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<article article-type="research-article" dtd-version="1.3" xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xml:lang="ru"><front><journal-meta><journal-id journal-id-type="publisher-id">problendo</journal-id><journal-title-group><journal-title xml:lang="ru">Проблемы Эндокринологии</journal-title><trans-title-group xml:lang="en"><trans-title>Problems of Endocrinology</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">0375-9660</issn><issn pub-type="epub">2308-1430</issn><publisher><publisher-name>Endocrinology Research Centre</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.14341/probl13419</article-id><article-id custom-type="elpub" pub-id-type="custom">problendo-13419</article-id><article-categories><subj-group subj-group-type="heading"><subject>Research Article</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="ru"><subject>Детская эндокринология</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>Pediatric Endocrinology</subject></subj-group></article-categories><title-group><article-title>Новый способ дифференциальной диагностики гипогонадотропного гипогонадизма и конституциональной задержки полового развития у юношей 13,5–17 лет</article-title><trans-title-group xml:lang="en"><trans-title>A new way for the differential diagnosis of hypogonadotropic hypogonadism and constitutional delay of puberty in adolescent men aged 13.5–17 years</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-7906-7408</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Скородок</surname><given-names>Ю. Л.</given-names></name><name name-style="western" xml:lang="en"><surname>Skorodok</surname><given-names>Y. L.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Скородок Юлия Леонидовна, к.м.н., доцент</p><p>Санкт-Петербург</p></bio><bio xml:lang="en"><p>Yulia L. Skorodok, PhD, MD</p><p>Saint-Petersburg</p></bio><email xlink:type="simple">julia_skorodok@mail.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0009-0004-5409-234X</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Иоффе</surname><given-names>И. Ю.</given-names></name><name name-style="western" xml:lang="en"><surname>Ioffe</surname><given-names>I. Y.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Иоффе Ирина Юрьевна</p><p>194100, Санкт-Петербург, улица Литовская, д. 2</p></bio><bio xml:lang="en"><p>Irina Y. Ioffe, MD</p><p>2 Litovskaya street, 194100, Saint-Peterburg</p></bio><email xlink:type="simple">ioffe.i@bk.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-1104-7368</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Плотникова</surname><given-names>Е. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Plotnikova</surname><given-names>E. V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Плотникова Елена Валерьевна, к.м.н.</p><p>Санкт-Петербург</p></bio><bio xml:lang="en"><p>Elena V. Plotnikova, PhD, MD</p><p>Saint-Petersburg</p></bio><email xlink:type="simple">miss-plotnicko@yandex.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-6190-9256</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Нагорная</surname><given-names>И. И.</given-names></name><name name-style="western" xml:lang="en"><surname>Nagornaya</surname><given-names>I. I.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Нагорная Ирена Игоревна, к.м.н.</p><p>Санкт-Петербург</p></bio><bio xml:lang="en"><p>Irena I. Nagornaya, PhD, MD</p><p>Saint-Petersburg</p></bio><email xlink:type="simple">irena_nagornaya@mail.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-8474-5154</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Желенина</surname><given-names>Л. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Zhelenina</surname><given-names>L. A.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Желенина Людмила Александровна, д.м.н., профессор</p><p>Санкт-Петербург</p></bio><bio xml:lang="en"><p>Liudmila A. Zhelenina, MD, PhD, Professor</p><p>Saint-Petersburg</p></bio><email xlink:type="simple">jelenina@mail.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0009-0003-8784-5224</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Кожевникова</surname><given-names>А. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Kozhevnikova</surname><given-names>A. V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Кожевникова Анжелика Владимировна</p><p>Санкт-Петербург</p></bio><bio xml:lang="en"><p>Anzhelika V. Kozhevnikova, MD</p><p>Saint-Petersburg</p></bio><email xlink:type="simple">angelochik2101@mail.ru</email><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>Санкт-Петербургский государственный педиатрический медицинский университет</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Saint-Petersburg state pediatric medical university</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2024</year></pub-date><pub-date pub-type="epub"><day>09</day><month>03</month><year>2024</year></pub-date><volume>70</volume><issue>6</issue><fpage>106</fpage><lpage>117</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Скородок Ю.Л., Иоффе И.Ю., Плотникова Е.В., Нагорная И.И., Желенина Л.А., Кожевникова А.В., 2025</copyright-statement><copyright-year>2025</copyright-year><copyright-holder xml:lang="ru">Скородок Ю.Л., Иоффе И.Ю., Плотникова Е.В., Нагорная И.И., Желенина Л.А., Кожевникова А.В.</copyright-holder><copyright-holder xml:lang="en">Skorodok Y.L., Ioffe I.Y., Plotnikova E.V., Nagornaya I.I., Zhelenina L.A., Kozhevnikova A.V.</copyright-holder><license xml:lang="ru" license-type="creative-commons-attribution" xlink:href="https://creativecommons.org/licenses/by/4.0/" xlink:type="simple"><license-p>Данная работа распространяется под лицензией Creative Commons Attribution 4.0.</license-p></license><license xml:lang="en" license-type="creative-commons-attribution" xlink:href="https://creativecommons.org/licenses/by/4.0/" xlink:type="simple"><license-p>This work is licensed under a Creative Commons Attribution 4.0 License.</license-p></license></permissions><self-uri xlink:href="https://www.probl-endojournals.ru/jour/article/view/13419">https://www.probl-endojournals.ru/jour/article/view/13419</self-uri><abstract><p>ОБОСНОВАНИЕ. Дифференциальная диагностика гипогонадотропного гипогонадизма (ГГ) и конституциональной задержки полового развития (КЗПР) крайне важна, так как при последней половое созревание начинается и полностью завершается без какого-либо медицинского вмешательства, а при первом пубертатный период не наступает либо проходит не до конца, и отсутствие своевременного лечения приводит к медицинской и психосоциальной дезадаптации.ЦЕЛЬ. Разработка метода дифференциальной диагностики гипогонадотропного гипогонадизма и конституциональной задержки полового развития у юношей 13,5–17 лет путем балльной оценки уровней лютеинизирующего гормона, фолликулостимулирующего гормона, тестостерона и ингибина В.МАТЕРИАЛЫ И МЕТОДЫ. Целевую популяцию формировали из юношей 13,5–17 лет с синдромом задержки пубертата путем сплошного включения наблюдений. Оценивали анамнестические данные, стадию пубертата, объем тестикул; определяли сывороточные уровни ЛГ, ФСГ, тестостерона (Т) методом хемилюминисцентного анализа, ингибина В, АМГ–ИФА. Проводили стимуляционные тесты с трипторелином и 3-дневным введением хорионического гонадотропина. Пациентов наблюдали амбулаторно в течение 6–24 месяцев.РЕЗУЛЬТАТЫ. В исследование включили юношей 13,5–17 лет с синдромом задержки пубертата: 56 — с целью создания метода дифференциальной диагностики, 30 — его контроля (группа контроля). Разработали количественный способ, позволяющий дифференцировать ГГ и КЗПР. На основании проведенного ROC-анализа установили наиболее чувствительные и специфичные маркеры ГГ и выбрали из них доступные для амбулаторного исследования базальные уровни ЛГ, ФСГ, Т, ингибина В. Для каждого показателя, основываясь на результатах собственного исследования и данных литературы, подобрали интервалы значений, в зависимости от них — оценки ЛГ, ФСГ, Т и ингибина В, а также коэффициенты (k) для каждого показателя. Баллы вычисляли путем умножения оценки на k, после чего суммировали и нормализовали к максимальной сумме, которую мог получить пациент. Для повышения точности диагностики ввели возрастной коэффициент. Итогом вычисления стал результат балльной оценки (S). S при КЗПР (10,65 [3,13–14,91]) статистически значимо отличался от такового при ГГ (76,46 [57,79–83,74]) (p&lt; 0,001). Поставленные на основании S (&lt;21,16 и ≥55,07) диагнозы в группе контроля подтверждены данными катамнеза в 97% случаев. Разработан алгоритм дифференциальной диагностики ГГ и КЗПР с использованием S.ЗАКЛЮЧЕНИЕ. Результат балльной оценки уровней ЛГ, ФСГ, тестостерона, ингибина В ≥55,07 позволяет диагностировать гипогонадотропный гипогонадизм, &lt; 21,16 — конституциональную задержку полового развития с высокой вероятностью. В случае суммы баллов ≥21,16, но &lt; 55,07 требуется расчет отношения ингибин В/АМГ и/или проведение стимуляционных тестов.</p></abstract><trans-abstract xml:lang="en"><p>BACKGROUND: Differential diagnosis of hypogonadotropic hypogonadism (HH) and constitutional delay of puberty (CDP) is extremely important since with the latter puberty begins and completes without any medical intervention and in the case of HH puberty does not occur or is incomplete. Failure to start treatment on time leads to medical and psychosocial maladjustment of the patient.AIM: Development of a method for differential diagnosis of hypogonadotropic hypogonadism and constitutional delay of puberty in boys 13.5–17 years old by scoring the levels of LH, FSH, testosterone and inhibin B.MATERIALS AND METHODS: The study group was formed by adolescent men 13.5–17 years old with delayed puberty including all observations. Anamnesis, stage of puberty, testicular volume were assessed; serum levels of LH, FSH, testosterone (T) were determined by chemiluminescent analysis and inhibin B, AMH by ELISA. Stimulation tests were performed with triptorelin and human chorionic gonadotropin (3 days). Patients were followed up for 6–24 months.RESULTS: The study included adolescent men at the age of 13.5–17 years with delayed puberty: 56 for the purpose of development a method of differential diagnosis, 30 for its control (control group). We`ve created a method that allows differentiate HH and CDP. Through the ROC-analysis the most sensitive and specific HH markers were identified. The basal levels of LH, FSH, T, and inhibin B were selected as most available for outpatient testing. Based on the results of our own research and scientific data we selected ranges of values and rated LH, FSH, T and inhibin B depending on them (marks). Then we assigned the coefficients (k) for each hormone. Scores were calculated by multiplying the marks by k then summed and normalized to the maximum amount the patient could get. To increase the accuracy of diagnosis an age coefficient was introduced. The result of the calculation was the result of the scoring (S). S for CDP (10.65 [3.13–14.91]) differed significantly from that for HH (76.46 [57.79–83.74]) (p&lt; 0.001). Diagnoses based on S (&lt;21.16 and ≥55.07) in the control group were confirmed by follow up data in 97% cases. An algorithm for the differential diagnosis of HH and CDP by using S has been developed.CONCLUSION: The result of scoring of LH, FSH, testosterone, inhibin B levels ≥55.07 makes it possible to diagnose hypogonadotropic hypogonadism, &lt; 21.16 — constitutional delay of puberty with a high probability. In the case of score ≥21.16 but &lt; 55.07, calculation of the inhibin B/AMH ratio and/or stimulation tests are required.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>гипогонадотропный гипогонадизм</kwd><kwd>юноши</kwd><kwd>синдром задержки пубертата</kwd><kwd>дифференциальная диагностика</kwd></kwd-group><kwd-group xml:lang="en"><kwd>hypogonadotropic hypogonadism</kwd><kwd>adolescent men</kwd><kwd>delayed puberty</kwd><kwd>differential diagnosis</kwd></kwd-group></article-meta></front><back><ref-list><ref id="cit1"><mixed-citation publication-type="commun" publication-format="web"><article-title>Federal'nye klinicheskie rekomendatsii (protokoly) po vedeniyu detei s endokrinnymi zabolevaniyami</article-title> / Pod red. I.I. Dedova, V.A. 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