Menstrual Dysfunction in Female Patients Undergoing Dialysis Resic H 1, Alajbegovic A 2, Sahovic V 1, Mesic E 3, Suljic E 2

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BANTAO Journal 2 (2): p 22; 2004 Menstrual Dysfunction in Female Patients Undergoing Dialysis Resic H 1, Alajbegovic A 2, Sahovic V 1, Mesic E 3, Suljic E 2 1 Center for Haemodialysis, University Clinical Center, Sarajevo, 2 Neurology Clinic University Clinical Center, Sarajevo, 3 Clinic for Nephrology, Dialysis and Kidney Transplantation, University of Tuzla Abstract Uremia is associated with different endocrinologic abnormalities, which in some cases induce polyendocrinopathia. Female patients on dialysis are often subject to menstrual disorders that are variously manifested. We evaluated the etiology of menstrual dysfunctions in female dialysis patients. History, clinical and hormonal tests were performed on 25 female patients that were in chronic dialysis program 4 hours, 3 times per week. Oligomenorrhea was considered as menstrual interval between 35 and 90 days and amenorrhea as cease of menstruation in the last six months. All patients had had normal menstrual cycle before the dialysis. Mean age of patients was 42,79,96 years and mean dialysis duration was 75,562,41 months. Out of 25 patients, 10 had developed amenorrhea when beginning dialysis and 5 of them regained regular menstrual cycle after one year. 7 patients had oligomenorrhea and 8 patients had an early menopause. Prolactin concentration was significantly higher in group which developed menopause (N=8), cpr=1222,31013,4, amenorrhea (942,21061,2), oligomenorrhea (860,4897,2), compared to the group with regular menstruation cycle (444,8299,7). LH level in serum was increased in all groups. FSH was insignificantly higher in groups with oligomenorrhea and amenorrhea and amounted to 51,169,9, while β-estradiol and progesterone were in normal ranges. Haemodialysis duration influenced the prolactin level and after one year of follow up prolactin level significantly decreased in the group with amenorrhea that regained regular menstruation (cpr=596,2297,2). Conclusion: Different menstrual disorders develop in dialyzed patients. Hyperprolactinemia was present in our dialysis population. Significant lowering of prolactin level in 20 % of patients led to normalization of menstrual cycle. Introduction Uremia is associated with different endocrinologic abnormalities which, in some cases, induce multiple endocrinopathy. Symptoms of sexual function abnormalities in dialysis patients are decrease in libido, reduced frequency of sexual intercourses, galactorrhea, menstrual abnormalities, no ovular cycles, amenorrhea and infertility. The aim of our study is to evaluate the etiology of menstrual dysfunction in female patients undergoing dialysis. Material and methods Female patients on dialysis are often subject to menstrual disorders which are variously manifested. History, clinical and hormonal tests were performed on 25 female patients that underwent chronic dialysis program 4 hours 3 times per week. None of the patients was diabetic. Patients were allocated to different groups according to their menstrual status at the time of investigation as follows: a) patients with oligomenorrhea (menstrual interval between 35-90 days); b) patients with amenorrhea (as cause of menstruation in the last six months); c) patients with regular ovular cycles; d) patients with early menopause. Full informed consent was obtained from each patient. Patients menstrual histories of the subjects before and during the CHD therapy were investigated. Hormonal status entailed determining the serum levels of the luteinizing hormone (LH), the folliclestimulating hormone (FSH), prolactin (PRL), estradiol and progesterone in one-year follow-up period. Before blood sampling, we confirmed that the patient had not received any hormone preparation during the previous three months. Levels of hormones were assayed using RIA kits. Inter-group comparisons were made by an unpaired Student s t-test. Results All patients had normal menstrual cycle before the dialysis. Immediately after the beginning of CHD therapy 10 females developed amenorrhea, 7 oligomenorrhea and 8 patients developed menopause. 5 of amenorrhoeic women returned to regular cycles. Table 1 presents average age of females undergoing haemodialysis, while average haemodialysis duration was 75.562.41 months. Table 3 summarizes the baseline characteristics of the hormonal data. The serum FSH and LH were significantly increased during a follow up period, the serum level of PRG was higher, but not significantly. Serum levels were lover in patients with menstrual disorders, as progesterone. Correspondence to: Halima Resic, Center for Haemodialysis, University Clinical Center, Sarajevo

BANTAO Journal 2 (2): p 23; 2004 Before CHD regular cycles N = 25 After CHD amenorrhea N =10 oligomenorrhea (N = 7) regular cycles (N = 5) amenorrhea/menopausa (N = 5) (N = 8) Fig. 1 Menstrual histories of the female patients undergoing dialysis. Table 1. Avarage age of females undergoing haemodialysis Diagnosis Number of patients Age (years) Standard error Total 25 46.7 9.96 2.03 Amenorrhea 5 47.0 3.28 1.47 Oligomenorrhea 7 49.2 4.18 1.71 5 47.2 3.71 1.51 Menopause 8 49.8 5.29 187 Table 3. Hormone status in patients undergoing haemodialysis Hormones First Second Fnding T-test FSH 74.0 81.3 96.780.3 22.750.3 p<0.05 LH 66.5 72.0 94.169.2 27.656.4 p<0.05 Estradiol 407.8472.1 442.3555.3 34.5387.6 n.s. Progesteron 6.046.14 6.225.79 0.186.82 n.s. Prolactin 959.5889.7 740.3564.1 219.2695. 4 n.s.

BANTAO Journal 2 (2): p 24; 2004 Table 4a. Avarage hormone s (FSH) Amenorrhea 51.1 69.9 Oligomenorrhea 55.5 74.8 98.5 84.4 Menopause 98.9 71.7 108.9 71.5 87.45 80.3 75.4 88.1 111.2 75.8 57.8 52.5 p < 0.07 31.9 57.3-9.0 18.1 12.3 35.3 Table 4a summarizes characteristics of the FSH level in different groups during a follow up period; FSH was significantly higher in groups with oligomenorrhea and amenorrhea. Serum LH levels were markedly elevated in all groups (Table 4b). Serum estradiol levels were lower in patients with menstrual disorders (Table 4c). Table 4e summarizes characteristics of the serum prolactin level which remained low. Table 4b. Avarage hormone s (LH) Amenorrhea 48.2 64.7 Oligomenorrhea 59.7 80.8 82.2 72.0 Menopause 79.6 58.3 97.5 53.6 99.4 88.5 73.9 81.1 100.6 47.3 49.3 63.5 39.7 72.0 1.9 4.4 21.0 47.8 Table 4c. Avarage hormone s (estradiol) Amenorrhea 493.4 276.4 Oligomenorrhea 553.5 781.0 299.7 444.8 Menopause 222.0 198.5 163.4 65.2 537.5 686.2 611.0 578.7 439.7 535.5-330.1 245.4-160.0 328.7 166.2 363.2 217.7 346.8 p< 0.05

BANTAO Journal 2 (2): p 25; 2004 Table 4d. Average hormone levels (progesterone) Amenorrhea 3.42 1.09 Oligomenorrhea 3.20 1.45 9.68 11.62 Menopause 6.37 4.48 2.74 1.50 4.65 2.42 11.86 9.49 6.03 2.38-0.68 1.74 1.45 1.43 0.24 13.4-0.34 4.31 p<0.05 Table 4e. Average hormone levels (prolactin) Diagnosis First Amenorrhea 860.4 796.9 Oligomenorrhea 942.2 1061.0 711.6 225.2 Menopause 1222.3 013.4 897.2 887.2 596.2 297.2 530.0 122.3 902.1 551.2 36.8 97.6 346.0 1176.0-181.6 203.1-320.2 543.1 p<0.001 p<0.001 Discussion The main causes of endocrine dysfunctions in uremia are intoxication not adequately corrected by current treatments, nutritional deficiencies, electrolyte abnormalities and mineral metabolism acidosis. In this study all patients with regular menstruation before dialysis developed amenorrhea once dialysis started. In our study amenorrhea persisted in five women, while five returned to regular cycles. Three out of 5 women with regular cycles had anovulatory menstruation what suggests that dialysis had long-term effects on ovaries function. Primson et al examined the metabolic processing of the luteinizing hormone releasing hormone (LH RH) and they noted reduced MCR and prolonged half-life in patients with renal failure. Therefore, abnormalities in gonadotropin (LH and FSH) secretion arise in patients undergoing dialysis inducing ovarian dysfunction (3). The influence of dialysis on the MCR of LH RH may result in a continuous increase of the LH level (2). The serum FSH levels were neither elevated nor lowered. Endocrinologic s of gonodotropins in patients undergoing dialysis are consistent with those reported by several investigators (4,5). The prolactin level (PRL) in our group with amenorrhea, oligomenorrhea and menopause was significantly higher than the one in group with regular menstrual cycle. Many investigators have reported that hyperprolactinemia contributes to ovarial dysfunction in women undergoing CHD (5,6). Therefore, hyperprolactinemia might be an important cause of ovarial dysfunction. Menstruation recovered in 5 out of 10 patients who developed amenorrhea during dialysis. This can be explained by the erythropoietin effect which was administered to women with regular menstrual cycles. Conclusion Patients undergoing dialysis developed different menstrual disorders. Specific endocrine differences between the group with regular menstrual cycle and the group with menstrual disorders were present in the prolactin level. Significant lowering of the prolactin level in 20% of patients led to normalization of menstrual cycle. Long term dialysis might improve menstrual disorders in such patients.

BANTAO Journal 2 (2): p 26; 2004 References: 1. Angela Rosa Pinearoli. Hormonal changes in daily haemodialysis. Seminars in Dialysis, vol. 12, no. 6, 1999, p 455-461. 2. Sirenstsen GD, Lim SD, Nakawatose C, Frotam LA, Metabolic clearance and sechetion notes of human prolactin in normal subjects and in patients with chronic renal failure. I. Clin. Endocrinol Melb 1997; 44: 356-360 3. Swamy AP, Woolf PD, Cesteno RV. Hypotalamic pitritory ovarium axis in uremic woman. Lab. Clin. Med 1979; 93: 1066-1072 4. Perez RI, Lipner H, Abdulla N, Cicero S, Abrams M. Menstrual dysfunction of patients undergoing chrome haemodialysis. Obstret gyneed 1978; 51: 522-555 5. Weizman R, Weizman A, Levi I, Gura V, Zevin D, Maoz B, Wijsenbeck H, Ben David M. Sexual dysfunction associated with hyperprolactinemia in males and females undergoing haemodialysis. Psychosom Med 1983; 45: 259-269 6. Rickko Kawashima, Tsutomi Doreti, Toshimichi Oki, Mitsuhiro Yoshinaga, Yukihiro Nagata. Menstrual disorders in patients undergoing chronic haemodialysis. I. Obstet Gynaeed. Res vol 24. No 5: 367-373, 1998