Organ-Specific Toxic Effects and Biomarker Evidence of Pyrethroid in Vulnerable Populations: A Systematic Review
Abstract
Pyrethroid exposure through ingestion, inhalation, or dermal contact may trigger toxic effects in the human body, with severity potentially increasing in certain vulnerable populations. We aim to summarize the evidence regarding pyrethroid exposure and organ-specific toxic effects in children, pregnant and breastfeeding women, and the elderly. Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines were used in this study. The search strategy was designed considering the population, exposure, controls, and outcomes (PECO). The scientific databases PubMed, Scopus, Google Scholar, and Science Direct were systematically searched for relevant literature published from 1990 to April 2025. Observational studies which meeting the inclusion criteria of were included. Two authors independently searched the database, assessed the risks of bias and extracted the data from the shortlisted articles. Out of the 7259 records collated, 25 studies were included in this review, there are 13 crossectional studies and 12 cohort studies. The studies investigated the related to the nervous system (n= 14), the endocrine system (n= 5), the lungs (n= 3), the reproductive organs (n= 2), and the auditory system (n= 1). The quality of the studies varied with overall grades derived from the bias analysis ranging from low to moderate bias. Selected articles revealed that the reproductive organs, lungs, ears, as well as the nervous and endocrine systems are particularly vulnerable to pyrethroid toxicity. All studies suggest a possible role for pyrethoid exposure and organ-specific toxic effects characterized by alterations in biochemical markers and organ function. Although further research is still needed, existing studies suggest that 3-phenoxybenzoic acid (3-PBA) is commonly used as a urinary biomarker of pyrethroid exposure.
Keywords: pyrethroid, children, pregnant and breastfeeding women, pyrethroid
References
Hodoșan C, Gîrd CE, Ghica MV, Dinu-Pîrvu CE, Nistor L, Bărbuică IS, et al. Pyrethrins and pyrethroids: a comprehensive review of natural occurring compounds and their synthetic derivatives. Plants. 2023;12(23):4022, CrossRef.
Ahamad A, Kumar J. Pyrethroid pesticides: An overview on classification, toxicological assessment and monitoring. J Hazard Mater Adv. 2023;10:100284, CrossRef.
Lee KS, Lim YH, Lee YA, Shin CH, Kim BN, Hong YC, et al. The association of prenatal and childhood pyrethroid pesticide exposure with school-age ADHD traits. Environ Int. 2022;161:107124, CrossRef.
Singh S, Mukherjee A, Jaiswal DK, De Araujo Pereira AP, Prasad R, Sharma M, et al. Advances and future prospects of pyrethroids: Toxicity and microbial degradation. Sci Total Environ. 2022;829:154561, CrossRef.
Ye X, Pan W, Zhao Y, Zhao S, Zhu Y, Liu W, et al. Association of pyrethroids exposure with onset of puberty in Chinese girls. Environ Pollut. 2017;227:606-12, CrossRef.
Poole ND, Schaffer DH. Pyrethrin and pyrethroid toxicity. In: StatPearls. Treasure Island (FL): StatPearls Publishing; 2025, Article.
Roberts JR, Karr CJ. Pesticide exposure in children. Pediatrics. 2012;130(6):1765-88, CrossRef.
Yanagihara T, Nakagawa T, Fukushima T, Moriuchi Y, Ogata H, Ishimatsu A, et al. Acute pneumonitis associated with the inhalation of pyrethroid-based domestic insecticides. Cureus. 15(8):e43200, CrossRef.
Bornman R, Acerini CL, Chevrier J, Rauch S, Crause M, Obida M, et al. Maternal exposure to DDT, DDE, and pyrethroid insecticides for malaria vector control and hypospadias in the VHEMBE birth cohort study, Limpopo, South Africa. Science of The Total Environment. 2022;845:157084, CrossRef.
Mueller W, Atuhaire A, Mubeezi R, Van Den Brenk I, Kromhout H, Basinas I, et al. Evaluation of two-year recall of self-reported pesticide exposure among Ugandan smallholder farmers. Int J Hygand Environ Health. 2022;240:113911, CrossRef.
Ye X, Pan W, Zhao S, Zhao Y, Zhu Y, Liu J, et al. Relationships of pyrethroid exposure with gonadotropin levels and pubertal development in chinese boys. Environ Sci Technol. 2017;51: 6379-86, CrossRef.
Kunno J, Ong-Artborirak P, Taneepanichskul N, Robson MG, Siriwong W. Effect of pyrethroid insecticides exposure in relation to pyrethroid metabolite and GABA concentration of young children, Bangkok Thailand. Hum Ecol Risk Assess: Int J. 2021;27; 1-14, CrossRef.
Bornman R, Acerini CL, Chevrier J, Rauch S, Crause M, Obida M, et al. Maternal exposure to DDT, DDE, and pyrethroid insecticides for malaria vector control and hypospadias in the VHEMBE birth cohort study, Limpopo, South Africa. Sci Total Environ. 2022;845:157084, CrossRef.
Corrales Vargas A, Peñaloza Castañeda J, Rietz Liljedahl E, Mora AM, Menezes-Filho JA, Smith DR, et al. Exposure to common-use pesticides, manganese, lead, and thyroid function among pregnant women from the Infants' Environmental Health (ISA) study, Costa Rica. Sci Total Environ. 2022;810:151288, CrossRef.
Hu P, Su W, Vinturache A, Gu H, Cai C, Lu M, et al. Urinary 3-phenoxybenzoic acid (3-PBA) concentration and pulmonary function in children: A national health and nutrition examination survey (NHANES) 2007-2012 analysis. Environ Pollut. 2021;270:116178, CrossRef.
Ye M, Beach J, Martin JW, Senthilselvan A. Urinary concentrations of pyrethroid metabolites and its association with lung function in a Canadian general population. Occup Environ Med. 2016;73(2):119-26, CrossRef.
Kim JH, Lee S, Kim KN, Hong YC. Association of urinary 3-phenoxybenzoic acid level with pulmonary function reduction in an urban elderly population with repeated measures data. Environ Pollut. 2019;246:811-8, CrossRef.
Xu H, Mao Y, Xu B. Association between pyrethroid pesticide exposure and hearing loss in adolescents. Environ Res. 2020;187:109640, CrossRef.
Normann SS, Ma Y, Andersen HR, Valente MJ, Renko K, Arnold S, et al. Pyrethroid exposure biomarker 3-phenoxybenzoic acid (3-PBA) binds to transthyretin and is positively associated with free T3 in pregnant women. International Journal of Hygiene and Environ Health. 2025;264:114495, CrossRef.
Chevrier J, Rauch S, Obida M, Crause M, Bornman R, Eskenazi B. Sex and poverty modify associations between maternal peripartum concentrations of DDT/E and pyrethroid metabolites and thyroid hormone levels in neonates participating in the VHEMBE study, South Africa. Environ Int. 2019;131:104958, CrossRef.
Freire C, Suárez B, Vela-Soria F, Castiello F, Reina-Pérez I, Andersen HR, et al. Urinary metabolites of non-persistent pesticides and serum hormones in Spanish adolescent males. Environ Res. 2021;197:111016, CrossRef.
Li J, Song X, Luo T, Loo KK, Chen S, Gui T. Effects of daily exposure to pyrethroid pesticides during infancy on children neurodevelopment at age four: A prospective study in rural Yunnan, China. Neurotoxicology. 2025;108:105-12, CrossRef.
Ntantu Nkinsa P, Fisher M, Muckle G, Guay M, Arbuckle TE, Fraser W, et al. Childhood exposure to pyrethroids and neurodevelopment in Canadian preschoolers. Neurotoxicology. 2023;99:120-8, CrossRef.
van Wendel de Joode B, Mora AM, Lindh CH, Hernández-Bonilla D, Córdoba L, Wesseling C, et al. Pesticide exposure and neurodevelopment in children aged 6-9 years from Talamanca, Costa Rica. Cortex. 2016;85:137-50, CrossRef.
Wang A, Wan Y, Mahai G, Qian X, Li Y, Xu S, et al. Association of prenatal exposure to organophosphate, pyrethroid, and neonicotinoid insecticides with child neurodevelopment at 2 years of age: A prospective cohort study. Environ Health Perspect. 2023;131:107011, CrossRef.
Rodriguez PM, Ondarza PM, Miglioranza KSB, Ramirez CL, Vera B, Muntaner C, et al. Pesticides exposure in pregnant Argentinian women: Potential relations with the residence areas and the anthropometric neonate parameters. Chemosphere. 2023;332:138790, CrossRef.
Kim UJ, Hong M, Choi YH. Environmental pyrethroid exposure and cognitive dysfunction in U.S. Older adults: the NHANES 2001-2002. Int J Environ Res Public Health. 2021;18(22):12005, CrossRef.
Eskenazi B, An S, Rauch SA, Coker ES, Maphula A, Obida M, et al. Prenatal Exposure to DDT and Pyrethroids for Malaria Control and Child Neurodevelopment: The VHEMBE Cohort, South Africa. Environ Health Perspect. 2018;126:047004-1, CrossRef.
Wang N, Huang M, Guo X, Lin P. Urinary metabolites of organophosphate and pyrethroid pesticides and neurobehavioral effects in chinese children. Environ Sci Technol. 2016;50:9627, CrossRef.
Viel JF, Warembourg C, Le Maner-Idrissi G, Lacroix A, Limon G, Rouget F, et al. Pyrethroid insecticide exposure and cognitive developmental disabilities in children: The PELAGIE mother-child cohort. Environ Int. 2015;82:69-75, CrossRef.
Yen J, Yang K, Tu XM, Kayser G, Skomal A, Gahagan S, et al. Associations between neonicotinoid, pyrethroid, and organophosphate insecticide metabolites and neurobehavioral performance in ecuadorian adolescents. Medrxiv. 2024; 11:2024.10.10.24315201, CrossRef.
Qi Z, Song X, Xiao X, Loo KK, Wang MC, Xu Q, et al. Effects of prenatal exposure to pyrethroid pesticides on neurodevelopment of 1-year- old children: A birth cohort study in China. Ecotoxicology and Environmental Safety. 2022;234:113384, CrossRef.
Fluegge KR, Nishioka M, Wilkins JR. Effects of simultaneous prenatal exposures to organophosphate and synthetic pyrethroid insecticides on infant neurodevelopment at three months of age. J Environ Toxicol Public Health. 2016;1:60-73, Article.
Chen S, Xiao X,Qi Z, Chen L, Chen Y, Xu L, et al. Effects of prenatal and infant daily exposure to pyrethroid pesticides on the language development of 2-year-old toddlers: A prospective cohort study in rural Yunnan, China. Neurotoxicology. 2022;92:180-90, CrossRef.
Corcellas C, Eljarrat E, Barceló D. Enantiomeric-selective determination of pyrethroids: application to human samples. Anal Bioanal Chem. 2015;407(3):779-86, CrossRef.
Patel M, Patil P. Synthetic Pyrethroids: Toxicity and Metabolism. IOSR J Environ Sci Toxicol Food Technol. 2016;09(10):55-60, CrossRef.
Hołyńska-Iwan I, Szewczyk-Golec K. Pyrethroids: how they affect human and animal health?. Medicina. 2020;56:582, CrossRef.
Bhatt P, Huang Y, Zhan H, Chen S. Insight into microbial applications for the biodegradation of pyrethroid insecticides. Front Microbiol. 2019;10:1778, CrossRef.
Mikata K, Isobe N, Kaneko H. Biotransformation and enzymatic reactions of synthetic pyrethroids in mammals. Top Curr Chem. 2012;314:113-35, CrossRef.
Scollon EJ, Starr JM, Godin SJ, DeVito MJ, Hughes MF. In vitro metabolism of pyrethroid pesticides by rat and human hepatic microsomes and cytochrome p450 isoforms. Drug Metab Dispos. 2009;37(1):221-8, CrossRef.
Kaneko H. Biotransformation and enzymes responsible for metabolism of pyrethroids in mammals. In: Krishnan K, editor. Parameters for pesticide QSAR and PBPK/PD models for human risk assessment. Washington (DC): American Chemical Society; 2012:41-52, CrossRef.
Barr DB, Olsson AO, Wong LY, Udunka S, Baker SE, Whitehead Jr. RD, et al. Urinary concentrations of metabolites of pyrethroid insecticides in the general U.S. population: national health and nutrition examination survey 1999-2002. Environ Health Perspect. 2010;118(6):742-8, CrossRef.
Lehmler HJ, Simonsen D, Liu B, Bao W. Environmental exposure to pyrethroid pesticides in a nationally representative sample of U.S. adults and children: the national health and nutrition examination survey 2007-2012. Environ Pollut. 2020;267:115489, CrossRef.
Cycoń M, Piotrowska-Seget Z. Pyrethroid-degrading microorganisms and their potential for the bioremediation of contaminated soils: a review. Front microbiol. 2016;15;7:1463, CrossRef.
Chen H, Wang X, Liu P, Jia Q, Han H, Jiang C. Determination of three typical metabolites of pyrethroid pesticides in tea using a modified quechers sample preparation by ultra-high performance liquid chromatography tandem mass spectrometry. Foods. 2021;10(1):189, CrossRef.
de Lima Feltraco, Lizot L, Bastiani MF, Hahn RZ, Meireles YF, Freitas M, et al. Determination of the pyrethroid inseticide metabolite 3-phenoxybenzoic acid in wastewater using polar organic integrative samplers and LC-MS/MS analysis. Microchem J. 2023;190:108574, CrossRef.
Quindroit P, Crépet A, Brochot C. Estimating human exposure to pyrethroids' mixtures from biomonitoring data using physiologically based pharmacokinetic modeling. Environ Res. 2021;192:110281, CrossRef.
Ye X, Liu J. Effects of pyrethroid insecticides on hypothalamic-pituitary-gonadal axis: A reproductive health perspective. Environmental Pollution. 2019;245:590-9, CrossRef.
Di Stadio A, Frohman EM, Messineo D, Brenner MJ, Bernitsas E. The bidirectional brain-cochlea axis: a scaffold for neurologic disease-associated hearing loss. Brain Commun. 2024;6(6):fcae403, CrossRef.
Kulcsarova K, Bang C, Berg D, Schaeffer E. Pesticides and the microbiome-gut-brain axis: convergent pathways in the pathogenesis of parkinson's disease. J Parkinsons Dis. 2023;13(7):1079-106, CrossRef.
Rudmann DG. On-target and off-target-based toxicologic effects. Toxicol Pathol. 2013 ;41(2):310-4, CrossRef.
Field LM, Emyr Davies TG, O'Reilly AO, Williamson MS, Wallace BA. Voltage-gated sodium channels as targets for pyrethroid insecticides. Eur Biophys J. 2017;46(7):675-9, CrossRef.
Soderlund DM. Molecular mechanisms of pyrethroid insecticide neurotoxicity: recent advances. Arch Toxicol. 2012;86(2):165-81, CrossRef.
Shringi KL, Dulara SC, Aseri RK, Daria U. Uncontrolled seizures and unusual rise in leucocyte counts: transfluthrin, liquid mosquito repellent suicidal poisoning. Indian J Anaesth. 2015;59(1):47, CrossRef.
Ahamad A, Kumar J. Pyrethroid pesticides: An overview on classification, toxicological assessment and monitoring. Journal of Hazardous Materials Advances. 2023;10:100284, CrossRef.
Williams MT, Gutierrez A, Vorhees CV. Effects of acute deltamethrin exposure in adult and developing sprague dawley rats on acoustic startle response in relation to deltamethrin brain and plasma concentrations. Toxicol Sci. 2019;168(1):61-9, CrossRef.
Ileriturk M, Kandemir O, Kandemir FM. Evaluation of protective effects of quercetin against cypermethrin induced lung toxicity in rats via oxidative stress, inflammation, apoptosis, autophagy, and endoplasmic reticulum stress pathway. Environmental Toxicology. 2022;37(11):2639-50, CrossRef.
Hussien HM, Abdou HM, Yousef MI. Cypermethrin induced damage in genomic DNA and histopathological changes in brain and haematotoxicity in rats: The protective effect of sesame oil. Brain Research Bulletin. 2013;92:76-83, CrossRef.
Sharma P, Singh R, Jan M. Dose-dependent effect of deltamethrin in testis, liver, and kidney of wistar rats. Toxicol Int. 2014;21(2):131-9, CrossRef.
Tennekes HA, Sánchez-Bayo F. The molecular basis of simple relationships between exposure concentration and toxic effects with time. Toxicology. 2013;309:39-51, CrossRef.
Park YC, Lee S, Cho MH. The simplest flowchart stating the mechanisms for organic xenobiotics-induced toxicity: can it possibly be accepted as a "central dogma" for toxic mechanisms?. Toxicol Res. 2014;30(3):179-84, CrossRef.
Ramchandra AM, Chacko B, Victor PJ. Pyrethroid Poisoning. Indian J Crit Care Med. 2019;23(Suppl 4):S267-71, CrossRef.
Clark JM, Symington SB. Neurotoxic implications of the Agonistic action of CS-syndrome pyrethroids on the N-type Ca v 2.2 calcium channel. Pest Management Sci. 2008;64:628-38, CrossRef.
Vester AI, Chen M, Marsit CJ, Caudle WM. A neurodevelopmental model of combined pyrethroid and chronic stress exposure. Toxics. 2019;7(2):24, CrossRef.
Von Ehrenstein OS, Ling C, Cui X, Cockburn M, Park AS, Yu F, et al. Prenatal and infant exposure to ambient pesticides and autism spectrum disorder in children: population based case-control study. BMJ. 2019;364:l962, CrossRef.
Hu Y, Zhang Z, Qin K, Zhang Y, Pan R, Wang Y, et al. Environmental pyrethroid exposure and thyroid hormones of pregnant women in Shandong, China. Chemosphere. 2019;234:815-21, CrossRef.
Xu L, Yang S, Wang L, Qiu J, Meng H, Zhang L, et al. Association between pesticide exposure and thyroid function: analysis of Chinese and NHANES databases. Front Public Health. 2024;12, CrossRef.
Sirikul W, Sapbamrer R. Exposure to pesticides and the risk of hypothyroidism: a systematic review and meta-analysis. BMC Public Health. 2023;23(1):1867, CrossRef.
Sakali AK, Bargiota A, Fatouros IG, Jamurtas A, Macut D, Mastorakos G, et al. Effects on puberty of nutrition-mediated endocrine disruptors employed in agriculture. Nutrients. 2021;13(11):4184, CrossRef.
Ye X, Li F, Zhang J, Ma H, Ji D, Huang X, et al. Pyrethroid insecticide cypermethrin accelerates pubertal onset in male mice via disrupting hypothalamic-pituitary-gonadal axis. Environ Sci Technol. 2017;51(17):10212-21, CrossRef.
Lan H, Hu Z, Gan H, Wu L, Xie S, Jiang Y, et al. Association between exposure to persistent organic pollutants and pubertal timing in boys and girls: A systematic review and meta-analysis. Ecotoxicol Environ Saf. 2023;265:115540, CrossRef.
Vorselaars ADM, Van Den Berg PM, Drent M. Severe pulmonary toxicity associated with inhalation of pyrethroid-based domestic insecticides (Bop/Sapolio): a case series and literature review. Curr Opin Pulm Med. 2021;27(4):271-7, CrossRef.
Pauluhn J. Upper respiratory tract nociceptor stimulation and stress response following acute and repeated Cyfluthrin inhalation in normal and pregnant rats: Physiological rat-specific adaptions can easily be misunderstood as adversities. Toxicol Lett. 2018;282:8-24, CrossRef.
Yanagihara T, Nakagawa T, Fukushima T, Moriuchi Y, Ogata H, Ishimatsu A. Acute pneumonitis associated with the inhalation of pyrethroid-based domestic insecticides. Cureus. 2023;15(8):e43200, CrossRef.
Cunha EO, Reis AD, Macedo MB, Machado MS, Dallegrave E. Ototoxicity of cypermethrin in Wistar rats. Braz J Otorhinolaryngol. 2020;86(5):587-92, CrossRef.
Gatto MP, Fioretti M, Fabrizi G, Gherardi M, Strafella E, Santarelli L. Effects of potential neurotoxic pesticides on hearing loss: A review. Neurotoxicology. 2014;42:24-32, CrossRef.
Saha R, Dutta SM. Pyrethroids have become a barrier to the daily existence of molluscs (review). J Hazard Mater Lett. 2025;6:100144, CrossRef.
Kunno J, Ong-Artborirak P, Panicharoen P, Robson MG, Siriwong W. Pyrethroid insecticides in households from urban areas: an association of the 3-pba metabolite and hand wipes. Ann Glob Health. 2020;86(1):1-7, CrossRef.
Corcellas C, Feo ML, Torres JP, Malm O, Ocampo-Duque W, Eljarrat E, et al. Pyrethroids in human breast milk: Occurrence and nursing daily intake estimation. Environment International. 2012;47:17-22, CrossRef.
Preston J, Biddell B. The physiology of ageing and how these changes affect older people. Medicine. 2021;49(1):1-5, CrossRef.
Scheepers LD, Freercks R, Merwe E van der. Acute cypermethrin and other pyrethroid poisoning - An organophosphate-like poisoning: A case report and review. Toxicol Rep. 2023;11:107-10, CrossRef.
DOI: https://doi.org/10.21705/ijbcs.v1i1.755
Refbacks
- There are currently no refbacks.
Copyright (c) 2026 Indonesian Journal of Basic and Clinical Studies

This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.
Managed by The Prodia Education and Research Institute