{"title":"青春期少女原发性和继发性少经的临床和激素特征","authors":"S. Levenets, N. O. Udovikova, S. Novokhatska","doi":"10.30978/ujpe2019-2-28","DOIUrl":null,"url":null,"abstract":"The objective was to provide a comparative characteristic of clinical and hormonal parameters in secondary and primary oligomenorrhea (OM II and OM I) in adolescent girls. Materials and methods. A total of 185 girls with OM aged 13—17 years (142 with OM I and 43 with OM II) and 107 girls with a regular menstrual cycle (regMС — comparison group (CG)) were examined. We analyzed clinical and anamnestic indicators, data of ultrasound of the pelvic organs, LH, FSH, estradiol, and testosterone levels. Results and discussion. Family history of impaired function of the reproductive system in girls with OM II were less likely than with OM I (12.5 vs. 25.8 %; рφ < 0.002). Mothers of girls with OM gave birth more often at an early reproductive age than in CG (14.5 and 4.9 %; рφ < 0.001). Delayed menarche (15 years and later) with OM I was 5 times more frequent than in CG (24,1 vs 4,7 %; рφ< 0,001), while in OM II its frequency did not differ significantly from CG. Normal body mass index (BMI) in OM was less frequent than in women with reg MС (40.8 and 72.2 %, pφ < 0.001). In OM II, uterine hypoplasia was less common than in OM I (38.5 and 53.9 %; pφ < 0.05). Hypogonadotropinemia was more frequent with OM II than with OM I (21.6 versus 4.3 %; рφ < 0.001), and an increase in blood testosterone levels was more common with OM I than with OM II (24.1 versus 5.6 %; рφ < 0.01). Restoration of menstrual dysfunction was more frequent with OM II than with OM I (79.5 versus 63.4 %; рφ < 0.03). Conclusions . OM I is characterized by delayed menarche, hypoplasia of the uterus, family history of impaired function of the reproductive system and increased testosterone levels. OM II is associated with lack of stable normalization of menstrual function, marked hirsutism and hypogonadotropinemia.","PeriodicalId":243962,"journal":{"name":"Ukrainian Journal of Pediatric Endocrinology","volume":"233 2","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2019-06-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Clinical and hormonal features of adolescent girls with primary and secondary oligomenorrhea\",\"authors\":\"S. Levenets, N. O. Udovikova, S. Novokhatska\",\"doi\":\"10.30978/ujpe2019-2-28\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"The objective was to provide a comparative characteristic of clinical and hormonal parameters in secondary and primary oligomenorrhea (OM II and OM I) in adolescent girls. Materials and methods. A total of 185 girls with OM aged 13—17 years (142 with OM I and 43 with OM II) and 107 girls with a regular menstrual cycle (regMС — comparison group (CG)) were examined. We analyzed clinical and anamnestic indicators, data of ultrasound of the pelvic organs, LH, FSH, estradiol, and testosterone levels. Results and discussion. Family history of impaired function of the reproductive system in girls with OM II were less likely than with OM I (12.5 vs. 25.8 %; рφ < 0.002). Mothers of girls with OM gave birth more often at an early reproductive age than in CG (14.5 and 4.9 %; рφ < 0.001). Delayed menarche (15 years and later) with OM I was 5 times more frequent than in CG (24,1 vs 4,7 %; рφ< 0,001), while in OM II its frequency did not differ significantly from CG. Normal body mass index (BMI) in OM was less frequent than in women with reg MС (40.8 and 72.2 %, pφ < 0.001). In OM II, uterine hypoplasia was less common than in OM I (38.5 and 53.9 %; pφ < 0.05). Hypogonadotropinemia was more frequent with OM II than with OM I (21.6 versus 4.3 %; рφ < 0.001), and an increase in blood testosterone levels was more common with OM I than with OM II (24.1 versus 5.6 %; рφ < 0.01). Restoration of menstrual dysfunction was more frequent with OM II than with OM I (79.5 versus 63.4 %; рφ < 0.03). Conclusions . OM I is characterized by delayed menarche, hypoplasia of the uterus, family history of impaired function of the reproductive system and increased testosterone levels. OM II is associated with lack of stable normalization of menstrual function, marked hirsutism and hypogonadotropinemia.\",\"PeriodicalId\":243962,\"journal\":{\"name\":\"Ukrainian Journal of Pediatric Endocrinology\",\"volume\":\"233 2\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2019-06-28\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Ukrainian Journal of Pediatric Endocrinology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.30978/ujpe2019-2-28\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Ukrainian Journal of Pediatric Endocrinology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.30978/ujpe2019-2-28","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
摘要
目的是提供青春期女孩继发性和原发性少月经(OM II和OM I)的临床和激素参数的比较特征。材料和方法。共对185名13-17岁的OM女孩(OM I 142例,OM II 43例)和107名月经周期正常的女孩(regMС -对照组(CG))进行了检查。我们分析了临床和记忆指标、盆腔器官超声数据、LH、FSH、雌二醇和睾酮水平。结果和讨论。II型OM女孩有生殖系统功能受损家族史的可能性低于I型OM女孩(12.5% vs. 25.8%;φ < 0.002)。患有OM的女孩的母亲在育龄早期分娩的情况比患有CG的女孩多(14.5%和4.9%;φ < 0.001)。迟发性月经初潮(15年及以后)是CG的5倍(24.1 vs 4.7%;φ< 0.001),而在OM II中,其频率与CG无显著差异。正常体重指数(BMI)在OM患者中的发生率低于regMС患者(40.8%和72.2%,pφ < 0.001)。在OM II中,子宫发育不全的发生率低于OM I(38.5%和53.9%);Pφ < 0.05)。低促性腺激素血症在OM II患者中比OM I患者更常见(21.6%对4.3%; φ < 0.001),并且血液睾酮水平的升高在OM I组比OM II组更常见(24.1%比5.6%;φ < 0.01)。OM II组比OM I组更容易恢复月经功能障碍(79.5%比63.4%;φ < 0.03)。结论。OM I的特征是月经初潮延迟,子宫发育不全,生殖系统功能受损的家族史和睾酮水平升高。OM II与月经功能缺乏稳定的正常化、明显的多毛症和促性腺激素水平低下有关。
Clinical and hormonal features of adolescent girls with primary and secondary oligomenorrhea
The objective was to provide a comparative characteristic of clinical and hormonal parameters in secondary and primary oligomenorrhea (OM II and OM I) in adolescent girls. Materials and methods. A total of 185 girls with OM aged 13—17 years (142 with OM I and 43 with OM II) and 107 girls with a regular menstrual cycle (regMС — comparison group (CG)) were examined. We analyzed clinical and anamnestic indicators, data of ultrasound of the pelvic organs, LH, FSH, estradiol, and testosterone levels. Results and discussion. Family history of impaired function of the reproductive system in girls with OM II were less likely than with OM I (12.5 vs. 25.8 %; рφ < 0.002). Mothers of girls with OM gave birth more often at an early reproductive age than in CG (14.5 and 4.9 %; рφ < 0.001). Delayed menarche (15 years and later) with OM I was 5 times more frequent than in CG (24,1 vs 4,7 %; рφ< 0,001), while in OM II its frequency did not differ significantly from CG. Normal body mass index (BMI) in OM was less frequent than in women with reg MС (40.8 and 72.2 %, pφ < 0.001). In OM II, uterine hypoplasia was less common than in OM I (38.5 and 53.9 %; pφ < 0.05). Hypogonadotropinemia was more frequent with OM II than with OM I (21.6 versus 4.3 %; рφ < 0.001), and an increase in blood testosterone levels was more common with OM I than with OM II (24.1 versus 5.6 %; рφ < 0.01). Restoration of menstrual dysfunction was more frequent with OM II than with OM I (79.5 versus 63.4 %; рφ < 0.03). Conclusions . OM I is characterized by delayed menarche, hypoplasia of the uterus, family history of impaired function of the reproductive system and increased testosterone levels. OM II is associated with lack of stable normalization of menstrual function, marked hirsutism and hypogonadotropinemia.