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      Fertility, sexuality and testicular adrenal rest tumors in adult males with congenital adrenal hyperplasia

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          Abstract

          Objective

          Fertility in males with congenital adrenal hyperplasia (CAH) is reported from normal to severely impaired. Therefore, we investigated fertility/fecundity, social/sexual situation, and pituitary–gonadal function in CAH males.

          Subjects and methods

          The patient cohort comprised 30 males, aged 19–67 years, with 21-hydroxylase deficiency. Their fertility was compared with age-matched national population data. For the evaluation of social/sexual factors and hormone status, age-matched controls were recruited ( n=32). Subgroups of different ages (<30 years and older) and CYP21A2 genotypes (null (severe salt-wasting (SW)), I2splice (milder SW), and I172N (simple virilizing)) were also studied. Patients underwent testicular ultrasound examination ( n=21) and semen analysis ( n=14).

          Results

          Fertility was impaired in CAH males compared with national data (0.9±1.3 vs 1.8±0.5 children/father, P<0.001). There were no major differences in social and sexual factors between patients and controls apart from more fecundity problems, particularly in the I172N group. The patients had lower testosterone/estradiol (E 2) ratio and inhibin B, and higher FSH. The semen samples were pathological in 43% (6/14) of patients and sperm concentration correlated with inhibin B and FSH. Testicular adrenal rest tumors (TARTs) were found in 86% (18/21). Functional testicular volume correlated positively with the testosterone/E 2 ratio, sperm concentration, and inhibin B. Patients with pathological semen had increased fat mass and indications of increased cardiometabolic risk.

          Conclusions

          Fertility/fecundity was impaired in CAH males. The frequent occurrence of TARTs resulting in testicular insufficiency appears to be the major cause, but other factors such as elevated fat mass may contribute to a low semen quality.

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          Most cited references28

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          Male obesity and alteration in sperm parameters.

          To study the effect of male obesity on sperm parameters and erectile dysfunction. Retrospective analysis. Referral fertility center. Couples presenting for infertility treatment. On presentation, all men reported their weight and height and filled out an intake form that includes questions regarding factors that affect male infertility, including presence of erectile dysfunction. Body mass index (BMI) was divided into three groups: normal (BMI or=30 kg/m(2)). Sperm parameters reviewed included sperm concentration and progressively motile sperm count. Oligozoospermia, low progressively motile sperm count, and self-reported erectile dysfunction. The mean age of the study population was 32.8 +/- 0.3 years. Among the 526 patients, 10.2% (54 of 526) were excluded because of the presence of a male factor known to affect fertility. The incidence of oligozoospermia increased with increasing BMI: normal weight = 5.32%, overweight = 9.52%, and obese = 15.62%. The prevalence of a low progressively motile sperm count was also greater with increasing BMI: normal weight = 4.52%, overweight = 8.93%, and obese = 13.28%. The incidence of erectile dysfunction did not vary across BMI categories when corrected for potential contributing factors. Male obesity is associated with increased incidence of low sperm concentration and low progressively motile sperm count.
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            Gender role behavior, sexuality, and psychosocial adaptation in women with congenital adrenal hyperplasia due to CYP21A2 deficiency.

            Gender-atypical behavior has been described in young girls as well as in women with congenital adrenal hyperplasia (CAH) due to a CYP21A2 deficiency. The aim of the study was to assess health-related, psychosexual, and psychosocial parameters and correlate the results to CYP21A2 genotype. Sixty-two Swedish women with CAH and age-matched controls completed a 120-item questionnaire and a validated quality of life instrument [psychological general well-being (PGWB) formula] to identify psychosexual and psychosocial parameters. The patients were divided into four CYP21A2 genotype groups. The women with CAH held more male-dominant occupations (30%) compared to controls (13%) (P = 0.04), especially those in the null genotype group (55%) (P = 0.006). They also reported a greater interest in rough sports (74%) compared to controls (50%) (P = 0.007). Eight women with CAH (14%) reported a prime interest in motor vehicles, compared to none of the controls (P = 0.002). Non-heterosexual orientation was reported by 19% of women with CAH (P = 0.005), 50% in the null genotype group (P = 0.0001), 30% in I2 splice (NS), and 5% in I172N (NS). PGWB total score did not differ between patients and controls. We identified increased gender-atypical behavior in women with CAH that could be correlated to the CYP21A2 genotype. This speaks in favor of dose-dependent effects of prenatal androgens on the development of higher brain functions. The impact of the disease on upbringing and interpersonal relationships did not correlate with disease severity, indicating that other factors, such as coping strategies, are important for psychosocial adaptation. This illustrates the need for psychological support to parents and patients.
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              Androgen and psychosexual development: core gender identity, sexual orientation and recalled childhood gender role behavior in women and men with congenital adrenal hyperplasia (CAH).

              We assessed core gender identity, sexual orientation, and recalled childhood gender role behavior in 16 women and 9 men with CAH and in 15 unaffected female and 10 unaffected male relatives, all between the ages of 18 and 44 years. Women with congenital adrenal hyperplasia (CAH) recalled significantly more male-typical play behavior as children than did unaffected women, whereas men with and without CAH did not differ. Women with CAH also reported significantly less satisfaction with the female sex of assignment and less heterosexual interest than did unaffected women. Again, men with CAH did not differ significantly from unaffected men in these respects. Our results for women with CAH are consistent with numerous prior reports indicating that girls with CAH show increased male-typical play behavior. They also support the hypotheses that these women show reduced heterosexual interest and reduced satisfaction with the female sex of assignment. Our results for males are consistent with most prior reports that boys with CAH do not show a general alteration in childhood play behavior. In addition, they provide initial evidence that core gender identity and sexual orientation are unaffected in men with CAH. Finally, among women with CAH, we found that recalled male-typical play in childhood correlated with reduced satisfaction with the female gender and reduced heterosexual interest in adulthood. Although prospective studies are needed, these results suggest that those girls with CAH who show the greatest alterations in childhood play behavior may be the most likely to develop a bisexual or homosexual orientation as adults and to be dissatisfied with the female sex of assignment.

                Author and article information

                Journal
                Eur J Endocrinol
                EJE
                European Journal of Endocrinology
                BioScientifica (Bristol )
                0804-4643
                1479-683X
                March 2012
                1 December 2011
                : 166
                : 3
                : 441-449
                Affiliations
                [1 ]simpleDepartment of Endocrinology, Metabolism and Diabetes, D02:04 simpleKarolinska Institute, Karolinska University Hospital SE-171 76, StockholmSweden
                [2 ]simpleDepartment of Molecular Medicine and Surgery simpleKarolinska Institute, Karolinska University Hospital SE-171 76, StockholmSweden
                [3 ]simpleDepartment of Andrology simpleKarolinska Institute, Karolinska University Hospital SE-171 76, StockholmSweden
                [4 ]simpleDepartment of Obstetrics and Gynecology simpleKarolinska Institute, Karolinska University Hospital SE-171 76, StockholmSweden
                [5 ]simpleDepartment of Endocrinology simpleSahlgrenska Academy, Sahlgrenska University Hospital, University of Gothenburg GöteborgSweden
                [6 ]simpleDepartment of Obstetrics and Gynecology simpleAkershus University Hospital LørenskogNorway
                [7 ]simpleKarolinska Institute, Centre for Inherited Metabolic Disorders (CMMS) simpleKarolinska University Hospital SE-171 76, StockholmSweden
                Author notes
                (Correspondence should be addressed to H Falhammar at Department of Endocrinology, Metabolism and Diabetes, D02:04, Karolinska Institute, Karolinska University Hospital; Email: henrik.falhammar@ 123456ki.se )
                Article
                EJE110828
                10.1530/EJE-11-0828
                3290120
                22157069
                b72c7293-d779-45d7-b0f4-8c3188230dea
                © 2012 European Society of Endocrinology

                This is an Open Access article distributed under the terms of the European Journal of Endocrinology's Re-use Licence which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 22 September 2011
                : 8 December 2011
                Funding
                Funded by: Swedish Research Council
                Award ID: 12198
                Categories
                Clinical Study

                Endocrinology & Diabetes
                Endocrinology & Diabetes

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