Materials and Methods: Thirty-six patients who applied to the pediatric endocrinology and urology outpatient clinics with the diagnosis of hypospadias were evaluated retrospectively. Risk factors were evaluated by recording the parental ages, exposure to environmental factors, the maternal BMI, history of pregnancy, drug use, and the father's fertility status.
Results: The mean age of the patients was 3.5 ± 2 years. The patients had anterior (n:27 : 75%), middle (midshaft) (n:8 ; 22.2%), and posterior (n:1 ; 2.8%) hypospadias. The mean body mass index (BMI) of the mothers was 24 ± 4.1 kg/m2. Eight (22.2%) mothers were overweight and six (16.6%) mothers were obese. There was a history of hypospadias in the family of 4 (11%) patients.
Conclusion: Although combinations of environmental and genetic factors play a role in the etiology of hypospadias, many unexplained factors are responsible for this disease.
Table 1: Risk factors for hypospadiasis associated with the patient and his parents
Assisted reproductive technologies are widely used for couples who apply to health institutions for infertility. Hormonal treatment is often applied during these methods. Many studies have shown that the use of assisted reproductive techniques increases the risk of hypospadias [8,17]. The risk is increased frequently after the intracytoplasmic sperm injection (ICSI) method [18,19]. In our study, assisted reproduction techniques with ICSI method were applied to the parents of 3 (8.3%) patients diagnosed with hypospadias.
It is known that some maternal factors are effective in the development of hypospadias. It has been shown that the presence of obesity in the mother is associated with hypospadias [20]. Endogenous levels of free estradiol increase with increasing BMI which may play a role in the development of hypospadias [21]. Many studies have shown that the risk of hypospadias increases in children of overweight or obese mothers [22,23]. However, Rankin et al. showed that obesity was not associated with hypospadias [24]. In our study, the mothers of 8 (22.2%) patients were overweight, and the mothers of 6 (16.6%) patients were obese.
It has been found that the risk of hypospadias is higher in children with low birth weight [12,15]. It is known that human chorionic gonadotropin (hCG) secreted from the placenta in the fetus stimulates fetal testicular steroidogenesis. Placental insufficiency may result in inadequate provision of fetal hCG and fetal nutrients, possibly explaining the association between hypospadias and low birth weight [25]. In addition, several studies have shown that preterm birth may be associated with late placental dysfunction and cause hypospadias [26,27]. In 2 (5.5%) of the patients in our study, history of low birth weight was elicited, and none of the mothers of the patients had a history of premature delivery.
Lower sperm count, sperm motility and higher abnormal sperm morphology were found in fathers of children with hypospadias [28]. It is stated in the testicular dysgenesis syndrome (TDS) hypothesis that hypospadias and male subfertility may share the same genetic and environmental factors [29]. In this way, subfertile fathers may transmit a certain predisposition to their children. Oligospermia was present in the fathers of our 3 (8.3%) patients.
When occupational exposures are evaluated, although there are conflicting results in terms of the relationship between exposure to pesticides and hypospadias, it has been shown that fathers exposed to pesticides are more likely to have children with hypospadias [30,31]. There was no occupational pesticide exposure in the parents of any of our patients.
Our study has some limitations. Since it is a retrospective study, we could not obtain data about some etiologic factors responsible for the development of hypospadias.
Ethics Committee Approval: Ethics committee approval was not obtained due to the retrospective nature of the study. Informed consent forms were obtained.
Informed Consent: An informed consent was obtained from the parents of all patients.
Publication: The results of the study were not published in full or in part in form of abstracts.
Peer-review: Externally peer-reviewed.
Authorship Contributions: Any contribution was not made by any individual not listed as an author. Concept – E.C.B., A.B., E.C.B.; Design – E.C.B., A.B., E.C.B.; Supervision – E.C.B., A.B., O.T.; Resources – E.C.B., A.B., E.C.B., O.T.; Materials – E.C.B., A.B., E.C.B., O.T.; Data Collection and/or Processing – E.C.B., A.B., E.C.B., O.T.; Analysis and/or Interpretation – E.C.B., A.B., E.C.B., O.T.; Literature Search – E.C.B., A.B., E.C.B., O.T.; Writing– E.C.B., A.B.; Critical Review – E.C.B., A.B., O.T.
Conflict of Interest: The authors declare that they have no conflict of interest.
Financial Disclosure: The authors declare that this study received no financial support.
4) Duckett JW. Hypospadias. Pediatr Rev 1989;11:37–42. https://doi.org/10.1542/pir.11-2-37.