Cadmium delays puberty onset and testis growth in adolescents
Summary Objective Cadmium (Cd) has been shown to impair pubertal development in experimental animals. However, no data are available for male adolescents with increased urinary cadmium levels. Design The aim of this cross‐sectional study was to evaluate pubertal onset and pituitary–gonadal axis horm...
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Published in | Clinical endocrinology (Oxford) Vol. 83; no. 3; pp. 357 - 362 |
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Main Authors | , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
England
Blackwell Publishing Ltd
01.09.2015
Wiley Subscription Services, Inc |
Subjects | |
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Abstract | Summary
Objective
Cadmium (Cd) has been shown to impair pubertal development in experimental animals. However, no data are available for male adolescents with increased urinary cadmium levels.
Design
The aim of this cross‐sectional study was to evaluate pubertal onset and pituitary–gonadal axis hormones in male adolescents with increased urinary levels of Cd.
Subjects
We studied 111 males, aged 12–14 years living in the Milazzo‐Valle del Mela area. A control age‐matched population (n = 60) living 28–45 km far from the industrial site was also enrolled.
Measurements
Pubertal stages were assessed by clinical examination according to Tanner's score. Mean testicular volume was also investigated by ultrasound examination. Urinary Cd concentration and blood levels of FSH, LH, testosterone and inhibin B were also investigated.
Results
Cd levels were significantly higher in adolescents living in the Milazzo‐Valle del Mela area, compared to both age‐matched subjects living far from the industrial plants and the reference values. Our population showed also a delayed onset of puberty, a smaller testicular volume and lower testosterone levels. An inverse correlation was found between urinary Cd and testicular volume (r = −0·25; P = 0·0008), testosterone levels (Spearman's r = −0·0·37; two‐tailed P < 0·0001) and LH levels (Spearman's r = 0·048; P < 0·05). Testosterone levels were positively correlated with testicular volume (Spearman's r = 0·48; P < 0·0001).
Conclusions
This study, for the first time, suggests that increased Cd burden is associated with delayed onset of puberty in male adolescents and impaired testicular growth. |
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AbstractList | Cadmium (Cd) has been shown to impair pubertal development in experimental animals. However, no data are available for male adolescents with increased urinary cadmium levels.OBJECTIVECadmium (Cd) has been shown to impair pubertal development in experimental animals. However, no data are available for male adolescents with increased urinary cadmium levels.The aim of this cross-sectional study was to evaluate pubertal onset and pituitary-gonadal axis hormones in male adolescents with increased urinary levels of Cd.DESIGNThe aim of this cross-sectional study was to evaluate pubertal onset and pituitary-gonadal axis hormones in male adolescents with increased urinary levels of Cd.We studied 111 males, aged 12-14 years living in the Milazzo-Valle del Mela area. A control age-matched population (n = 60) living 28-45 km far from the industrial site was also enrolled.SUBJECTSWe studied 111 males, aged 12-14 years living in the Milazzo-Valle del Mela area. A control age-matched population (n = 60) living 28-45 km far from the industrial site was also enrolled.Pubertal stages were assessed by clinical examination according to Tanner's score. Mean testicular volume was also investigated by ultrasound examination. Urinary Cd concentration and blood levels of FSH, LH, testosterone and inhibin B were also investigated.MEASUREMENTSPubertal stages were assessed by clinical examination according to Tanner's score. Mean testicular volume was also investigated by ultrasound examination. Urinary Cd concentration and blood levels of FSH, LH, testosterone and inhibin B were also investigated.Cd levels were significantly higher in adolescents living in the Milazzo-Valle del Mela area, compared to both age-matched subjects living far from the industrial plants and the reference values. Our population showed also a delayed onset of puberty, a smaller testicular volume and lower testosterone levels. An inverse correlation was found between urinary Cd and testicular volume (r = -0·25; P = 0·0008), testosterone levels (Spearman's r = -0·0·37; two-tailed P < 0·0001) and LH levels (Spearman's r = 0·048; P < 0·05). Testosterone levels were positively correlated with testicular volume (Spearman's r = 0·48; P < 0·0001).RESULTSCd levels were significantly higher in adolescents living in the Milazzo-Valle del Mela area, compared to both age-matched subjects living far from the industrial plants and the reference values. Our population showed also a delayed onset of puberty, a smaller testicular volume and lower testosterone levels. An inverse correlation was found between urinary Cd and testicular volume (r = -0·25; P = 0·0008), testosterone levels (Spearman's r = -0·0·37; two-tailed P < 0·0001) and LH levels (Spearman's r = 0·048; P < 0·05). Testosterone levels were positively correlated with testicular volume (Spearman's r = 0·48; P < 0·0001).This study, for the first time, suggests that increased Cd burden is associated with delayed onset of puberty in male adolescents and impaired testicular growth.CONCLUSIONSThis study, for the first time, suggests that increased Cd burden is associated with delayed onset of puberty in male adolescents and impaired testicular growth. Cadmium (Cd) has been shown to impair pubertal development in experimental animals. However, no data are available for male adolescents with increased urinary cadmium levels. The aim of this cross-sectional study was to evaluate pubertal onset and pituitary-gonadal axis hormones in male adolescents with increased urinary levels of Cd. We studied 111 males, aged 12-14 years living in the Milazzo-Valle del Mela area. A control age-matched population (n = 60) living 28-45 km far from the industrial site was also enrolled. Pubertal stages were assessed by clinical examination according to Tanner's score. Mean testicular volume was also investigated by ultrasound examination. Urinary Cd concentration and blood levels of FSH, LH, testosterone and inhibin B were also investigated. Cd levels were significantly higher in adolescents living in the Milazzo-Valle del Mela area, compared to both age-matched subjects living far from the industrial plants and the reference values. Our population showed also a delayed onset of puberty, a smaller testicular volume and lower testosterone levels. An inverse correlation was found between urinary Cd and testicular volume (r = -0·25; P = 0·0008), testosterone levels (Spearman's r = -0·0·37; two-tailed P < 0·0001) and LH levels (Spearman's r = 0·048; P < 0·05). Testosterone levels were positively correlated with testicular volume (Spearman's r = 0·48; P < 0·0001). This study, for the first time, suggests that increased Cd burden is associated with delayed onset of puberty in male adolescents and impaired testicular growth. Summary Objective Cadmium (Cd) has been shown to impair pubertal development in experimental animals. However, no data are available for male adolescents with increased urinary cadmium levels. Design The aim of this cross‐sectional study was to evaluate pubertal onset and pituitary–gonadal axis hormones in male adolescents with increased urinary levels of Cd. Subjects We studied 111 males, aged 12–14 years living in the Milazzo‐Valle del Mela area. A control age‐matched population (n = 60) living 28–45 km far from the industrial site was also enrolled. Measurements Pubertal stages were assessed by clinical examination according to Tanner's score. Mean testicular volume was also investigated by ultrasound examination. Urinary Cd concentration and blood levels of FSH, LH, testosterone and inhibin B were also investigated. Results Cd levels were significantly higher in adolescents living in the Milazzo‐Valle del Mela area, compared to both age‐matched subjects living far from the industrial plants and the reference values. Our population showed also a delayed onset of puberty, a smaller testicular volume and lower testosterone levels. An inverse correlation was found between urinary Cd and testicular volume (r = −0·25; P = 0·0008), testosterone levels (Spearman's r = −0·0·37; two‐tailed P < 0·0001) and LH levels (Spearman's r = 0·048; P < 0·05). Testosterone levels were positively correlated with testicular volume (Spearman's r = 0·48; P < 0·0001). Conclusions This study, for the first time, suggests that increased Cd burden is associated with delayed onset of puberty in male adolescents and impaired testicular growth. Objective Cadmium (Cd) has been shown to impair pubertal development in experimental animals. However, no data are available for male adolescents with increased urinary cadmium levels. Design The aim of this cross-sectional study was to evaluate pubertal onset and pituitary-gonadal axis hormones in male adolescents with increased urinary levels of Cd. Subjects We studied 111 males, aged 12-14 years living in the Milazzo-Valle del Mela area. A control age-matched population (n = 60) living 28-45 km far from the industrial site was also enrolled. Measurements Pubertal stages were assessed by clinical examination according to Tanner's score. Mean testicular volume was also investigated by ultrasound examination. Urinary Cd concentration and blood levels of FSH, LH, testosterone and inhibin B were also investigated. Results Cd levels were significantly higher in adolescents living in the Milazzo-Valle del Mela area, compared to both age-matched subjects living far from the industrial plants and the reference values. Our population showed also a delayed onset of puberty, a smaller testicular volume and lower testosterone levels. An inverse correlation was found between urinary Cd and testicular volume (r = -0.25; P = 0.0008), testosterone levels (Spearman's r = -0.0.37; two-tailed P < 0.0001) and LH levels (Spearman's r = 0.048; P < 0.05). Testosterone levels were positively correlated with testicular volume (Spearman's r = 0.48; P < 0.0001). Conclusions This study, for the first time, suggests that increased Cd burden is associated with delayed onset of puberty in male adolescents and impaired testicular growth. Summary Objective Cadmium (Cd) has been shown to impair pubertal development in experimental animals. However, no data are available for male adolescents with increased urinary cadmium levels. Design The aim of this cross-sectional study was to evaluate pubertal onset and pituitary-gonadal axis hormones in male adolescents with increased urinary levels of Cd. Subjects We studied 111 males, aged 12-14 years living in the Milazzo-Valle del Mela area. A control age-matched population (n = 60) living 28-45 km far from the industrial site was also enrolled. Measurements Pubertal stages were assessed by clinical examination according to Tanner's score. Mean testicular volume was also investigated by ultrasound examination. Urinary Cd concentration and blood levels of FSH,LH, testosterone and inhibin B were also investigated. Results Cd levels were significantly higher in adolescents living in the Milazzo-Valle del Mela area, compared to both age-matched subjects living far from the industrial plants and the reference values. Our population showed also a delayed onset of puberty, a smaller testicular volume and lower testosterone levels. An inverse correlation was found between urinary Cd and testicular volume (r = -0·25; P = 0·0008), testosterone levels (Spearman's r = -0·0·37; two-tailed P < 0·0001) and LH levels (Spearman's r = 0·048; P < 0·05). Testosterone levels were positively correlated with testicular volume (Spearman's r = 0·48; P < 0·0001). Conclusions This study, for the first time, suggests that increased Cd burden is associated with delayed onset of puberty in male adolescents and impaired testicular growth. |
Author | Bitto, Alessandra Mecchio, Anna Pallio, Giovanni Luca, Filippo De Santamaria, Angelo Squadrito, Francesco Interdonato, Monica Irrera, Natasha Ramistella, Vincenzo Marini, Herbert Pizzino, Gabriele Altavilla, Domenica Minutoli, Letteria Galfo, Federica |
Author_xml | – sequence: 1 givenname: Monica surname: Interdonato fullname: Interdonato, Monica organization: Department of Clinical and Experimental Medicine, University of Messina, Messina, Italy – sequence: 2 givenname: Gabriele surname: Pizzino fullname: Pizzino, Gabriele organization: Department of Clinical and Experimental Medicine, University of Messina, Messina, Italy – sequence: 3 givenname: Alessandra surname: Bitto fullname: Bitto, Alessandra organization: Department of Clinical and Experimental Medicine, University of Messina, Messina, Italy – sequence: 4 givenname: Federica surname: Galfo fullname: Galfo, Federica organization: Department of Clinical and Experimental Medicine, University of Messina, Messina, Italy – sequence: 5 givenname: Natasha surname: Irrera fullname: Irrera, Natasha organization: Department of Clinical and Experimental Medicine, University of Messina, Messina, Italy – sequence: 6 givenname: Anna surname: Mecchio fullname: Mecchio, Anna organization: Department of Clinical and Experimental Medicine, University of Messina, Messina, Italy – sequence: 7 givenname: Giovanni surname: Pallio fullname: Pallio, Giovanni organization: Department of Clinical and Experimental Medicine, University of Messina, Messina, Italy – sequence: 8 givenname: Vincenzo surname: Ramistella fullname: Ramistella, Vincenzo organization: Department of Paediatric, Gynaecological, Microbiological and Biomedical Sciences, University of Messina, Messina, Italy – sequence: 9 givenname: Filippo De surname: Luca fullname: Luca, Filippo De organization: Department of Paediatric, Gynaecological, Microbiological and Biomedical Sciences, University of Messina, Messina, Italy – sequence: 10 givenname: Angelo surname: Santamaria fullname: Santamaria, Angelo organization: Department of Paediatric, Gynaecological, Microbiological and Biomedical Sciences, University of Messina, Messina, Italy – sequence: 11 givenname: Letteria surname: Minutoli fullname: Minutoli, Letteria organization: Department of Clinical and Experimental Medicine, University of Messina, Messina, Italy – sequence: 12 givenname: Herbert surname: Marini fullname: Marini, Herbert organization: Department of Clinical and Experimental Medicine, University of Messina, Messina, Italy – sequence: 13 givenname: Francesco surname: Squadrito fullname: Squadrito, Francesco email: Correspondence: Francesco Squadrito, Department of Clinical and Experimental Medicine, Section of Pharmacology, Torre Biologica 5 floor, c/o AOU "G. Martino", Via C. Valeria, 98125 Messina, Italy. Tel.: +390902213648; Fax: +390902213300; , fsquadrito@unime.it organization: Department of Clinical and Experimental Medicine, University of Messina, Messina, Italy – sequence: 14 givenname: Domenica surname: Altavilla fullname: Altavilla, Domenica organization: Department of Paediatric, Gynaecological, Microbiological and Biomedical Sciences, University of Messina, Messina, Italy |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/25521350$$D View this record in MEDLINE/PubMed |
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An update of recent studies and potential therapeutic approaches publication-title: Food and Chemical Toxicology – volume: 51 start-page: 170 year: 1976 end-page: 179 article-title: Clinical longitudinal standards for height, weight, height velocity, weight velocity, and stages of puberty publication-title: Archives of Disease in Childhood – volume: 2013 start-page: 898034 year: 2013 article-title: Cadmium and its neurotoxic effects publication-title: Oxidative Medicine and Cellular Longevity – volume: 13 start-page: 443 year: 1999 end-page: 449 article-title: Fertility of rabbit sperm exposed in vitro to cadmium and lead publication-title: Reproductive Toxicology – year: 2010 – volume: 146 start-page: 175 year: 2004 end-page: 182 article-title: Cadmium exposure differentially modifies the circadian patterns of norepinephrine at the median eminence and plasma LH, FSH and testosterone levels publication-title: Toxicology Letters – volume: 226 start-page: 605 year: 2001 end-page: 611 article-title: Cadmium effects on hypothalamic‐pituitary‐testicular axis in male rats publication-title: Experimental Biology and Medicine – volume: 90 start-page: 2077 year: 2013 end-page: 2084 article-title: Exposure to cadmium in male urban and rural workers and effects on FSH, LH and testosterone publication-title: Chemosphere – volume: 57 start-page: 265 year: 2013 end-page: 272 article-title: Causes and consequences of apoptosis in spermatozoa; contributions to infertility and impacts on development publication-title: International Journal of Developmental Biology – year: 2002 – volume: 2013 start-page: 394652 year: 2013 article-title: Cadmium toxicity and treatment publication-title: Scientific World Journal – volume: 205 start-page: 501 year: 2002 end-page: 503 article-title: Susceptibility of children to environmental toxic substances publication-title: International Journal of Hygiene and Environmental Health – volume: 43 start-page: 389 year: 2006 end-page: 397 article-title: Calculated free testosterone in men: comparison of four equations and with free androgen index publication-title: Annals of clinical biochemistry – volume: 38 start-page: 913 year: 2000 end-page: 923 article-title: Pubertal and postpubertal cadmium exposure differentially affects the hypothalamic‐pituitary‐testicular axis function in the rat publication-title: Food and Chemical Toxicology – volume: 19 start-page: 335 year: 2005 end-page: 349 article-title: Biological markers for metal toxicity publication-title: Environmental Toxicology and Pharmacology – volume: 172 start-page: 353 year: 2011 end-page: 365 article-title: Characterization of soil heavy metal contamination and potential health risk in metropolitan region of northern China publication-title: Environmental Monitoring and Assessment – volume: 82 start-page: 3976 year: 1997 end-page: 3981 article-title: Serum inhibin B in healthy pubertal and adolescent boys: relation to age, stage of puberty, and follicle‐stimulating hormone, luteinizing hormone, testosterone, and estradiol levels publication-title: Journal of Clinical Endocrinology and Metabolism. – ident: e_1_2_6_8_1 doi: 10.1016/j.fct.2013.06.024 – ident: e_1_2_6_6_1 doi: 10.1007/s10661-010-1339-1 – ident: e_1_2_6_5_1 doi: 10.1007/s00244-009-9417-5 – ident: e_1_2_6_11_1 doi: 10.1155/2014/326845 – ident: e_1_2_6_13_1 doi: 10.1136/adc.51.3.170 – ident: e_1_2_6_10_1 doi: 10.1016/j.chemosphere.2012.10.060 – volume-title: 2000 CDC growth charts for the United States: Methods and development year: 2002 ident: e_1_2_6_14_1 – ident: e_1_2_6_29_1 doi: 10.1210/jc.82.12.3976 – ident: e_1_2_6_25_1 doi: 10.1016/S0890-6238(99)00045-3 – ident: e_1_2_6_12_1 doi: 10.1016/j.redox.2014.05.003 – ident: e_1_2_6_7_1 doi: 10.1387/ijdb.130146ja – ident: e_1_2_6_2_1 doi: 10.1016/j.jtemb.2010.01.002 – volume: 26 start-page: 769 year: 2013 ident: e_1_2_6_21_1 article-title: Effect of cadmium on rat Leydig cell testosterone production and DNA integrity in vitro publication-title: Biomedical and Environmental Sciences – ident: e_1_2_6_24_1 doi: 10.1155/2013/898034 – ident: e_1_2_6_28_1 doi: 10.1016/S0378-4274(99)00159-9 – ident: e_1_2_6_18_1 doi: 10.1155/2013/394652 – ident: e_1_2_6_17_1 doi: 10.1016/j.ijheh.2012.01.003 – ident: e_1_2_6_16_1 – ident: e_1_2_6_20_1 doi: 10.1016/j.reprotox.2009.10.014 – ident: e_1_2_6_4_1 doi: 10.1210/er.2009-0002 – ident: e_1_2_6_19_1 doi: 10.1078/1438-4639-00179 – ident: e_1_2_6_3_1 doi: 10.1016/j.etap.2004.09.003 – ident: e_1_2_6_23_1 doi: 10.2131/jts.38.145 – ident: e_1_2_6_27_1 doi: 10.1016/j.toxlet.2003.10.004 – ident: e_1_2_6_26_1 doi: 10.1177/153537020122600615 – ident: e_1_2_6_9_1 doi: 10.1016/S0278-6915(00)00077-6 – ident: e_1_2_6_15_1 – volume: 27 start-page: 805 year: 2013 ident: e_1_2_6_22_1 article-title: Toxicity of cadmium on Sertoli cell functional competence: an in vitro study publication-title: Journal of Biological Regulators & Homeostatic Agents – ident: e_1_2_6_30_1 doi: 10.1258/000456306778520115 |
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Cadmium (Cd) has been shown to impair pubertal development in experimental animals. However, no data are available for male adolescents with... Cadmium (Cd) has been shown to impair pubertal development in experimental animals. However, no data are available for male adolescents with increased urinary... Summary Objective Cadmium (Cd) has been shown to impair pubertal development in experimental animals. However, no data are available for male adolescents with... Objective Cadmium (Cd) has been shown to impair pubertal development in experimental animals. However, no data are available for male adolescents with... |
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SubjectTerms | Adolescent Cadmium - urine Child Cross-Sectional Studies Follicle Stimulating Hormone - blood Humans Inhibins - blood Linear Models Luteinizing Hormone - blood Male Organ Size - physiology Puberty - blood Puberty - physiology Puberty - urine Testis - growth & development Testosterone - blood Time Factors Urban Health - statistics & numerical data Urban Population - statistics & numerical data |
Title | Cadmium delays puberty onset and testis growth in adolescents |
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