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1.
PLoS One ; 19(5): e0303115, 2024.
Article in English | MEDLINE | ID: mdl-38776353

ABSTRACT

The detrimental effects of ultraviolet C (UVC) radiation on living organisms, with a specific focus on the fruit fly Drosophila melanogaster, were examined. This study investigated the impact of heightened UVC radiation exposure on D. melanogaster by assessing mortality and fertility rates, studying phenotypic mutations, and investigating the associated molecular mechanisms. The findings of this study revealed that UVC radiation increases mortality rates and decreases fertility rates in D. melanogaster. Additionally, phenotypic wing mutations were observed in the exposed flies. Furthermore, the study demonstrated that UVC radiation downregulates the expression of antioxidant genes, including superoxide dismutase (SOD), manganese-dependent superoxide dismutase (Mn-SOD), zinc-dependent superoxide dismutase (Cu-Zn-SOD), and the G protein-coupled receptor methuselah (MTH) gene. These results suggest that UVC radiation exerts a destructive effect on D. melanogaster by inducing oxidative stress, which is marked by the overexpression of harmful oxidative processes and a simultaneous reduction in antioxidant gene expression. In conclusion, this study underscores the critical importance of comprehending the deleterious effects of UVC radiation, not only to safeguard human health on Earth, but also to address the potential risks associated with space missions, such as the ongoing Emirate astronaut program.


Subject(s)
Drosophila melanogaster , Fertility , Mutation , Ultraviolet Rays , Animals , Drosophila melanogaster/radiation effects , Drosophila melanogaster/genetics , Ultraviolet Rays/adverse effects , Fertility/radiation effects , Fertility/genetics , Mutation/radiation effects , Drosophila Proteins/genetics , Drosophila Proteins/metabolism , Oxidative Stress/radiation effects , Oxidative Stress/genetics , Male , Female , Superoxide Dismutase/genetics , Superoxide Dismutase/metabolism , Antioxidants/metabolism , Gene Expression Regulation/radiation effects
2.
Int J Mol Sci ; 25(9)2024 Apr 24.
Article in English | MEDLINE | ID: mdl-38731841

ABSTRACT

Plutella xylostella (Linnaeus) mainly damages cruciferous crops and causes huge economic losses. Presently, chemical pesticides dominate its control, but prolonged use has led to the development of high resistance. In contrast, the sterile insect technique provides a preventive and control method to avoid the development of resistance. We discovered two genes related to the reproduction of Plutella xylostella and investigated the efficacy of combining irradiation with RNA interference for pest management. The results demonstrate that after injecting PxAKT and PxCDK5, there was a significant decrease of 28.06% and 25.64% in egg production, and a decrease of 19.09% and 15.35% in the hatching rate compared to the control. The ratio of eupyrene sperm bundles to apyrene sperm bundles also decreased. PxAKT and PxCDK5 were identified as pivotal genes influencing male reproductive processes. We established a dose-response relationship for irradiation (0-200 Gy and 200-400 Gy) and derived the irradiation dose equivalent to RNA interference targeting PxAKT and PxCDK5. Combining RNA interference with low-dose irradiation achieved a sub-sterile effect on Plutella xylostella, surpassing either irradiation or RNA interference alone. This study enhances our understanding of the genes associated with the reproduction of Plutella xylostella and proposes a novel approach for pest management by combining irradiation and RNA interference.


Subject(s)
Cyclin-Dependent Kinase 5 , Proto-Oncogene Proteins c-akt , RNA Interference , Animals , Male , Proto-Oncogene Proteins c-akt/metabolism , Proto-Oncogene Proteins c-akt/genetics , Cyclin-Dependent Kinase 5/genetics , Cyclin-Dependent Kinase 5/metabolism , Fertility/radiation effects , Fertility/genetics , Moths/genetics , Insect Proteins/genetics , Insect Proteins/metabolism , Female , Reproduction/radiation effects , Reproduction/genetics
3.
Sci Rep ; 13(1): 15671, 2023 09 21.
Article in English | MEDLINE | ID: mdl-37735181

ABSTRACT

Sperm quality can be easily influenced by living environmental and occupational factors. This study aimed to discover potential semen quality related living environmental and occupational factors, expand knowledge of risk factors for semen quality, strengthen men's awareness of protecting their own fertility and assist the clinicians to judge the patient's fertility. 465 men without obese or underweight (18.5 < BMI < 28.5 kg/m2), long-term medical history and history of drug use, were recruited between June 2020 to July 2021, they are in reproductive age (25 < age < 45 years). We have collected their semen analysis results and clinical information. Logistic regression was applied to evaluate the association of semen quality with different factors. We found that living environment close to high voltage line (283.4 × 106/ml vs 219.8 × 106/ml, Cohen d = 0.116, P = 0.030) and substation (309.1 × 106/ml vs 222.4 × 106/ml, Cohen d = 0.085, P = 0.015) will influence sperm count. Experienced decoration in the past 6 months was a significant factor to sperm count (194.2 × 106/ml vs 261.0 × 106/ml, Cohen d = 0.120, P = 0.025). Living close to chemical plant will affect semen PH (7.5 vs 7.2, Cohen d = 0.181, P = 0.001). Domicile close to a power distribution room will affect progressive sperm motility (37.0% vs 34.0%, F = 4.773, Cohen d = 0.033, P = 0.030). Using computers will affect both progressive motility sperm (36.0% vs 28.1%, t = 2.762, Cohen d = 0.033, P = 0.006) and sperm total motility (57.0% vs 41.0%, Cohen d = 0.178, P = 0.009). After adjust for potential confounding factors (age and BMI), our regression model reveals that living close to high voltage line is a risk factor for sperm concentration (Adjusted OR 4.03, 95% CI 1.15-14.18, R2 = 0.048, P = 0.030), living close to Chemical plants is a protective factor for sperm concentration (Adjusted OR 0.15, 95% CI 0.05-0.46, R2 = 0.048, P = 0.001) and total sperm count (Adjusted OR 0.36, 95% CI 0.13-0.99, R2 = 0.026, P = 0.049). Time spends on computer will affect sperm total motility (Adjusted OR 2.29, 95% CI 1.11-4.73, R2 = 0.041, P = 0.025). Sum up, our results suggested that computer using, living and working surroundings (voltage line, substation and chemical plants, transformer room), and housing decoration may association with low semen quality. Suggesting that some easily ignored factors may affect male reproductive ability. Couples trying to become pregnant should try to avoid exposure to associated risk factors. The specific mechanism of risk factors affecting male reproductive ability remains to be elucidated.


Subject(s)
East Asian People , Fertility , Neighborhood Characteristics , Semen Analysis , Social Determinants of Health , Working Conditions , Humans , Male , Middle Aged , Cross-Sectional Studies , Semen , Sperm Motility , Adult , Risk Factors , Fertility/drug effects , Fertility/radiation effects
4.
Int J Radiat Biol ; 99(3): 551-560, 2023.
Article in English | MEDLINE | ID: mdl-35675553

ABSTRACT

PURPOSE: To analyze the results of direct and transgenerational effects of radio frequency electromagnetic fields (RF-EMF) on the model organism of crustaceans Daphnia magna. MATERIALS AND METHODS: D. magna were chronically exposed at 900 GHz EMF with an energy flux density (EFD) of about 1 mW/cm2 in the juvenile and pubertal periods of their ontogenesis. The cytotoxicity of exposure as well as survival, fertility and teratogenic effect of directly exposed daphnids and their progeny across three generations were analyzed. RESULTS AND CONCLUSIONS: The results of our study show that exposure of RF-EMF at juvenile period can significantly affect the fertility and size of irradiated daphnids and their offspring of the first generation. The decrease in fertility may be associated with a cytotoxic effect on the cells of irradiated animals. The reduction in the size of the terminal spine and the body of individuals is an indicator of the negative impact of radiation on the protective strategy of the crustacean population. The reproductive process is restored by the second generation. The results of our study provide further insights into the possible mechanisms underlying the in vivo effects of RF-EMF.


Subject(s)
Daphnia , Sexual Maturation , Animals , Daphnia/radiation effects , Fertility/radiation effects , Electromagnetic Fields/adverse effects , Radio Waves/adverse effects , Reproduction
5.
Cancer Radiother ; 26(1-2): 417-423, 2022.
Article in English | MEDLINE | ID: mdl-34953688

ABSTRACT

We present the updated recommendations of the French society for radiation oncology on radiotherapy and pregnancy. The occurrence of cancer during pregnancy is a rare event (approximately 1 in 1000 pregnancies). The risks for the embryo or the foetus depend on the gestational age at the time of irradiation. The main risks are malformations with microcephaly and mental retardation. There is also a risk of radiation-induced cancer in the unborn child. In the case of only supradiaphragmatic irradiation, radiotherapy can be performed most often in pregnant women without risk to the foetus. On the other hand, in the case of an indication for subdiaphragmatic irradiation, therapeutic termination of the pregnancy should be proposed. In all cases, when radiotherapy is chosen, a phantom estimation of the dose delivered to the foetus, confirmed by in vivo measurement, is recommended. Conformational radiotherapy is the preferred technique because of the lower dose delivered to the foetus (except in tumour locations where other techniques such as IMRT are recommended).


Subject(s)
Pregnancy Complications, Neoplastic/radiotherapy , Abortion, Therapeutic , Female , Fertility/radiation effects , Fetus/radiation effects , France , Gestational Age , Humans , Intellectual Disability/etiology , Microcephaly/etiology , Neoplasms, Radiation-Induced/etiology , Pregnancy , Proton Therapy/methods , Radiation Dosage , Radiation Exposure/legislation & jurisprudence , Radiation Injuries/complications , Radiation Oncology , Radiotherapy, Conformal/methods
6.
Eur J Endocrinol ; 185(6): 775-782, 2021 Oct 21.
Article in English | MEDLINE | ID: mdl-34582359

ABSTRACT

CONTEXT: Whilst radioactive iodine (RAI) is often administered in the treatment for differentiated thyroid carcinoma (DTC), long-term data on male fertility after RAI are scarce. OBJECTIVE: To evaluate long-term male fertility after RAI for DTC, and to compare semen quality before and after RAI. DESIGN, SETTING, AND PATIENTS: Multicenter study including males with DTC ≥2 years after their final RAI treatment with a cumulative activity of ≥3.7 GBq. MAIN OUTCOME MEASURE(S): Semen analysis, hormonal evaluation, and a fertility-focused questionnaire. Cut-off scores for 'low semen quality' were based on reference values of the general population as defined by the World Health Organization (WHO). RESULTS: Fifty-one participants had a median age of 40.5 (interquartile range (IQR): 34.0-49.6) years upon evaluation and a median follow-up of 5.8 (IQR: 3.0-9.5) years after their last RAI administration. The median cumulative administered activity of RAI was 7.4 (range: 3.7-23.3) GBq. The proportion of males with a low semen volume, concentration, progressive motility, or total motile sperm count did not differ from the 10th percentile cut-off of a general population (P = 0.500, P = 0.131, P = 0.094, and P = 0.500, respectively). Cryopreserved semen was used by 1 participant of the 20 who had preserved semen. CONCLUSIONS: Participants had a normal long-term semen quality. The proportion of participants with low semen quality parameters scoring below the 10th percentile did not differ from the general population. Cryopreservation of semen of males with DTC is not crucial for conceiving a child after RAI administration but may be considered in individual cases.


Subject(s)
Fertility/radiation effects , Iodine Radioisotopes/administration & dosage , Sperm Count/trends , Thyroid Neoplasms/epidemiology , Thyroid Neoplasms/radiotherapy , Adult , Follow-Up Studies , Humans , Male , Middle Aged , Netherlands/epidemiology , Semen Analysis/methods , Semen Analysis/trends , Sperm Count/methods , Treatment Outcome
7.
Molecules ; 26(6)2021 Mar 17.
Article in English | MEDLINE | ID: mdl-33802807

ABSTRACT

Infertility is a potential side effect of radiotherapy and significantly affects the quality of life for adolescent cancer survivors. Very few studies have addressed in pubertal models the mechanistic events that could be targeted to provide protection from gonadotoxicity and data on potential radioprotective treatments in this peculiar period of life are elusive. In this study, we utilized an in vitro model of the mouse pubertal testis to investigate the efficacy of crocetin to counteract ionizing radiation (IR)-induced injury and potential underlying mechanisms. Present experiments provide evidence that exposure of testis fragments from pubertal mice to 2 Gy X-rays induced extensive structural and cellular damage associated with overexpression of PARP1, PCNA, SOD2 and HuR and decreased levels of SIRT1 and catalase. A twenty-four hr exposure to 50 µM crocetin pre- and post-IR significantly reduced testis injury and modulated the response to DNA damage and oxidative stress. Nevertheless, crocetin treatment did not counteract the radiation-induced changes in the expression of SIRT1, p62 and LC3II. These results increase the knowledge of mechanisms underlying radiation damage in pubertal testis and establish the use of crocetin as a fertoprotective agent against IR deleterious effects in pubertal period.


Subject(s)
Carotenoids/pharmacology , Fertility/drug effects , Puberty/drug effects , Radiation Injuries/drug therapy , Testis/drug effects , Vitamin A/analogs & derivatives , Animals , Autophagy/drug effects , Autophagy/radiation effects , Carotenoids/therapeutic use , Catalase/metabolism , Cells, Cultured , Down-Regulation , ELAV-Like Protein 1/metabolism , Fertility/radiation effects , Gene Expression Regulation, Developmental/drug effects , Gene Expression Regulation, Developmental/radiation effects , Immunohistochemistry , In Vitro Techniques , Male , Mice , Microtubule-Associated Proteins/metabolism , Oxidative Stress/drug effects , Oxidative Stress/radiation effects , Poly (ADP-Ribose) Polymerase-1/metabolism , Proliferating Cell Nuclear Antigen/metabolism , Puberty/radiation effects , Seminiferous Tubules/cytology , Seminiferous Tubules/drug effects , Seminiferous Tubules/radiation effects , Sirtuin 1/metabolism , Superoxide Dismutase/metabolism , Testis/radiation effects , Up-Regulation , Vitamin A/pharmacology , Vitamin A/therapeutic use , X-Rays
8.
J Vis Exp ; (169)2021 03 12.
Article in English | MEDLINE | ID: mdl-33779612

ABSTRACT

The control of such human diseases as dengue, Zika, and chikungunya relies on the control of their vector, the Aedes aegypti mosquito, because there is no prevention. Control of mosquito vectors can rely on chemicals applied to the immature and adult stages, which can contribute to the mortality of non-targets and more importantly, lead to insecticide resistance in the vector. The sterile insect technique (SIT) is a method of controlling populations of pests through the release of sterilized adult males that mate with wild females to produce non-viable offspring. This paper describes the process of producing sterile males for use in an operational SIT program for the control of Aedes aegypti mosquitoes. Outlined here are the steps used in the program including rearing and maintaining a colony, separating male and female pupae, irradiating and marking adult males, and shipping Aedes aegypti males to the release site. Also discussed are procedural caveats, program limitations, and future objectives.


Subject(s)
Aedes/physiology , Fertility/radiation effects , Insecticide Resistance , Mosquito Control/methods , Mosquito Vectors/physiology , Pupa/physiology , Sterilization, Reproductive/methods , Aedes/radiation effects , Animals , Female , Humans , Male , Mosquito Vectors/radiation effects , Pupa/radiation effects
9.
Reprod Toxicol ; 100: 90-100, 2021 03.
Article in English | MEDLINE | ID: mdl-33497741

ABSTRACT

Radiofrequency exposure from man-made sources has increased drastically with the era of advanced technology. People could not escape from such RF radiations as they have become the essential part of our routine life such as Wi-Fi, microwave ovens, TV, mobile phones, etc. Although non-ionizing radiations are less damaging than ionizing radiations but its long term exposure effect cannot be avoided. For fertility to be affected, either there is an alteration in germ cell, or its nourishing environment, and RF affects both the parameters subsequently, leading to infertility. This review with the help of in vitro and in vivo studies shows that RF could change the morphology and physiology of germ cells with affected spermatogenesis, motility and reduced concentration of male gametes. RF also results in genetic and hormonal changes. In addition, the contribution of oxidative stress and protein kinase complex after RFR exposure is also summarized which could also be the possible mechanism for reduction in sperm parameters. Further, some preventative measures are described which could help in reverting the radiofrequency effects on germ cells.


Subject(s)
Fertility/radiation effects , Infertility, Male/etiology , Radio Waves/adverse effects , Animals , DNA/radiation effects , Humans , Male , Mice , Oxidative Stress , Rats , Sperm Motility/radiation effects , Spermatogenesis/radiation effects , Spermatozoa/chemistry , Spermatozoa/radiation effects , Spermatozoa/ultrastructure , Testosterone/blood
10.
Electromagn Biol Med ; 40(1): 92-102, 2021 Jan 02.
Article in English | MEDLINE | ID: mdl-33471575

ABSTRACT

Recently, a decreasing rate of fertility has to be credited to an array of factors such as environmental, health and lifestyle. Male infertility is likely to be affected by the strong exposure to heat and radiations. The most common sources of nonionizing radiations are cell phones, laptops, Wi-Fi and microwave ovens, which may participate to the cause of male infertility. One of the major sources of daily exposure to non-ionizing radiation is mobile phones. A mobile phone is now basically dominating our daily life through better services such as connectivity, smartphone devices. However, the health consequences are linked with their usage are frequently ignored. Constant exposure to non-ionizing radiations produced from a cell phone is one of the possible reasons for growing male infertility. Recently, several studies have shown that cell phone users have altered sperm parameters causing declining reproductive health. Cell phone radiation harms male fertility by affecting the different parameters like sperm motility, sperm count, sperm morphology, semen concentration, morphometric abnormalities, increased oxidative stress along with some hormonal changes. This review is focusing on the prevailing literature from in vitro and in vivo studies suggesting that non-ionizing exposure negatively affects human male infertility.


Subject(s)
Radiation Exposure/adverse effects , Reproductive Health , Animals , Fertility/radiation effects , Humans , Radio Waves/adverse effects
11.
Int J Radiat Oncol Biol Phys ; 109(1): 84-94, 2021 01 01.
Article in English | MEDLINE | ID: mdl-32758642

ABSTRACT

PURPOSE: Photon radiation therapy (x-ray radiation therapy [XRT] and gamma-ray radiation therapy [GRT]) of tumors close to ovaries causes reproductive and endocrine sequelae due to ovarian primordial follicle depletion. Given its finite range, proton radiation therapy (PRT) can preserve ovarian function when ovaries are positioned distal to the spread-out Bragg peak (SOBP) in tumors of the abdominopelvic region. This study compared anti-Müllerian hormone (AMH) levels (a biomarker of ovarian function) and primordial follicle survival after in vivo mouse pelvic GRT versus PRT. METHODS AND MATERIALS: One hundred twenty-four female prepubertal mice received sham, GRT, or PRT with ovaries positioned at various depth with respect to the proton SOBP, with single doses of 1.8 or 0.2 Gy. AMH was measured at baseline, 1, 3, and 8 weeks after treatment, and the total number of surviving primordial follicles was counted. Multivariable linear mixed-effects modeling was used to assess the relationship between radiation therapy modality and dose on AMH and primordial follicle survival. RESULTS: For ovaries beyond the SOBP, ovarian function (P = .5) and ovarian primordial follicle (OPF; P = 1.0) were spared relative to sham controls. For ovaries in the SOBP plateau, ovarian function and primordial follicle reserve 8 weeks after treatment were reduced for all groups: 1.8 Gy GRT (ßAMH = -4.9 ng/mL; ßOPF = -728.2/animal), 1.8 Gy (relative biological effectiveness [RBE] = 1.1) PRT (ßAMH = -5.1 ng/mL; ßOPF = -728.2/animal), 0.2 Gy GRT (ßAMH = -2.5 ng/mL; ßOPF = -595.1/animal), and 0.2 Gy (RBE = 1.1) PRT (ßAMH = -3.0 ng/mL; ßOPF = -555.4/animal) relative to sham controls (all differences P < .001). CONCLUSIONS: This study uses an animal model to demonstrate the safety of proton therapy in sparing fertility. Ovaries positioned beyond the SOBP during PRT maintain ovarian reserve, suggesting that a proton beam has no energy and exit dose beyond SOBP. This study proposes that proton therapy is much safer than photon radiation therapy to protect ovarian follicles with the same dose, and it supports further testing of proton therapy for abdominopelvic tumors in young women.


Subject(s)
Fertility/radiation effects , Ovary/physiology , Ovary/radiation effects , Proton Therapy/adverse effects , Translational Research, Biomedical , Animals , Cell Survival/radiation effects , Dose-Response Relationship, Radiation , Female , Mice , Organs at Risk/radiation effects , Relative Biological Effectiveness
12.
Thyroid ; 31(4): 658-668, 2021 04.
Article in English | MEDLINE | ID: mdl-33012254

ABSTRACT

Introduction: Thyroid cancer is one of the most common carcinomas diagnosed in adolescents and young adults, with a rapidly rising incidence for the past three decades. Surgery is the standard treatment for patients with differentiated thyroid carcinoma (DTC), and when indicated, followed by radioactive iodine (RAI) treatment. The aim of this study was to evaluate the possible effects of RAI therapy on ovarian function and fertility in women. Methods: The PubMed, Embase, and Web of Science databases were systematically searched up to January 2020. In addition, a meta-analyses were performed for anti-Mullerian hormone (AMH) levels after RAI, comparison of AMH levels prior and 1 year after RAI, and pregnancy rates in patient with thyroid cancer receiving RAI compared with patients with thyroid cancer who did not receive RAI. Results: A total of 36 studies were eligible for full-text screening and 22 studies were included. The majority of the studies had a retrospective design. Menstrual irregularities were present in the first year after RAI in 12% and up to 31% of the patients. Approximately 8-16% of the patients experienced amenorrhea in the first year after RAI. Women who received RAI treatment (median dose 3700 MBq [range 1110-40,700 MBq]); had menopause at a slightly younger age compared with women who did not receive RAI treatment, 49.5 and 51 years, respectively (p < 0.001). Pooled AMH of the seven studies reporting AMH concentrations after RAI was 1.79 ng/mL. Of these, four studies reported AMH concentrations prior and 1 year after RAI. The mean difference was 1.50 ng/mL, which was significant. Finally, meta-analysis showed that patients undergoing RAI were not at a decreased risk of becoming pregnant. Conclusions: Most of the studies indicate that RAI therapy for DTC is not associated with a long-term decrease in pregnancy rates although meta-analyses show a significant decrease in AMH levels after RAI therapy. Prospective studies are needed to confirm these results. We recommend counseling patients about the possible effects of 131I and incorporate today's knowledge in multidisciplinary counseling.


Subject(s)
Fertility/radiation effects , Infertility, Female/etiology , Iodine Radioisotopes/adverse effects , Ovary/radiation effects , Radiation Injuries/etiology , Radiopharmaceuticals/adverse effects , Thyroid Neoplasms/radiotherapy , Adolescent , Adult , Cancer Survivors , Child , Female , Humans , Infertility, Female/diagnosis , Infertility, Female/physiopathology , Middle Aged , Ovary/physiopathology , Pregnancy , Pregnancy Rate , Radiation Injuries/diagnosis , Radiation Injuries/physiopathology , Risk Assessment , Risk Factors , Thyroid Neoplasms/pathology , Time Factors , Young Adult
13.
Breast Cancer ; 27(6): 1177-1186, 2020 Nov.
Article in English | MEDLINE | ID: mdl-32583350

ABSTRACT

BACKGROUND: The threat to fertility due to anticancer treatments can be distressing to women who wish to complete their family. The current study assessed the fertility-related concerns, psychological distress and health-related quality of life (HRQoL) of breast cancer survivors in comparison to non-cancer women with infertility history and to healthy controls from the general population. METHODS: We surveyed young adult women aged 18 to 40 who wished to have a (or another) biological child. Participants completed self-report measures assessing fertility concerns, anxiety, depression and physical, emotional, role and social functioning. Group differences were assessed using multivariate comparisons as well as univariate tests and discriminant analysis for individual measures. RESULTS: A total of 136 women were recruited, of whom 43 were breast cancer survivors, 56 non-cancer infertile women and 37 healthy controls. Considering the female cancer survivors as the focus of the analysis, data suggested that these women presented identical concerns to the non-cancer infertile group and higher than the healthy women with regard to fertility potential (p < 0.01). However, women diagnosed with cancer reported worse HRQoL than their counterparts, showing lower scores in physical functioning (p < 0.05) than infertile women and lower role (p < 0.05) and social HRQoL (p < 0.01) than the controls. Anxiety and depressive symptoms did not differ between the three groups. CONCLUSIONS: The results suggest that living with uncertainty about reproductive potential after cancer can be a disruptive experience. Breast cancer survivors and infertile women are at risk of future emotional maladjustments, given the reported level of fertility concern.


Subject(s)
Breast Neoplasms/therapy , Cancer Survivors/psychology , Infertility, Female/psychology , Stress, Psychological/epidemiology , Survivorship , Adult , Antineoplastic Agents/adverse effects , Anxiety/diagnosis , Anxiety/epidemiology , Anxiety/etiology , Anxiety/psychology , Cancer Survivors/statistics & numerical data , Chemoradiotherapy, Adjuvant/adverse effects , Cross-Sectional Studies , Depression/diagnosis , Depression/epidemiology , Depression/etiology , Depression/psychology , Female , Fertility/drug effects , Fertility/radiation effects , Fertility Preservation/methods , Fertility Preservation/psychology , Humans , Infertility, Female/etiology , Mastectomy , Neoadjuvant Therapy/adverse effects , Quality of Life , Self Report/statistics & numerical data , Social Interaction , Stress, Psychological/diagnosis , Stress, Psychological/etiology , Stress, Psychological/psychology , Uncertainty
14.
Thyroid ; 30(8): 1169-1176, 2020 08.
Article in English | MEDLINE | ID: mdl-32079487

ABSTRACT

Background: Differentiated thyroid carcinoma (DTC) during childhood is a rare disease. Its excellent survival rate requires a focus on possible long-term adverse effects. This study aimed to evaluate fertility in female survivors of childhood DTC by assessing various reproductive characteristics combined with anti-Müllerian hormone (AMH) levels (a marker of ovarian reserve). Methods: Female survivors of childhood DTC, diagnosed at ≤18 years of age between 1970 and 2013, were included. Survivors were excluded when follow-up time was less than five years or if they developed other malignancies before or after diagnosis of DTC. Survivors filled out a questionnaire regarding reproductive characteristics (e.g., age at menarche and menopause, pregnancies, pregnancy outcomes, need for assisted reproductive therapy). Survivors aged <18 years during evaluation received an altered questionnaire without questions regarding pregnancy and pregnancy outcomes. These data were combined with information from medical records. AMH levels were measured in serum samples and were compared with AMH levels from 420 women not treated for cancer. Results: Fifty-six survivors with a median age of 31.0 (interquartile range, IQR, 25.1-39.6) years were evaluated after a median follow-up of 15.4 (IQR 8.3-24.7) years. The median cumulative dose of 131I administered was 7.4 (IQR 3.7-13.0) GBq/200.0 (IQR 100.0-350.0) mCi. Twenty-five of the 55 survivors aged 18 years or older during evaluation reported 64 pregnancies, 45 of which resulted in live birth. Of these 55, 10.9% visited a fertility clinic. None of the survivors reported premature menopause. Age at AMH evaluation did not differ between DTC survivors and the comparison group (p = 0.268). Median AMH levels did not differ between DTC survivors and the comparison group [2.0 (IQR 1.0-3.7) µg/L vs. 1.6 (IQR 0.6-3.1) µg/L, respectively, p = 0.244]. The cumulative dose of 131I was not associated with AMH levels in DTC survivors (rs = 0.210, p = 0.130). Conclusions: Female survivors of DTC who received 131I treatment during childhood do not appear to have major abnormalities in reproductive characteristics nor in predictors of ovarian failure.


Subject(s)
Fertility/radiation effects , Infertility, Female/etiology , Iodine Radioisotopes/pharmacology , Thyroid Neoplasms/radiotherapy , Adult , Anti-Mullerian Hormone/blood , Child , Female , Follow-Up Studies , Humans , Netherlands , Ovarian Reserve/radiation effects , Pregnancy , Pregnancy Outcome , Surveys and Questionnaires , Survivors , Treatment Outcome
15.
Poult Sci ; 99(2): 812-819, 2020 Feb.
Article in English | MEDLINE | ID: mdl-32029163

ABSTRACT

The objective of this study was to determine the effect of age at photostimulation on sexual maturity and performance of layer breeders. A total of 192 fourteen-wk-old White Leghorn (WL) breeder hens were randomly allocated to 4 treatments of 48 birds each, with 2 replicates per treatment. The birds were photostimulated at 16 (PS16), 18 (PS18), 20 (PS20), and 22 (PS22) wk of age. Four birds per treatment were randomly selected to evaluate sexual organ development at 1 D before photostimulation and 2, 4, and 6 wk after photostimulation. The ovary weight, large yellow follicles number (LYF), oviduct weight, and oviduct length of PS18 increased sharply after photostimulation. Conversely, the increase in PS16 was not observed until 2 wk after photostimulation. There was no difference in age at sexual maturity between treatments (P > 0.05). The PS16 had the longest interval (28 D) from photostimulation to 5% egg production, while PS22 reached 5% egg production 7 D before photostimulation. The PS22 had lower peak production (P = 0.02) and less egg production (P = 0.02) than other treatments. The PS16 had more broken and abnormal eggs (P = 0.01) and lower hatchability (P = 0.04) than other treatments. In conclusion, photostimulation at 16 and 22 wk of age decreases hatchability and egg production, respectively, and photostimulation at 18 wk is appreciated for the WL breeder hens.


Subject(s)
Chickens/physiology , Egg Shell/radiation effects , Fertility/radiation effects , Photic Stimulation , Reproduction/radiation effects , Sexual Maturation/radiation effects , Age Factors , Animals , Egg Shell/physiology , Female , Random Allocation
16.
Int J Mol Sci ; 21(4)2020 Feb 20.
Article in English | MEDLINE | ID: mdl-32093393

ABSTRACT

Over the last decade, the number of cancer survivors has increased thanks to progress in diagnosis and treatment. Cancer treatments are often accompanied by adverse side effects depending on the age of the patient, the type of cancer, the treatment regimen, and the doses. The testicular tissue is very sensitive to chemotherapy and radiotherapy. This review will summarize the epidemiological and experimental data concerning the consequences of exposure to chemotherapy during the prepubertal period or adulthood on spermatogenic progression, sperm production, sperm nuclear quality, and the health of the offspring. Studies concerning the gonadotoxicity of anticancer drugs in adult survivors of childhood cancer are still limited compared with those concerning the effects of chemotherapy exposure during adulthood. In humans, it is difficult to evaluate exactly the toxicity of chemotherapeutic agents because cancer treatments often combine chemotherapy and radiotherapy. Thus, it is important to undertake experimental studies in animal models in order to define the mechanism involved in the drug gonadotoxicity and to assess the effects of their administration alone or in combination on immature and mature testis. These data will help to better inform cancer patients after recovery about the risks of chemotherapy for their future fertility and to propose fertility preservation options.


Subject(s)
Antineoplastic Agents/adverse effects , Chemoradiotherapy/adverse effects , Fertility Preservation , Fertility , Neoplasms/therapy , Spermatogenesis , Adult , Antineoplastic Agents/therapeutic use , Child , Fertility/drug effects , Fertility/radiation effects , Humans , Male , Spermatogenesis/drug effects , Spermatogenesis/radiation effects
17.
J Pediatr Hematol Oncol ; 42(8): e807-e809, 2020 11.
Article in English | MEDLINE | ID: mdl-31415018

ABSTRACT

Survivors of childhood cancer are at risk of long-term sequelae that arise as a consequence of cancer treatment. Radiation and chemotherapy treatment in pediatric female patients can have detrimental impacts on fertility, particularly in those with pelvic tumor involvement. We report 2 successful natural full-term pregnancies with vaginal delivery in a woman 12 years after biopsy, irradiation (55.5 Gy), and multi-agent chemotherapy for treatment of pelvic Ewing sarcoma. Both children were born healthy, with no complications in pregnancy or delivery. Fertility preservation and risk assessment following chemotherapy/radiation therapy is evolving, providing new data to effectively counsel and treat young women.


Subject(s)
Bone Neoplasms/therapy , Chemoradiotherapy/methods , Fertility Preservation/methods , Fertility/physiology , Pelvic Neoplasms/therapy , Sarcoma, Ewing/therapy , Adult , Bone Neoplasms/pathology , Cancer Survivors , Female , Fertility/drug effects , Fertility/radiation effects , Humans , Pelvic Neoplasms/pathology , Pregnancy , Pregnancy Outcome , Radiotherapy Dosage , Sarcoma, Ewing/pathology
18.
Int J Cancer ; 146(3): 829-838, 2020 02 01.
Article in English | MEDLINE | ID: mdl-30989639

ABSTRACT

Advances in multimodality cancer treatments have increased the risk of long-term complications in early-onset cancer survivors. For female cancer survivors, these include diminished reproductive function, often resulting in a narrowed fertile window. The aim of our study was to evaluate the use of fertility treatments in cancer survivors (aged 0-39 years at diagnosis) compared to siblings. Data from Finnish registers on cancer, birth and prescribed medications were merged to identify 8,929 survivors and 9,495 siblings without previous deliveries. Fertility drug purchases from 1993 to 2012 at the age of 16-41 years were included. A Poisson regression model was used to estimate incidence rate ratios (IRRs) for the use of fertility drugs, adjusting for age and calendar time at fertility drug purchase. Fertility treatments were more common in survivors compared to siblings, as 6.1% of survivors compared to 3.8% of siblings had bought fertility drugs (IRR 1.43, 95% confidence interval [CI] 1.25-1.65). A subclassification of fertility treatments into ovulation inductions and assisted reproductive technology (ART), showed increased use of ART (IRR 2.41, 95% CI 1.97-2.96), whereas the use of ovulation induction was similar in survivors and siblings. Analyses by calendar time periods showed the use of ART to be significantly higher in the most recent decade, from 2003 onwards. We conclude that cancer survivors have an increased risk for subfertility, which is why fertility counseling is important. However, our results mirror a more active approach among clinicians towards fertility treatments in cancer survivors during the most recent years.


Subject(s)
Cancer Survivors/statistics & numerical data , Fertility Agents/therapeutic use , Infertility, Female/therapy , Neoplasms/complications , Adolescent , Adult , Antineoplastic Agents/adverse effects , Case-Control Studies , Child , Child, Preschool , Drug Prescriptions/statistics & numerical data , Female , Fertility/drug effects , Fertility/radiation effects , Finland , Humans , Infant , Infant, Newborn , Infertility, Female/etiology , Male , Neoplasms/mortality , Neoplasms/therapy , Pregnancy , Radiotherapy/adverse effects , Registries/statistics & numerical data , Reproductive Techniques, Assisted/statistics & numerical data , Siblings , Young Adult
19.
Hum Reprod Update ; 26(2): 161-173, 2020 02 28.
Article in English | MEDLINE | ID: mdl-31863097

ABSTRACT

BACKGROUND: As cancer survival rates improve, understanding and preventing the adverse off-target and long-term impacts of cancer treatments, including impacts on fertility, have become increasingly important. Cancer therapy-mediated damage to the ovary and depletion of the primordial follicle reserve are well characterised. However, our knowledge of the full extent of damage to the rest of the female reproductive tract, in particular the uterus, is limited. OBJECTIVE AND RATIONALE: Improving our understanding of the off-target effects of cancer therapies on the entire female reproductive tract is a critical step towards developing truly effective strategies to protect the fertility of cancer survivors. The objective of this narrative review was to critically evaluate the available literature regarding the capacity for the uterus to sustain a healthy pregnancy following exposure to radiotherapy or chemotherapy. SEARCH METHODS: The authors performed PubMed (Medline) searches using the following key words: uterus, cancer survivors, radiotherapy, chemotherapy, pregnancy outcome, fertility preservation, infertility. There were no limits placed on time of publication. OUTCOMES: Overall, there were major limitations to the current available literature, meaning that interpretations should be taken with caution. Despite these drawbacks, data suggest that the uterus may sustain off-target damage, with the extent of damage dependent on the type of cancer treatment and patient age. Specifically, uterine growth is stunted and resistant to hormone replacement therapy in prepubertal girls receiving abdominal, pelvic or whole-body radiotherapy. In contrast, females treated with radiotherapy post-puberty can benefit from hormone replacement therapy, as demonstrated by increased uterine volume and function. No live births have been reported in women previously exposed to radiotherapy after transplantation of cryopreserved ovarian tissue, even when menstruation returns. However, this technique has proven to be a successful fertility preservation method for women previously treated with chemotherapy. Obstetricians commonly report that women who maintain sufficient ovarian function can achieve pregnancy naturally following radiotherapy, but they have thin and/or fibrotic myometrium at delivery, compromising safe delivery and subsequent pregnancy. Furthermore, women exposed to either radiotherapy or chemotherapy have a higher prevalence of preterm birth and low birth weight infants, even in those with normal ovarian function or when oocyte donation is utilised. The mechanisms of potential uterine damage are poorly understood. While the myometrium, vasculature and endometrial progenitor cells are possibly targets, further studies are clearly required and well-controlled animal models could provide the best avenue for these types of future investigations. WIDER IMPLICATIONS: Female cancer survivors experience greater rates of early pregnancy loss and complications, suggesting that cancer therapy-induced damage to the uterus contributes to infertility. Despite clinical reports dating back to 1989, we highlight a surprising lack of detail in the literature regarding the precise nature and extent of off-target damage inflicted to the uterus in response to cancer therapies. Young women requiring cancer treatment, and the clinicians treating them, must be equipped with accurate information to aid informed decision-making regarding cancer treatment regimens as well as the development and use of effective fertility preservation measures. As the current literature on the impacts of cancer treatments is limited, we hope that our narrative review on this subject will stimulate more research in this important field.


Subject(s)
Antineoplastic Protocols , Fertility/physiology , Neoplasms/therapy , Pregnancy Outcome , Uterine Diseases , Uterus/pathology , Animals , Drug-Related Side Effects and Adverse Reactions/epidemiology , Drug-Related Side Effects and Adverse Reactions/pathology , Drug-Related Side Effects and Adverse Reactions/physiopathology , Female , Fertility/drug effects , Fertility/radiation effects , Fertility Preservation/methods , Humans , Infant, Newborn , Neoplasms/pathology , Neoplasms/physiopathology , Ovary/drug effects , Ovary/physiology , Ovary/radiation effects , Pregnancy , Pregnancy Outcome/epidemiology , Radiation Injuries/epidemiology , Radiation Injuries/pathology , Radiation Injuries/physiopathology , Radiotherapy/adverse effects , Uterine Diseases/epidemiology , Uterine Diseases/etiology , Uterine Diseases/physiopathology , Uterus/drug effects , Uterus/radiation effects
20.
Fertil Steril ; 112(6): 1022-1033, 2019 12.
Article in English | MEDLINE | ID: mdl-31843073

ABSTRACT

Patients preparing to undergo gonadotoxic medical therapy, radiation therapy, or gonadectomy should be provided with prompt counseling regarding available options for fertility preservation for iatrogenic infertility. Fertility preservation can best be provided by comprehensive programs designed and equipped to confront the unique challenges facing these patients. This document replaces the document with a similar name, last published in 2013.


Subject(s)
Antineoplastic Agents/adverse effects , Castration/adverse effects , Fertility Preservation , Iatrogenic Disease , Infertility, Female/therapy , Infertility, Male/therapy , Radiation Injuries/therapy , Reproductive Techniques, Assisted , Female , Fertility/drug effects , Fertility/radiation effects , Fertility Preservation/adverse effects , Humans , Infertility, Female/etiology , Infertility, Female/physiopathology , Infertility, Male/etiology , Infertility, Male/physiopathology , Male , Radiation Injuries/etiology , Radiation Injuries/physiopathology , Radiotherapy/adverse effects , Reproductive Techniques, Assisted/adverse effects , Risk Factors , Treatment Outcome
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