA newborns, indicating lower insulin sensitivity and β-cell function in LGA newborns. These significant differences were almost unchanged after further adjustment for cord blood adiponectin levels but disappeared upon additional adjustment for cord blood leptin levels. Conclusions: This study demonstrates that LGA may be associated with decreases in both fetal insulin sensitivity and β-cell function. The alterations appear to be linked to elevated leptin levels.

Indexed as

AdiponectinAdultBirth WeightBlood GlucoseCase-Control StudiesFemaleFetal BloodFetal DevelopmentGestational AgeHumansInfant, NewbornInsulin ResistanceInsulin-Secreting CellsLeptinPregnancyAdiponectinADIPOQ protein, humanBlood GlucoseLEP protein, humanLeptin

Identifiers

PMID30032199
PMCPMC6179169
OpenAlexW2883082298

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.