Maternal smoking during pregnancy and newborn telomere length (TL): a systematic review and meta-analysis of observational studies
Open accessAbstract
BACKGROUND: Telomeres indicate cellular aging. Shortened telomeres are linked to various diseases and mortality, influenced by factors like inflammation, genetics, and environmental exposures, including smoking. Assessing newborn telomere length (TL) and maternal smoking association remains unexplored. A systematic review aims to fill this gap, potentially advancing clinical understanding and guiding future research. METHODS: This systematic review involved searching six English electronic databases—PubMed, Scopus, PsycINFO, Web of Science, Embase, and CINAHL Complete—for records from their inception until February 2024. The review focused solely on observational studies. Included studies assessed the impact of maternal smoking during pregnancy on the TL of newborns. The quality of these studies was evaluated using the Newcastle–Ottawa quality assessment scale. A random-effect model was employed, and the statistical analysis was conducted with Stata software version 17. RESULTS: Eight of 485 initial studies were included for systematic and five for meta-analysis. Eight studies involving 2,797 participants investigated prenatal smoking’s impact on infant telomere length, predominantly using qPCR and umbilical cord blood cells for measurement of TL. Five studies with 1,822 participants assessed the effect of maternal smoking during pregnancy on newborn TL, revealing a significant negative correlation (-0.19 [-0.32, -0.09]). Despite high heterogeneity (I2: 85.57%), no publication bias was found. Sensitivity analysis, excluding one study, showed a stronger correlation (-0.27 [-0.36, -0.17]) and reduced heterogeneity (I2: 53.21%). Subgroup analysis by nationality indicated a slightly stronger correlation in North American studies (-0.21 [-0.30, -0.12]) compared to Asian studies (-0.17 [-0.52, 0.17]). No significant differences were observed (p = 0.85). CONCLUSION: A meta-analysis found maternal smoking in pregnancy correlates negatively with neonatal telomere length, impacting aging. Urgent awareness and further research are needed for preventive measures.
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
Maternal stress, smoking, air pollution and heavy-metal exposure during pregnancy are associated with shorter or altered newborn telomere length, although effect direction and magnitude vary by exposure window, tissue and assay.
“Maternal stress, smoking, air pollution and heavy-metal exposure during pregnancy have been associated with shorter or altered newborn TL, although effect direction and magnitude vary by exposure window, tissue and assay [122,123,124,125,126].”
From Placental Pathophysiology and Developmental Programming of Adult Cardiometabolic Risk: A Narrative Review of Pregnancy Exposures (2026) · cites this paper as [125]
The Discussion reports that most studies found shorter newborn telomere length with maternal smoking, while some found longer telomeres or no association. It also mentions maternal stress and air pollution as influences on early-life telomere length, but does not establish the claimed prenatal associations for air pollution or heavy-metal exposure. The passages do not substantiate tissue and assay as reasons for the variation across all four exposures. (LLM, conf=0.87)
Experimental — accuracy not yet measuredPooled evidence supports shorter newborn telomere length after maternal smoking and an overall inverse association with prenatal metal exposure, with more consistent findings for cadmium and later-pregnancy exposure.
“Pooled evidence supports shorter newborn TL after maternal smoking and an overall inverse association with prenatal metal exposure, with more consistent findings for cadmium and later-pregnancy exposure [124,125].”
From Placental Pathophysiology and Developmental Programming of Adult Cardiometabolic Risk: A Narrative Review of Pregnancy Exposures (2026) · cites this paper as [125]
These associations show that prenatal exposures can coincide with early differences in telomere biology; they do not establish that neonatal telomere length mediates adult disease.
“These associations show that prenatal exposures can coincide with early differences in telomere biology; they do not establish that neonatal TL mediates adult disease.”
From Placental Pathophysiology and Developmental Programming of Adult Cardiometabolic Risk: A Narrative Review of Pregnancy Exposures (2026) · cites this paper as [125]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
The citation lists haven’t been fetched yet
References 46 · Cited by 2
Research works printed but not linked: 43
- [1]McClintock B. The stability of broken ends of chromosomes in Zea mays. Genetics. 1941;26(2):234–82. 17247004 PMC1209127 · DOI
- [2]Boukamp P, Mirancea N. Telomeres rather than telomerase a key target for anti-cancer therapy? Exp Dermatol. 2007;16(1):71–9. 17181645 · DOI
- [3]Blackburn EH. Structure and function of telomeres. Nature. 1991;350(6319):569–73. 1708110 · DOI · Paper page
- [4]Zakian VA. Structure, function, and replication of Saccharomyces cerevisiae telomeres. Annu Rev Genet. 1996;30:141–72. 8982452 · DOI
- [5]Rizvi S, Raza ST, Mahdi F. Telomere length variations in aging and age-related diseases. Curr Aging Sci. 2014;7(3):161–7. 25612739 · DOI
- [6]Wang Q, Zhan Y, Pedersen NL, Fang F, Hägg S. Telomere length and all-cause mortality: a meta-analysis. Ageing Res Rev. 2018;48:11–20. 30254001 · DOI
- [7]Wentzensen IM, Mirabello L, Pfeiffer RM, Savage SA. The association of telomere length and cancer: a meta-analysis. Cancer Epidemiol Biomarkers Prev. 2011;20(6):1238–50. 21467229 PMC3111877 · DOI · Paper page
- [8]Zhao J, Miao K, Wang H, Ding H, Wang DW. Association between telomere length and type 2 diabetes mellitus: a meta-analysis. PLoS ONE. 2013;8(11):e79993. 24278229 PMC3836967 · DOI
- [10]Birch J, Barnes PJ, Passos JF. Mitochondria, telomeres and cell senescence: implications for lung ageing and disease. Pharmacol Ther. 2018;183:34–49. 28987319 · DOI
- [11]Masi S, Nightingale CM, Day IN, Guthrie P, Rumley A, Lowe GD, et al. Inflammation and not cardiovascular risk factors is associated with short leukocyte telomere length in 13- to 16-year-old adolescents. Arterioscler Thromb Vasc Biol. 2012;32(8):2029–34. 22679311 · DOI
- [12]Needham BL, Mezuk B, Bareis N, Lin J, Blackburn EH, Epel ES. Depression, anxiety and telomere length in young adults: evidence from the National health and nutrition examination survey. Mol Psychiatry. 2015;20(4):520–8. 25178165 PMC4346549 · DOI
- [13]Cawthon RM, Smith KR, O’Brien E, Sivatchenko A, Kerber RA. Association between telomere length in blood and mortality in people aged 60 years or older. Lancet. 2003;361(9355):393–5. 12573379 · DOI · Paper page
- [14]Njajou OT, Cawthon RM, Damcott CM, Wu SH, Ott S, Garant MJ, et al. Telomere length is paternally inherited and is associated with parental lifespan. Proc Natl Acad Sci U S A. 2007;104(29):12135–9. 17623782 PMC1924539 · DOI · Paper page
- [17]Nawrot TS, Staessen JA, Gardner JP, Aviv A. Telomere length and possible link to X chromosome. Lancet. 2004;363(9408):507–10. 14975611 · DOI
- [19]Moshfeghinia R, Torabi A, Mostafavi S, Rahbar S, Moradi MS, Sadeghi E, et al. Maternal psychological stress during pregnancy and newborn telomere length: a systematic review and meta-analysis. BMC Psychiatry. 2023;23(1):947. 38102621 PMC10724935 · DOI
- [20]von Zglinicki T. Oxidative stress shortens telomeres. Trends Biochem Sci. 2002;27(7):339–44. 12114022 · DOI · Paper page
- [21]Freitas-Simoes TM, Ros E, Sala-Vila A. Nutrients, foods, dietary patterns and telomere length: update of epidemiological studies and randomized trials. Metabolism. 2016;65(4):406–15. 26975532 · DOI
- [22]Pieters N, Janssen BG, Dewitte H, Cox B, Cuypers A, Lefebvre W, et al. Biomolecular markers within the core axis of aging and particulate air pollution exposure in the elderly: a cross-sectional study. Environ Health Perspect. 2016;124(7):943–50. 26672058 PMC4937852 · DOI
- [23]Latifovic L, Peacock SD, Massey TE, King WD. The influence of alcohol consumption, cigarette smoking, and physical activity on leukocyte telomere length. Cancer Epidemiol Biomarkers Prev. 2016;25(2):374–80. 26656293 · DOI
- [25]Liu B, Song L, Zhang L, Wu M, Wang L, Cao Z, et al. Prenatal second-hand smoke exposure and newborn telomere length. Pediatr Res. 2020;87(6):1081–5. 31578036 · DOI
- [26]Factor-Litvak P, Susser E, Kezios K, McKeague I, Kark JD, Hoffman M, et al. Leukocyte telomere length in newborns: implications for the role of telomeres in human disease. Pediatrics. 2016. 10.1542/peds.2015-3927. 26969272 PMC4811318 · DOI
- [27]Chow CK. Cigarette smoking and oxidative damage in the lung. Ann N Y Acad Sci. 1993;686:289–98. 8512254 · DOI
- [28]Thorne D, Wilson J, Kumaravel TS, Massey ED, McEwan M. Measurement of oxidative DNA damage induced by mainstream cigarette smoke in cultured NCI-H292 human pulmonary carcinoma cells. Mutat Res. 2009;673(1):3–8. 19100859 · DOI
- [29]Yanbaeva DG, Dentener MA, Creutzberg EC, Wesseling G, Wouters EF. Systemic effects of smoking. Chest. 2007;131(5):1557–66. 17494805 · DOI
- [30]Wei H, Zhang C, Silveyra P. The relationships between prenatal smoking exposure and telomere lengths in fetuses, infants, and children: a systematic literature review. J Addict Nurs. 2020;31(4):243–52. 33264196 · DOI
- [33]Almanzar G, Eberle G, Lassacher A, Specht C, Koppelstaetter C, Heinz-Erian P, et al. Maternal cigarette smoking and its effect on neonatal lymphocyte subpopulations and replication. BMC Pediatr. 2013;13:1–8. 23597118 PMC3644263 · DOI · Paper page
- [34]Bosquet Enlow M, Petty CR, Hacker MR, Burris HH. Maternal psychosocial functioning, obstetric health history, and newborn telomere length. Psychoneuroendocrinology. 2021;123:105043. 33176222 PMC7732207 · DOI
- [35]Chen L, Tan KML, Gong M, Chong MF, Tan KH, Chong YS, et al. Variability in newborn telomere length is explained by inheritance and intrauterine environment. BMC Med. 2022;20(1):20. 35073935 PMC8787951 · DOI
- [36]Enlow MB, Bollati V, Sideridis G, Flom JD, Hoxha M, Hacker MR, Wright RJ. Sex differences in effects of maternal risk and protective factors in childhood and pregnancy on newborn telomere length. Psychoneuroendocrinology. 2018;95:74–85. 29803183 PMC6109592 · DOI
- [37]Hahn MC, Werlang ICR, Rechenmacher C, Morais RVd, Barbé-Tuana FM, Grun LK, et al. Telomere length in healthy newborns is not affected by adverse intrauterine environments. Genet Mol Biol. 2021;44:e20200411. 34874050 PMC8647199 · DOI
- [38]Imam T, Jitratkosol MH, Soudeyns H, Sattha B, Gadawski I, Maan E, et al. Leukocyte telomere length in HIV-infected pregnant women treated with antiretroviral drugs during pregnancy and their uninfected infants. JAIDS J Acquir Immune Defic Syndr. 2012;60(5):495–502. 22580562 · DOI
- [39]Minamoto T, Nakayama K, Ishibashi T, Ishikawa M, Nakamura K, Yamashita H, et al. Pregnancy by assisted reproductive technology is associated with shorter telomere length in neonates. Int J Mol Sci. 2020;21(24):9688. 33353140 PMC7766074 · DOI
- [40]Salihu HM, Pradhan A, King L, Paothong A, Nwoga C, Marty PJ, Whiteman V. Impact of intrauterine tobacco exposure on fetal telomere length. Am J Obstet Gynecol. 2015;212(2):205. e1-. e8. 25173189 · DOI
- [41]Babizhayev MA, Yegorov YE. Smoking and health: association between telomere length and factors impacting on human disease, quality of life and life span in a large population-based cohort under the effect of smoking duration. Fundam Clin Pharmacol. 2011;25(4):425–42. 20698892 · DOI
- [42]Babizhayev MA, Savel’yeva EL, Moskvina SN, Yegorov YE. Telomere length is a biomarker of cumulative oxidative stress, biologic age, and an independent predictor of survival and therapeutic treatment requirement associated with smoking behavior. Am J Ther. 2011;18(6):e209–26. 20228673 · DOI
- [43]Córdova-Oriz I, Chico-Sordo L, Varela E. Telomeres, aging and reproduction. Curr Opin Obstet Gynecol. 2022;34(3):151–8. 35645014 · DOI
- [44]Gorenjak V, Petrelis AM, Stathopoulou MG, Visvikis-Siest S. Telomere length determinants in childhood. Clin Chem Lab Med. 2020;58(2):162–77. 31465289 · DOI
- [45]Whiteman VE, Goswami A, Salihu HM. Telomere length and fetal programming: a review of recent scientific advances. Am J Reprod Immunol. 2017. 10.1111/aji.12661. 28500672 · DOI
- [46]Werlang ICR, Hahn MC, Bernardi JR, Nast M, Goldani MZ, Michalowski MB. Exposure to different intrauterine environments: implications for telomere attrition in early life. J Matern Fetal Neonatal Med. 2019;32(21):3675–84. 29681194 · DOI
- [47]Bateson M, Aviv A, Bendix L, Benetos A, Ben-Shlomo Y, Bojesen SE, et al. Smoking does not accelerate leucocyte telomere attrition: a meta-analysis of 18 longitudinal cohorts. R Soc Open Sci. 2019;6(6):190420. 31312500 PMC6599800 · DOI
- [48]Eisenberg DT. An evolutionary review of human telomere biology: the thrifty telomere hypothesis and notes on potential adaptive paternal effects. Am J Hum Biol. 2011;23(2):149–67. 21319244 · DOI
- [49]Almanzar G, Eberle G, Lassacher A, Specht C, Koppelstaetter C, Heinz-Erian P, et al. Maternal cigarette smoking and its effect on neonatal lymphocyte subpopulations and replication. BMC Pediatr. 2013;13:57. 23597118 PMC3644263 · DOI · Paper page
- [50]Delcroix-Gomez C, Delcroix MH, Jamee A, Gauthier T, Marquet P, Aubard Y. Fetal growth restriction, low birth weight, and preterm birth: effects of active or passive smoking evaluated by maternal expired CO at delivery, impacts of cessation at different trimesters. Tob Induc Dis. 2022;20:70. 36118558 PMC9413415 · DOI
- Authors
- Moshfeghinia, R., Ghahremani, M., Ghasemi, A. R., Mostafavi, S., Mohagheghzadeh, H., Maharlouei, N., Ahmadi, J., & Vardanjani, H. M.
- Affiliations
- Shiraz University of Medical Sciences (IR)
- Arak University of Medical Sciences (IR)
- Ankara Medipol Üniversitesi (TR)
- Corresponding author
- Moshfeghinia, Reza
- Vardanjani, Hossein Molavi
- Venue
- BMC Pregnancy and Childbirth
- Published
- 2025-12-16
- Volume
- 26
- Issue
- 1
- Pages
- 67-67
- ISSN
- 1471-2393 (ISSN-L)
- PMC
- PMC12822185
- OpenAlex
- W4417414324
- Cited by
- 2
- References
- 46
- Citations by year
- 2026: 2
- FWCI
- 0.26
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- BMC Pregnancy and Childbirth (publishedVersion, cc-by-nc-nd)
- PubMed (publishedVersion)
- PubMed Central (publishedVersion, cc-by-nc-nd)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Topics
- Health Sciences › Medicine › Physiology › Telomeres, Telomerase, and Senescence
- Health Sciences › Medicine › Physiology › Smoking Behavior and Cessation
- Health Sciences › Medicine › Pediatrics, Perinatology and Child Health › Prenatal Substance Exposure Effects
- Keywords
- smoking during pregnancy, prenatal tobacco exposure, cellular aging, umbilical cord blood, maternal smoking
- MeSH terms
- Female, Humans, Infant, Newborn, Pregnancy, Prenatal Exposure Delayed Effects, Smoking, Telomere, Telomere Shortening, Observational Studies as Topic
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review