Literature DB >> 23520400

Association of placenta organotin concentrations with congenital cryptorchidism and reproductive hormone levels in 280 newborn boys from Denmark and Finland.

Panu Rantakokko1, Katharina M Main, Christine Wohlfart-Veje, Hannu Kiviranta, Riikka Airaksinen, Terttu Vartiainen, Niels E Skakkebæk, Jorma Toppari, Helena E Virtanen.   

Abstract

STUDY QUESTION: Is the placental burden of organotin compounds (OTCs) associated with congenital cryptorchidism in infant offspring from Finland and Denmark? SUMMARY ANSWER: Increasing concentrations of OTCs had a negative association with cryptorchidism in Finland, whereas a positive association was found in Denmark. WHAT IS KNOWN ALREADY: The rapid increase in the prevalence of cryptorchidism suggests that environmental factors, such as endocrine disruptors, may be involved. OTCs are endocrine disruptors at very low concentrations due to activation of the retinoid X receptor (RXR). STUDY DESIGN, SIZE, DURATION: Between the years 1997 and 2001, placentas from mothers of cryptorchid boys and from healthy controls were collected from Denmark (39 cases, 129 controls) and Finland (56 cases, 56 controls). In Denmark 33 and 6 boys, and in Finland 22 and 34 boys had mild or severe cryptorchidism, respectively. The association between concentrations of four OTCs [monobutyltin (MBT), dibutyltin (DBT), tributyltin (TBT) and triphenyltin (TPhT)] and case-control status was estimated. PARTICIPANTS/MATERIALS, SETTING,
METHODS: In both countries, placenta samples were selected from larger cohorts. In Finland placenta samples were collected from boys with cryptorchidism at birth and matched controls (nested case-control design). Matching criteria were parity, maternal smoking (yes/no), diabetes (yes/no), gestational age (±7 days) and date of birth (±14 days). Numbers of controls per case was 1. In Denmark, all available placentas from cryptorchid boys were chosen and control placentas were selected randomly from the total Danish cohort (case-cohort design). The average number of controls per case was 3.3. OTCs in placenta samples were analysed with liquid extraction, ethylation and gas chromatography-mass spectrometry determination and coded by country-specific tertiles. MAIN RESULTS AND THE ROLE OF CHANCE: Generally, the concentrations of OTCs were very low. For most analytes, a large proportion of samples (29-96% depending on the country and case-control status) had OTC concentrations below the limit of quantification (LOQ). As an exception, the concentration of TBT was >LOQ in 99% of Finnish placentas. The mean concentrations of DBT and TBT were 1.5 and 7 times higher in Finland than in Denmark, respectively. For DBT in Danish placentas, the odds ratio (OR) for cryptorchidism in the second tertile (0.10-0.14 ng/g) when compared with the first tertile (<0.10 ng/g, <LOQ) was 3.13 (95% CI 1.19-8.26) and the OR for the third tertile (≥0.15 ng/g) when compared with the first tertile was 4.01 (95% CI 1.42-11.33). For TBT in Finnish placentas, the OR for cryptorchidism in the second tertile (0.10-0.39 ng/g) when compared with the first tertile (<0.1 ng/g) was 0.61 (95% CI 0.18-2.01) and the OR for the third tertile (≥0.40 ng/g) when compared with the first tertile was 0.13 (95% CI 0.03-0.54). LIMITATIONS, REASONS FOR CAUTION: The main limitation of the study was the relatively small number of mother-boy pairs that limits the extrapolation of the study results to the general population. Also misclassification of exposure is a reason for caution for two reasons: because the concentrations of most OTCs were below or only barely above the LOQ in a large proportion of samples and because it is not known how well OTCs measured from placenta represent exposure at the time window that is relevant for cryptorchidism occurrence. WIDER IMPLICATIONS OF THE
FINDINGS: This is the first study to measure the concentrations of OTCs from human placenta samples, and to associate these concentrations to cryptorchidism. As opposite results were obtained with regard to OTC concentration in placenta and cryptorchidism status in Finland and Denmark, and no mechanism is known at the moment by which OTCs could affect testicular descent, these results cannot be generalized to other populations. However, some animal tests described in the literature show opposite effects of OTCs on fat deposition at different ranges of exposure. It is also clearly shown in the literature that TBT has an impact on sexual development of gastropods through RXR. As TBT is known to activate human RXR, further laboratory studies should be designed to explore the potential impact of TBT on male sexual development.

Entities:  

Keywords:  cryptorchidism; infant; organotin compounds; placenta; tributyltin

Mesh:

Substances:

Year:  2013        PMID: 23520400     DOI: 10.1093/humrep/det040

Source DB:  PubMed          Journal:  Hum Reprod        ISSN: 0268-1161            Impact factor:   6.918


  11 in total

Review 1.  Risk factors for cryptorchidism.

Authors:  Jason K Gurney; Katherine A McGlynn; James Stanley; Tony Merriman; Virginia Signal; Caroline Shaw; Richard Edwards; Lorenzo Richiardi; John Hutson; Diana Sarfati
Journal:  Nat Rev Urol       Date:  2017-06-27       Impact factor: 14.432

2.  Levels of tin and organotin compounds in human urine samples from Iowa, United States.

Authors:  Manuel Gadogbe; Wei Bao; Brian R Wels; Suzie Y Dai; Donna A Santillan; Mark K Santillan; Hans-Joachim Lehmler
Journal:  J Environ Sci Health A Tox Hazard Subst Environ Eng       Date:  2019-05-06       Impact factor: 2.269

Review 3.  Possible fetal determinants of male infertility.

Authors:  Anders Juul; Kristian Almstrup; Anna-Maria Andersson; Tina K Jensen; Niels Jørgensen; Katharina M Main; Ewa Rajpert-De Meyts; Jorma Toppari; Niels E Skakkebæk
Journal:  Nat Rev Endocrinol       Date:  2014-06-17       Impact factor: 43.330

4.  Environmental tin exposure in a nationally representative sample of U.S. adults and children: The National Health and Nutrition Examination Survey 2011-2014.

Authors:  Hans-Joachim Lehmler; Manuel Gadogbe; Buyun Liu; Wei Bao
Journal:  Environ Pollut       Date:  2018-05-12       Impact factor: 8.071

Review 5.  EDC-2: The Endocrine Society's Second Scientific Statement on Endocrine-Disrupting Chemicals.

Authors:  A C Gore; V A Chappell; S E Fenton; J A Flaws; A Nadal; G S Prins; J Toppari; R T Zoeller
Journal:  Endocr Rev       Date:  2015-11-06       Impact factor: 19.871

6.  Insights into the Evolution of Spermatogenesis-Related Ubiquitin-Proteasome System Genes in Abdominal Testicular Laurasiatherians.

Authors:  Xiaoyue Ding; Li Cao; Yu Zheng; Xu Zhou; Xiaofang He; Shixia Xu; Wenhua Ren
Journal:  Genes (Basel)       Date:  2021-11-10       Impact factor: 4.096

Review 7.  Praegnatio Perturbatio-Impact of Endocrine-Disrupting Chemicals.

Authors:  Vasantha Padmanabhan; Wenhui Song; Muraly Puttabyatappa
Journal:  Endocr Rev       Date:  2021-05-25       Impact factor: 19.871

8.  Association of placenta organotin concentrations with growth and ponderal index in 110 newborn boys from Finland during the first 18 months of life: a cohort study.

Authors:  Panu Rantakokko; Katharina M Main; Christine Wohlfart-Veje; Hannu Kiviranta; Riikka Airaksinen; Terttu Vartiainen; Niels E Skakkebæk; Jorma Toppari; Helena E Virtanen
Journal:  Environ Health       Date:  2014-06-05       Impact factor: 5.984

Review 9.  Organotin Exposure and Vertebrate Reproduction: A Review.

Authors:  Julia Fernandez Puñal de Araújo; Priscila Lang Podratz; Eduardo Merlo; Isabela Valim Sarmento; Charles Santos da Costa; Oscar Mauricio Santamaria Niño; Rodrigo Alves Faria; Leandro Ceotto Freitas Lima; Jones Bernardes Graceli
Journal:  Front Endocrinol (Lausanne)       Date:  2018-03-01       Impact factor: 5.555

Review 10.  The Impact of Endocrine-Disrupting Chemicals in Male Fertility: Focus on the Action of Obesogens.

Authors:  Luís Rato; Ana C A Sousa
Journal:  J Xenobiot       Date:  2021-11-29
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