Evidence map›Paper›PMID 42094141›Full record

ArticlemedRxiv : the preprint server for health sciences2026

Early-life dentine-based elemental biodynamics and cord blood telomere length.

Bhargavi Srinath, Rohitha Ravisekar, Kshitij Sachdev, Joseph Eggers, Libni Avib Torres Olascoaga, Nia McRae, Inessa Lopez, Chelsea A DeBolt, Aderonke Akinkugbe, Romana Ranchadiya and 12 more

Abstract readPreprint
In one paragraph

Article in medRxiv : the preprint server for health sciences, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

22 authors.

Bhargavi SrinathDepartment of Public Health, Icahn School of Medicine at Mount Sinai, New York, NY, United States.ORCID 0009-0000-5444-3307
Rohitha RavisekarDepartment of Public Health, Icahn School of Medicine at Mount Sinai, New York, NY, United States.ORCID 0009-0003-5506-5899
Kshitij SachdevDepartment of Epidemiology, University of Iowa College of Public Health, Iowa City, Iowa, United States.ORCID 0009-0008-5496-9032
Joseph EggersDepartment of Epidemiology, University of Iowa College of Public Health, Iowa City, Iowa, United States.
Libni Avib Torres OlascoagaCenter for Research on Nutrition and Health, National Institute of Public Health, Cuernavaca, Mexico.
Nia McRaeDepartment of Environmental Medicine, Icahn School of Medicine at Mount Sinai, New York, NY, United States.
Inessa LopezDepartment of Environmental Medicine, Icahn School of Medicine at Mount Sinai, New York, NY, United States.ORCID 0009-0009-0361-6816
Chelsea A DeBoltDepartment of Obstetrics, Gynecology and Reproductive Science, Icahn School of Medicine at Mount Sinai, New York, NY, United States.ORCID 0000-0002-9532-4109
Aderonke AkinkugbeDepartment of Environmental Medicine, Icahn School of Medicine at Mount Sinai, New York, NY, United States.ORCID 0000-0003-1207-9732
Romana RanchadiyaDepartment of Public Health, Icahn School of Medicine at Mount Sinai, New York, NY, United States.
Martha M Téllez-RojoCenter for Research on Nutrition and Health, National Institute of Public Health, Cuernavaca, Mexico.
Chris GenningsDepartment of Environmental Medicine, Icahn School of Medicine at Mount Sinai, New York, NY, United States.ORCID 0000-0002-6058-5907
Robert B WallaceDepartment of Epidemiology, University of Iowa College of Public Health, Iowa City, Iowa, United States.ORCID 0000-0003-2038-7145
Robert WrightDepartment of Environmental Medicine, Icahn School of Medicine at Mount Sinai, New York, NY, United States.ORCID 0000-0001-6079-2749
Rosalind J WrightDepartment of Public Health, Icahn School of Medicine at Mount Sinai, New York, NY, United States.ORCID 0000-0002-4262-2807
Manish AroraDepartment of Environmental Medicine, Icahn School of Medicine at Mount Sinai, New York, NY, United States.
Cecilia S AlcalaDepartment of Environmental Medicine, Icahn School of Medicine at Mount Sinai, New York, NY, United States.
Manasi AgrawalThe Dr. Henry D. Janowitz Division of Gastroenterology, Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, NY, United States.
Jamil M LaneDepartment of Environmental Medicine, Icahn School of Medicine at Mount Sinai, New York, NY, United States.
Maria J RosaDepartment of Environmental Medicine, Icahn School of Medicine at Mount Sinai, New York, NY, United States.
Shoshannah I EggersDepartment of Epidemiology, University of Iowa College of Public Health, Iowa City, Iowa, United States.ORCID 0000-0002-4321-9219
Vishal MidyaDepartment of Public Health, Icahn School of Medicine at Mount Sinai, New York, NY, United States.ORCID 0000-0002-6643-5176

Funding

Conduits: Mount Sinai Health System Translational Science HubUL1TR004419 · NCATS · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI Rosalind J Wright · 2022 to 2026
$46.4M
Untargeted Analysis ResourceU2CES026561 · NIEHS · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI WRIGHT, ROBERT O · 2015 to 2025
$24.5M
The Mount Sinai Transdisciplinary Center on Early Environmental ExposuresP30ES023515 · NIEHS · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI Robert O Wright · 2014 to 2026
$21.3M
Untargeted Analysis ResourceU2CES030859 · NIEHS · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI ARORA, MANISH · 2019 to 2025
$8.2M
Early Warning Systems for Childhood and Adult DisordersR35ES030435 · NIEHS · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI Manish Arora · 2020 to 2026
$6.7M
Organic-metal mixtures and neurodevelopmentR01ES026033 · NIEHS · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI Manish Arora, Robert O Wright · 2016 to 2026
$6.1M
Prenatal metal exposures and childhood telomere length attritionR21ES037112 · NIEHS · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI EGGERS, SHOSHANNAH IYLENE, MIDYA, VISHAL · 2025 to 2025
$445k
ATSDR CDC HHS R01 TS000324NCATS NIH HHS UL1 TR004419NIEHS NIH HHS P30 ES023515NIEHS NIH HHS R01 ES026033NIEHS NIH HHS R21 ES037112NIEHS NIH HHS R35 ES030435NIEHS NIH HHS U2C ES026561NIEHS NIH HHS U2C ES030859
6 · The paper itself

Abstract

Background: Leukocyte telomere length (LTL) from cord blood is a marker of biological aging and long-term systemic health. Exposure to essential and toxic metals has been shown to influence LTL in a sexually dimorphic manner. However, little is known about the interplay between early-life longitudinal biodynamic patterns of these elements and cord blood LTL, as well as potential sex differences. Methods: From an ongoing longitudinal birth cohort study in Mexico City, we used available tooth samples from 231 children (129 males and 102 females) to generate 16 elemental weekly time series of direct fetal intensities from the second trimester through four to five months after birth. We analyzed the dentine growth rings using Inductively Coupled Plasma Mass Spectrometry to generate time-resolved elemental intensities. The elements included were Li, Mg, Ca, Mn, Co, Ni, Cu, Zn, As, Sr, Mo, Cd, Sn, Ba, Pb, and Bi. LTL was measured in cord blood using qPCR. We used cross-recurrence quantification analysis and entropy-complexity-based measures to generate time-resolved features that quantify the synchronization of elemental biodynamics. A stability-selection approach using five-fold cross-validation of regularized ridge regression was used for feature selection, and covariate-adjusted linear models were used to estimate associations with LTL. Findings: The biodynamic interaction of Mg-Co and Mn-Sn was identified as the most stable feature among male and female children, respectively. In males, higher vertical entropy (i.e., a measure of higher variability) of Mg-Co temporal biodynamics was associated with shorter LTL (β[95%CI]: -0.9[-0.14,-0.03]; p-value<0.01), but not in females (β[95%CI]:-0.02[-0.10,0.06]; p-value=0.60); whereas higher recurrence rate (i.e., a measure of higher synchronicity) of Mn-Sn temporal biodynamics was associated with longer LTL (β[95%CI]: 0.09[0.02,0.16]; p-value=0.01), in females but not in males (β[95%CI], 0.03[-0.04, 0.09]; p-value=0.39). Interpretation: We demonstrate that time-varying multi-elemental synchronization of early-life elemental biodynamics, a potential marker of homeostatic balance, may be associated with cord blood-based telomere length in a sexual dimorphic manner.

Indexed as

Child HealthElemental BiodynamicsMachine LearningMetalsTelomere Aging

Identifiers

PMID42094141
PMCPMC13142602

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LicenceCC BY-NC-ND
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Registered trials

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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.