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1.
Hum Reprod ; 28(1): 274-82, 2013 Jan.
Article in English | MEDLINE | ID: mdl-23042799

ABSTRACT

BACKGROUND: Older men tend to have poorer semen quality and are generally at higher risks for infertility and abnormal reproductive outcomes. METHODS: We employed proton-induced X-ray emission (PIXE, 3 MeV proton beam) to investigate the concentrations of zinc, copper, calcium, sulfur, chlorine, potassium, titanium, iron and nickel in washed sperm and seminal plasma from non-smoking groups of 10 older men (65-80 years old) and 10 younger men (22-28 years old) who were concurrently assayed for sperm function and genomicly defective sperm. RESULTS: The older group showed elevated zinc, copper and calcium in sperm and elevated sulfur in seminal plasma compared with the younger men. The older group also showed reduced motility as well as increased sperm DNA fragmentation, achondroplasia mutations, DNA strand breaks and chromosomal aberrations. Sperm calcium and copper were positively associated with sperm DNA fragmentation (P < 0.03). Seminal sulfur was positively associated with sperm DNA fragmentation and chromosomal aberrations (P < 0.04), and negatively associated with sperm motility (P < 0.05). Sperm calcium was negatively associated with sperm motility, independent of male age (P = 0.01). CONCLUSIONS: We identified major differences in elemental concentrations between sperm and seminal plasma and that higher sperm copper, sulfur and calcium are quantitatively associated with poorer semen quality and increased frequencies of genomic sperm defects.


Subject(s)
Aging , Genetic Variation , Semen/chemistry , Sperm Motility , Spermatozoa/chemistry , Trace Elements/analysis , Adult , Aged , Aged, 80 and over , Chromosome Aberrations , Cohort Studies , DNA Breaks, Single-Stranded , DNA Fragmentation , Humans , Male , Microscopy, Electron, Scanning Transmission , Mutation , Pilot Projects , Semen/metabolism , Spectrometry, X-Ray Emission , Spermatozoa/metabolism , Trace Elements/metabolism , Young Adult
2.
Fertil Steril ; 98(5): 1130-7.e1, 2012 Nov.
Article in English | MEDLINE | ID: mdl-22935557

ABSTRACT

OBJECTIVE: To investigate whether lifestyle factors such as increased dietary intake of micronutrients reduce the risks of sperm DNA damage, and whether older men benefit more than younger men. DESIGN: Cross-sectional study design with equalized assignments into age groups. SETTING: National laboratory and university. PATIENT(S): Nonclinical group of 22-80-year-old nonsmoking men (n = 80) who reported no fertility problems. MAIN OUTCOME MEASURE(S): Sperm DNA damage measured by alkaline and neutral DNA electrophoresis (i.e., sperm Comet assay). RESULT(S): Sociodemographics, occupational exposures, medical and reproductive histories, and lifestyle habits were determined by questionnaire. The average daily dietary and supplement intake of micronutrients (vitamin C, vitamin E, b-carotene, zinc, and folate) was determined using the 100-item Modified Block Food Frequency Questionnaire (FFQ). Men with the highest intake of vitamin C had approximately 16% less sperm DNA damage (alkaline sperm Comet) than men with the lowest intake, with similar findings for vitamin E, folate, and zinc (but not ß-carotene). Older men (>44 years) with the highest vitamin C intake had approximately 20% less sperm DNA damage compared with older men with the lowest intake, with similar findings for vitamin E and zinc. The older men with the highest intake of these micronutrients showed levels of sperm damage that were similar to those of the younger men. However, younger men (<44 years) did not benefit from higher intakes of the micronutrients surveyed. CONCLUSION(S): Men with higher dietary and supplement intake of certain micronutrients may produce sperm with less DNA damage, especially among older men. This raises the broader question of how lifestyle factors, including higher intakes of antioxidants and micronutrients, might protect somatic as well as germ cells against age-associated genomic damage.


Subject(s)
Aging/genetics , DNA Damage , Micronutrients/administration & dosage , Spermatozoa/drug effects , Adult , Age Factors , Aged , Aged, 80 and over , Aging/pathology , Antioxidants/administration & dosage , California , Comet Assay , Cross-Sectional Studies , Diet , Dietary Supplements , Humans , Life Style , Linear Models , Male , Middle Aged , Multivariate Analysis , Nutrition Assessment , Semen Analysis/methods , Spermatozoa/chemistry , Spermatozoa/pathology , Surveys and Questionnaires , Vitamins/administration & dosage , Young Adult , Zinc/administration & dosage
3.
Environ Mol Mutagen ; 53(3): 218-26, 2012 Apr.
Article in English | MEDLINE | ID: mdl-22351378

ABSTRACT

Benzene is a primary industrial chemical and a ubiquitous environmental pollutant that causes human leukemia and maybe other malignancies. Occupational exposure to benzene has been associated with increased chromosomal aneuploidies in blood lymphocytes and, in separate studies, in sperm. However, aneuploidy detection in somatic and germ cells within the same benzene-exposed individuals has never been reported. To compare aneuploidies in blood lymphocytes and sperm within the same individuals exposed to benzene, a cross-sectional study was conducted in 33 benzene-exposed male workers and 33 unexposed workers from Chinese factories. Air benzene concentrations in the exposed workers ranged from below the detection limit to 24 ppm (median, 2.9 ppm) and were undetectable in the unexposed subjects. Aneuploidies of chromosomes 21, X, and Y in blood lymphocytes were examined by multicolor fluorescence in situ hybridization and were compared to the previously reported aneuploidies in sperm. The results showed that benzene exposure was positively associated with the gain of chromosome 21 but not sex chromosomes in blood lymphocytes. This was in contrast to analysis of sperm, where the gain of sex chromosomes, but not chromosome 21, was significantly increased in the exposed workers. Furthermore, a significant correlation in the gain of sex chromosomes between blood lymphocytes and sperm was observed among the unexposed subjects, but not among the exposed workers. The findings suggest that benzene exposure induces aneuploidies in both blood cells and sperm within the same individuals, but selectively affects chromosome 21 in blood lymphocytes and the sex chromosomes in sperm.


Subject(s)
Aneuploidy , Benzene/toxicity , Chromosomes, Human, Pair 21/drug effects , Chromosomes, Human, X/drug effects , Chromosomes, Human, Y/drug effects , Environmental Pollutants/toxicity , Lymphocytes/drug effects , Occupational Exposure/adverse effects , Spermatozoa/drug effects , Air Pollutants/adverse effects , China , Cross-Sectional Studies , Humans , Male
4.
Environ Health Perspect ; 120(2): 229-34, 2012 Feb.
Article in English | MEDLINE | ID: mdl-22086566

ABSTRACT

BACKGROUND: Benzene is an industrial chemical that causes blood disorders, including acute myeloid leukemia. We previously reported that occupational exposures near the U.S. Occupational Safety and Health Administration permissible exposure limit (8 hr) of 1 ppm was associated with sperm aneuploidy. OBJECTIVE: We investigated whether occupational exposures near 1 ppm increase the incidence of sperm carrying structural chromosomal aberrations. METHODS: We applied a sperm fluorescence in situ hybridization assay to measure frequencies of sperm carrying partial chromosomal duplications or deletions of 1cen or 1p36.3 or breaks within 1cen-1q12 among 30 benzene-exposed and 11 unexposed workers in Tianjin, China, as part of the China Benzene and Sperm Study (C-BASS). Exposed workers were categorized into low-, moderate-, and high-exposure groups based on urinary benzene (medians: 2.9, 11.0, and 110.6 µg/L, respectively). Median air benzene concentrations in the three exposure groups were 1.2, 3.7, and 8.4 ppm, respectively. RESULTS: Adjusted incidence rate ratios (IRRs) and 95% confidence intervals (CIs) for all structural aberrations combined were 1.42 (95% CI: 1.10, 1.83), 1.44 (95% CI: 1.12, 1.85), and 1.75 (95% CI: 1.36, 2.24) and for deletion of 1p36.3 alone were 4.31 (95% CI: 1.18, 15.78), 6.02 (95% CI: 1.69, 21.39), and 7.88 (95% CI: 2.21, 28.05) for men with low, moderate, and high exposure, respectively, compared with unexposed men. Chromosome breaks were significantly increased in the high-exposure group [IRR 1.49 (95% CI: 1.10, 2.02)]. CONCLUSIONS: Occupational exposures to benzene were associated with increased incidence of chromosomally defective sperm, raising concerns for worker infertility and spontaneous abortions as well as mental retardation and inherited defects in their children. Our sperm findings point to benzene as a possible risk factor for de novo 1p36 deletion syndrome. Because chromosomal aberrations in sperm can arise from defective stem cells/spermatogonia, our findings raise concerns that occupational exposure to benzene may have persistent reproductive effects in formerly exposed workers.


Subject(s)
Benzene/toxicity , Chromosome Aberrations/chemically induced , Environmental Pollutants/toxicity , Occupational Exposure , Spermatozoa/drug effects , Adult , Benzene/analysis , Benzene/standards , China , Dose-Response Relationship, Drug , Environmental Pollutants/standards , Environmental Pollutants/urine , Humans , In Situ Hybridization, Fluorescence , Male , Middle Aged , Sorbic Acid/analogs & derivatives , Sorbic Acid/analysis , Young Adult
5.
J Environ Public Health ; 2010: 861757, 2010.
Article in English | MEDLINE | ID: mdl-20671963

ABSTRACT

BACKGROUND: Research suggests that estrogenic endocrine-disrupting chemicals interfere with lactation. OBJECTIVES: (1) to determine if estrogenic persistent organic pollutants (POPs) are associated with shortened lactation duration; (2) to determine whether previous breastfeeding history biases associations. METHODS AND RESULTS: We measured selected organochlorines and polychlorinated biphenyls (p, p'-DDE, p, p'-DDT, o, p'-DDT, beta-hexachlorocyclohexane, hexachlorobenzene, and PCBs 44, 49, 52, 118, 138, 153, and 180) in serum from 366 low-income, Mexican-American pregnant women living in an agricultural region of California and assessed breastfeeding duration by questionnaires. We found no association between DDE, DDT, or estrogenic POPs with shortened lactation duration, but rather associations for two potentially estrogenic POPs with lengthened lactation duration arose (HR [95% CI]: 0.6 [0.4, 0.8] for p, p'-DDE & 0.8 [0.6, 1.0] for PCB 52). Associations between antiestrogenic POPs (PCBs 138 and 180) and shortened lactation duration were attributed to a lactation history bias. CONCLUSION: Estrogenic POPs were not associated with shortened lactation duration, but may be associated with longer lactation duration.


Subject(s)
Endocrine Disruptors/toxicity , Estrogens/toxicity , Hydrocarbons, Chlorinated/toxicity , Lactation/drug effects , Mexican Americans , Polychlorinated Biphenyls/toxicity , Adolescent , Adult , California , Endocrine Disruptors/blood , Estrogens/blood , Female , Humans , Hydrocarbons, Chlorinated/blood , Kaplan-Meier Estimate , Lactation/blood , Lactation/ethnology , Longitudinal Studies , Middle Aged , Pesticides/blood , Pesticides/toxicity , Polychlorinated Biphenyls/blood , Pregnancy , Principal Component Analysis , Proportional Hazards Models , Self Report , Time Factors , Young Adult
6.
Environ Health Perspect ; 118(6): 833-9, 2010 Jun.
Article in English | MEDLINE | ID: mdl-20418200

ABSTRACT

BACKGROUND: Benzene is a common industrial chemical known to induce leukemia and other blood disorders, as well as aneuploidy, in both human blood cells and sperm at exposures > 10 ppm. Recent reports have identified health effects at exposure levels < 1 ppm, the permissible exposure limit (PEL; 8 hr) set by the U.S. Occupational Safety and Health Administration. OBJECTIVE: We investigated whether occupational exposures to benzene near 1 ppm induce aneuploidy in sperm. METHODS: We used multicolor fluorescence in situ hybridization to measure the incidence of sperm with numerical abnormalities of chromosomes X, Y, and 21 among 33 benzene-exposed men and 33 unexposed men from Chinese factories. Individual exposures were assessed using personal air monitoring and urinary concentrations of benzene and trans,trans-muconic acid (E,E-MA). Air benzene concentrations were not detectable in unexposed men; in exposed men, concentrations ranged from below the detection limit to 24 ppm (median, 2.9 ppm), with 27% of exposed men (n = 9) having concentrations of

Subject(s)
Aneuploidy , Benzene/toxicity , Chromosome Aberrations/chemically induced , Environmental Pollutants/toxicity , Occupational Exposure/analysis , Spermatozoa/drug effects , Benzene/analysis , China , Environmental Pollutants/standards , Environmental Pollutants/urine , Humans , In Situ Hybridization, Fluorescence , Male , Sorbic Acid/analogs & derivatives , Sorbic Acid/analysis
7.
Fertil Steril ; 87(5): 1077-86, 2007 May.
Article in English | MEDLINE | ID: mdl-17433321

ABSTRACT

OBJECTIVE: To investigate the association between male age and the frequency of sperm with de novo structural chromosomal abnormalities. DESIGN: Semen specimens collected from two groups of 10 healthy, nonsmoking men, aged 22-28 and 65-80 years, were analyzed with the use of a multicolor fluorescence in situ hybridization assay for detecting breaks, segmental duplications and deletions, and aneuploidy and diploidy involving chromosome 1. SETTING: Healthy volunteer workers and retirees from a government research environment. MAIN OUTCOME MEASURE: Sperm carrying numerical and structural chromosomal abnormalities. RESULT(S): We detected significant increases in the frequency of sperm carrying breaks and segmental duplications and deletions of chromosome 1 among older men compared with younger men. Older men carried twice the frequency of sperm with segmental duplications and deletions of chromosome 1. The frequency of sperm carrying breaks within the 1q12 fragile-site region nearly doubled in older men. In contrast to female gametes, there was no effect of age on the frequency of sperm with numerical chromosomal abnormalities. CONCLUSION: Our findings suggest that advancing male age is associated with a gradual and significant increase in the risk of fathering children with various chromosomal defects such as segmental aneusomy syndromes.


Subject(s)
Aging/genetics , Aging/pathology , Chromosome Aberrations , Chromosomes, Human, Pair 1/genetics , Spermatozoa/physiology , Adult , Aged , Aged, 80 and over , Gene Deletion , Gene Duplication , Humans , Male , Spermatozoa/pathology
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