# Serum lncRNA H19/miR-675 /PPARα expression before middle gestation and their associations with macrosomia risk in singleton pregnancies without gestational diabetes mellitus: a preliminary study

**Authors:** Qiuyan Yu, Ming Min Jin, Miao Miao Ding, Bin Wei Cheng, Xiao Xia He, Xin Jun Yang

PMC · DOI: 10.7717/peerj.20793 · PeerJ · 2026-02-16

## TL;DR

This study explores whether certain RNA and protein levels in early pregnancy can predict the risk of large babies in non-diabetic pregnancies.

## Contribution

The study is the first to investigate the association of lncRNA H19, miR-675, and PPARα with macrosomia in non-diabetic singleton pregnancies.

## Key findings

- Serum lncRNA H19 and miR-675 levels were not significantly associated with macrosomia risk.
- Lower PPARα protein levels were linked to reduced macrosomia risk in non-obese women.
- A combined model of the biomarkers showed better predictive performance than lipid-based models.

## Abstract

The roles of maternal serum lncRNA H19, miR-675, and  PPARα protein levels before mid-pregnancy in predicting macrosomia remain unclear. This study aimed to investigate whether the expression of these serum molecules is associated with the risk of macrosomia in singleton pregnancies without gestational diabetes mellitus.

A nested case-control study was conducted within a prospective cohort study of 898 women with singleton pregnancies. Mothers of liveborn macrosomic newborns constituted the case group, and a random sample of mothers of the normal-birthweight newborns, matched on gestational age at blood collection and delivery date, served as controls. Serum levels of lncRNA H19, miR-675,  PPARα protein, and serum lipids were measured before 20 weeks’ gestation. Logistic regression, restricted cubic spline analysis, and stratified analysis were used to assess the associations. Predictive performance was explored using area under the receiver operating characteristic curve, net reclassification index (NRI), and integrated discrimination improvement (IDI).

No significant differences were observed in lncRNA H19 (Z =  − 0.344, P = 0.731), miR-675 (Z =  − 1.376, P = 0.169), or  PPARα protein levels (Z < 0, P = 0.999) between macrosomia and control groups. However, in women with pre-pregnancy BMI < 24 kg/m2, lower  PPARα protein levels (tertile 2 vs. tertile 3) were associated with a 70% reduced risk of macrosomia (OR = 0.30, 95% CI [0.09–0.99],  P = 0.049). The NRI and IDI of the combined model incorporating serum lncRNA H19, miR-675, and PPARα protein levels were statistically superior to lipid-based models (P < 0.05).

Serum lncRNA H19 and miR-675 were not associated with macrosomia risk. Lower serum  PPARα protein levels in early pregnancy may be associated with a reduced risk of macrosomia, particularly in non-obese women. The combined biomarkers demonstrated preliminary predictive potential in exploratory analysis, but validation in larger cohorts is required.

## Linked entities

- **Genes:** H19 (H19 imprinted maternally expressed transcript) [NCBI Gene 283120], PPARA (peroxisome proliferator activated receptor alpha) [NCBI Gene 5465]
- **Proteins:** PPARA (peroxisome proliferator activated receptor alpha)
- **Diseases:** gestational diabetes mellitus (MONDO:0005406)

## Full-text entities

- **Genes:** IGF2 (insulin like growth factor 2) [NCBI Gene 3481] {aka C11orf43, GRDF, IGF-II, PP9974, SRS3}, PPARG (peroxisome proliferator activated receptor gamma) [NCBI Gene 5468] {aka CIMT1, FPLD3, GLM1, NR1C3, PPARG1, PPARG2}, Mir675 (microRNA 675) [NCBI Gene 100314133] {aka rno-mir-675}, H19 (H19 imprinted maternally expressed transcript) [NCBI Gene 309122] {aka ASM, ASM1, D11S813E}, PPARA (peroxisome proliferator activated receptor alpha) [NCBI Gene 5465] {aka NR1C1, PPAR, PPAR-alpha, PPARalpha, hPPAR}, H19 (H19 imprinted maternally expressed transcript) [NCBI Gene 283120] {aka ASM, ASM1, BWS, D11S813E, GMRSP, LINC00008}, MIR675 (microRNA 675) [NCBI Gene 100033819] {aka MIRN675, hsa-mir-675}, CAT (catalase) [NCBI Gene 847]
- **Diseases:** overweight (MESH:D050177), fetal overgrowth (MESH:D005315), GDM (MESH:D016640), adiposity (MESH:D018205), obese (MESH:D009765), weight gain (MESH:D015430), ovarian reserve (MESH:D010049), maternal (MESH:D000079262), congenital or genetic disorders (MESH:D030342), metabolic (MESH:D008659), congenital malformations (OMIM:163000), IDI (MESH:D010468), polycystic ovary syndrome (MESH:D011085), dyslipidemia (MESH:D050171), fetal growth restriction (MESH:D005317), reperfusion injury (MESH:D015427), diseases (MESH:D004194), birthweight (MESH:D001724), pre-eclampsia (MESH:D011225), myocardial ischemia (MESH:D017202), Macrosomia (MESH:D005320), infertility (MESH:D007246), metabolic, genetic, congenital, mental disorders (MESH:D001523)
- **Chemicals:** TRIzol (MESH:C411644), agarose (MESH:D012685), Lipid (MESH:D008055), SYBR Green (MESH:C098022), water (MESH:D014867), glucose (MESH:D005947), Formaldehyde (MESH:D005557), cholesterol (MESH:D002784), FBG (-), fatty acid (MESH:D005227), TG (MESH:D014280)
- **Species:** Homo sapiens (human, species) [taxon 9606], Rattus norvegicus (brown rat, species) [taxon 10116]
- **Cell lines:** HTR-8/SVneo — Homo sapiens (Human), Transformed cell line (CVCL_7162)

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12919319/full.md

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12919319/full.md

## References

35 references — full list in the complete paper: https://tomesphere.com/paper/PMC12919319/full.md

---
Source: https://tomesphere.com/paper/PMC12919319