# Maternal Telomere Length and Its Influence on Neonatal Parameters: A Potential Tool for Prenatal Screening

**Authors:** Razvan Nitu, Tiberiu Dragomir, Simona-Alina Abu-Awwad, Flavius Olaru, Carmen-Ioana Marta, Ahmed Abu-Awwad, Bogdan Sorop, Mircea Diaconu

PMC · DOI: 10.3390/medicina61101755 · Medicina · 2025-09-26

## TL;DR

This study shows that longer telomeres in mothers are linked to better neonatal outcomes like higher birth weight and better Apgar scores.

## Contribution

The study provides novel evidence linking maternal telomere length to neonatal health in a Central/Eastern European population.

## Key findings

- Longer maternal telomere length correlates with higher birth weight, length, and head circumference.
- Maternal telomere length is strongly associated with higher Apgar scores at 1 and 5 minutes.
- Shorter maternal telomere length independently predicts suboptimal 1-minute Apgar scores.

## Abstract

Background and Objectives: Maternal telomere length (TL) has been proposed as a potential biomarker of biological aging and pregnancy outcomes, yet evidence in Central and Eastern European populations remains scarce. This study aimed to investigate the association between maternal TL and neonatal parameters in a clinically healthy cohort. Materials and Methods: We conducted a prospective observational study including 134 mother–infant pairs at the “Pius Brînzeu” Emergency County Clinical Hospital, Timișoara. All deliveries were performed by cesarean section for maternal indications unrelated to fetal condition. Maternal blood samples were collected at admission, and relative TL was measured by quantitative PCR. Neonatal outcomes included birth weight, length, head circumference, gestational age, and Apgar scores. Results: Longer maternal TL was positively correlated with birth weight (r = 0.515, p < 0.001), length (r = 0.559, p < 0.001), head circumference (r = 0.468, p < 0.001), gestational age (r = 0.444, p < 0.001), and Apgar scores at 1 (r = 0.714, p < 0.001) and 5 min (r = 0.684, p < 0.001). Logistic regression showed that shorter maternal TL independently predicted suboptimal 1 min Apgar (<8), with an adjusted odds ratio of 0.68 (95% CI: 0.51–0.91). Conclusions: Maternal TL is strongly associated with neonatal growth and vitality measures, supporting its potential as a simple, non-invasive biomarker for perinatal risk assessment.

## Full-text entities

- **Genes:** CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790] {aka CVID12, EBP-1, KBF1, NF-kB, NF-kB1, NF-kappa-B1}, HK1 (hexokinase 1) [NCBI Gene 3098] {aka CNSHA5, HK, HK1-ta, HK1-tb, HK1-tc, HKD}
- **Diseases:** aneuploidy (MESH:D000782), HIV/AIDS (MESH:D015658), preterm labor (MESH:D007752), thromboembolic (MESH:D013923), TL (MESH:C536801), prematurity (MESH:C536271), systemic (MESH:D015619), thyroid dysfunction (MESH:D013959), miscarriages (MESH:D000022), infection (MESH:D007239), preterm birth (MESH:D047928), endocrine/metabolic disorders (MESH:D004700), COVID-19 (MESH:D000086382), marrow dysfunction (MESH:D001855), nutritional deficiencies (MESH:D044342), micronutrient deficiency (MESH:D007153), hypertension (MESH:D006973), HCV (MESH:D006526), iron deficiency (MESH:D000090463), metabolic (MESH:D008659), structural anomaly (MESH:C536503), obesity (MESH:D009765), smoking (MESH:D015208), autoimmune diseases (MESH:D001327), HBV (MESH:D006509), drug or alcohol abuse (MESH:D019966), psychiatric (MESH:D001523), impaired glycemic (MESH:D060825), cancer (MESH:D009369), chromosomal or structural anomalies (MESH:D002869), diabetes (MESH:D003920), inflammation (MESH:D007249), disease (MESH:D004194), injury to (MESH:D014947), IUGR (MESH:D005317), fetal anomalies (MESH:D000013)
- **Chemicals:** glucose (MESH:D005947), reactive oxygen species (MESH:D017382), 25-hydroxyvitamin D (MESH:C104450), silica (MESH:D012822), TL (-), iron (MESH:D007501), EDTA (MESH:D004492), oxygen (MESH:D010100), Vitamin D (MESH:D014807)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## References

41 references — full list in the complete paper: https://tomesphere.com/paper/PMC12566357/full.md

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Source: https://tomesphere.com/paper/PMC12566357