Young Min Choi, Kyu Ri Hwang, Dayong Lee, Sunmie Kim, Jin Ju Kim
{"title":"Age-Independent Serum AMH Levels in Women With PCOS Defined by the 2018 Evidence-Based Guideline Diagnostic Criteria: A Cross-Sectional Study","authors":"Young Min Choi, Kyu Ri Hwang, Dayong Lee, Sunmie Kim, Jin Ju Kim","doi":"10.1111/cen.70000","DOIUrl":"10.1111/cen.70000","url":null,"abstract":"<div>\u0000 \u0000 \u0000 <section>\u0000 \u0000 <h3> Objective</h3>\u0000 \u0000 <p>The 2018 evidence-based guideline revised the follicle count threshold for polycystic ovary morphology (PCOM) from ≥ 12 to ≥ 20, thereby introducing a stricter definition than the Rotterdam criteria. In 2023, anti-Müllerian hormone (AMH) was incorporated into defining PCOM. Although PCOS-related symptoms often improve with age, some women continue to exhibit symptoms and meet the PCOS diagnostic criteria even as they age. This study examined AMH patterns across age groups in women who already met the PCOS diagnostic criteria according to either the Rotterdam or the stricter 2018 criteria.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Methods</h3>\u0000 \u0000 <p>This cross-sectional study included 725 women diagnosed with PCOS according to the Rotterdam criteria, of whom 520 also fulfilled the 2018 criteria. Serum AMH levels were compared across age groups: < 25, 25–34.9, and 35–45 years.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Results</h3>\u0000 \u0000 <p>Among women meeting the Rotterdam criteria, AMH levels were significantly lower in the oldest group (9.0 ng/mL) than in those < 25 years (11.2 ng/mL, <i>p</i> = 0.032). Meanwhile, among women who met the 2018 criteria, mean AMH levels were 12.5, 12.0, and 10.0 ng/mL in < 25, 25–34.9, and 35–45 year groups, respectively (<i>p</i> = 0.077), with no correlation between age and AMH (<i>r</i> = −0.050, <i>p</i> = 0.178). Additionally, the oldest group showed worse metabolic profiles than the younger groups.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Conclusions</h3>\u0000 \u0000 <p>Women who continued to meet the stricter criteria at older reproductive ages showed AMH levels comparable to those of younger patients, and had worse metabolic profiles, supporting AMH as a stable diagnostic marker across reproductive ages in PCOS.</p>\u0000 </section>\u0000 </div>","PeriodicalId":10346,"journal":{"name":"Clinical Endocrinology","volume":"103 4","pages":"580-586"},"PeriodicalIF":2.4,"publicationDate":"2025-07-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/cen.70000","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144590518","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Mohammed Ashraf Ganie, Pinaki Dutta, Mohammed Sharfraz Ahamed, Imtiyaz Ahmad Wani, Neena Malhotra, Puthiyaveettil Khadar Jabbar, Rakesh Sahay, Sarita Agrawal, Roya Rozati, Vanita Suri, Subhankar Chowdhury, Prasanta Kumar Bhattacharya, Taruna Arora, Khurshid Ahmad Padder, Rabiya Rashid, Khalid Ul Islam Rather
{"title":"Unravelling Prevalence and Pattern of Various Hormonal Dysfunctions Among Reproductive Age Community Dwelling Indian Women: Lessons From ICMR PCOS Task Force Sub Study","authors":"Mohammed Ashraf Ganie, Pinaki Dutta, Mohammed Sharfraz Ahamed, Imtiyaz Ahmad Wani, Neena Malhotra, Puthiyaveettil Khadar Jabbar, Rakesh Sahay, Sarita Agrawal, Roya Rozati, Vanita Suri, Subhankar Chowdhury, Prasanta Kumar Bhattacharya, Taruna Arora, Khurshid Ahmad Padder, Rabiya Rashid, Khalid Ul Islam Rather","doi":"10.1111/cen.15297","DOIUrl":"10.1111/cen.15297","url":null,"abstract":"<div>\u0000 \u0000 \u0000 <section>\u0000 \u0000 <h3> Background</h3>\u0000 \u0000 <p>Population-specific studies examining the prevalence of endocrine dysfunctions among Indian women are limited. Therefore, we analysed the data of the multicentric and multiregional National ICMR-PCOS task force study to evaluate the magnitude and pattern of endocrine dysfunctions among women of reproductive age group across various zones of India.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Methods</h3>\u0000 \u0000 <p>Women aged 18−40 years (<i>N</i> = 12,100) were approached from five zones of the country including both rural and urban areas and were evaluated using multistage cluster design based on 2011 census. A structured uniform questionnaire capturing details of medical history, drug intake and so on. was collected, followed by relevant physical examination, laboratory assessment (blood counts, liver, and kidney function tests), hormonal panel (serum LH, FSH, PRL, total testosterone, 17OHP, SHBG, DHEAS, insulin, T4, TSH, Cortisol) and abdominal ultrasound.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Results</h3>\u0000 \u0000 <p>Out of the 12,100 subjects listed in the Voter ID list and approached at all the participating sites, 831 declined to participate, and 2276 were deemed ineligible. The screening questionnaire was administered to a total of 8993 women. The study showed a remarkably high prevalence of oligo-anovulation (21.5%), closely followed by clinical hyperandrogenism (21%). Biochemical hyperandrogenism and subclinical hypothyroidism emerged as the most prevalent endocrine dysfunctions (15.6%).</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Conclusion</h3>\u0000 \u0000 <p>This nationally representative study is probably the first global study to report the various endocrine dysfunctions in reproductive age women and will help in formulating national health policies.</p>\u0000 </section>\u0000 </div>","PeriodicalId":10346,"journal":{"name":"Clinical Endocrinology","volume":"103 5","pages":"714-720"},"PeriodicalIF":2.4,"publicationDate":"2025-07-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144590521","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Nyo Nyo Z. Tun, Nicola N. Zammitt, Mark W. J. Strachan, Jonathan R. Seckl, Fraser W. Gibb
{"title":"Ten Year Outcome of Anti-Thyroid Drug Treatment for First Episode Graves' Thyrotoxicosis: The Predictive Importance of TRAb","authors":"Nyo Nyo Z. Tun, Nicola N. Zammitt, Mark W. J. Strachan, Jonathan R. Seckl, Fraser W. Gibb","doi":"10.1111/cen.70003","DOIUrl":"10.1111/cen.70003","url":null,"abstract":"<div>\u0000 \u0000 \u0000 <section>\u0000 \u0000 <h3> Objective</h3>\u0000 \u0000 <p>To establish the risk and time course of recurrent thyrotoxicosis following withdrawal of anti-thyroid drugs (ATD) and risk factors for recurrence.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Design</h3>\u0000 \u0000 <p>Single-centre retrospective study.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Methods</h3>\u0000 \u0000 <p>Two hundred and ninety people with a first episode of Graves' thyrotoxicosis, who completed a course of ATD, were included. Clinical and biochemical parameters associated with recurrence risk were assessed over a 10-year period.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Results</h3>\u0000 \u0000 <p>Recurrence occurred in 54% of individuals over a 10-year period, with 73% occurring within 2 years. Younger age (41 years [33–51] vs. 47 [39–56], <i>p</i> = 0.011), higher TSH receptor antibody (TRAb) at diagnosis (8.8 IU/L [4.9−17.2] versus 6.0 [4.1−9.9], <i>p</i> = 0.002), higher TRAb at cessation of ATD (1.3 [<0.9–2.3] vs. 1.0 [<0.9–1.3], <i>p</i> < 0.001), longer time to normalisation of TSH (6 months [3–9] vs. 4 [2–7], <i>p</i> 0.013) and longer time to normalisation of fT4 (2 months [1−3] vs. 1 [1−2], <i>p</i> = 0.001) were all associated with relapse within 10 years. Recurrence within 10 years occurred in 74% of individuals with TRAb > 12 IU/L at diagnosis but only 44% of those with TRAb < 5 IU/L at diagnosis (<i>p</i> = 0.001). TRAb (at diagnosis and cessation) and age were independently associated with relapse in multivariate analysis.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Conclusions</h3>\u0000 \u0000 <p>Most recurrent thyrotoxicosis occurs within the first few years after ATD withdrawal. TRAb concentration, at diagnosis and cessation of ATD, is a useful predictor of recurrence risk and can be used to inform decisions on the optimal approach to primary therapy.</p>\u0000 </section>\u0000 </div>","PeriodicalId":10346,"journal":{"name":"Clinical Endocrinology","volume":"103 4","pages":"612-618"},"PeriodicalIF":2.4,"publicationDate":"2025-07-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/cen.70003","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144590520","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Safety of Cabergoline for Prolactinoma in Pregnancy: A Systematic Review and Meta-Analysis","authors":"Ananda Mohan Chakraborty, Ashu Rastogi","doi":"10.1111/cen.15304","DOIUrl":"10.1111/cen.15304","url":null,"abstract":"<div>\u0000 \u0000 \u0000 <section>\u0000 \u0000 <h3> Introduction</h3>\u0000 \u0000 <p>Prolactinoma is commonly treated with cabergoline, a dopamine D2 agonist. The present systematic review and meta-analysis aimed to assess the safety of cabergoline during pregnancy by examining outcomes of fetal loss, congenital malformations, preterm delivery, low birth weight, and change of tumour size post-gestation.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Method</h3>\u0000 \u0000 <p>We conducted a systematic review as per PRISMA guidelines, focusing on pregnant patients with prolactinoma. Using the PICO model, we analyzed pregnancy outcomes in women continued cabergoline during gestation versus discontinuation at pregnancy diagnosis. Our methodologies included data extraction, study selection, and outcome analysis.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Results</h3>\u0000 \u0000 <p>A total of 12 studies mentioning 1387 pregnancies with prolactinoma were included. Fetal loss occurred in 16.1% of cases, while congenital malformations were observed in 4.7%. The live birth rates among cabergoline users during gestation were lower compared to non-users [RR 0.81 (0.67–0.98, 95% CI); <i>p</i> = 0.03]. The congenital malformations [0.99 (95% CI: 0.93–1.07); <i>p</i> = 0.88], preterm birth [RR: 1.00 (95% CI: 0.93–1.07); <i>p</i> = 0.97] and low birth weight [RR: 1.02 (95% CI: 0.90–1.16); <i>p</i> = 0.71] showed no differences between the two groups.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Conclusion</h3>\u0000 \u0000 <p>Cabergoline, when continued during pregnancy, is associated with a lower chance of live birth compared to discontinuation of pregnancy at diagnosis of pregnancy in women with prolactinoma. However, there was no increased risk of incident congenital malformation, preterm birth or low birth weight. The analysis suggests careful consideration of cabergoline use in pregnant women with prolactinoma.</p>\u0000 </section>\u0000 </div>","PeriodicalId":10346,"journal":{"name":"Clinical Endocrinology","volume":"103 5","pages":"633-640"},"PeriodicalIF":2.4,"publicationDate":"2025-07-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/cen.15304","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144590519","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Nonobese PCOS Compared to Obese PCOS Have Similar Clinical Presentation, Hormonal Profile, and Insulin Resistance","authors":"Pankaj Patwari, Nisha Batra, Kaushik Sen, Ankita Saha, Binita Kumari, Madhurima Basu, Souveek Mitra, Kausik Das, Gaurishankar Kamilya, Arjun Baidya, Animesh Maiti, Debasis Bhattacharyya, Pradip Mukhopadhyay, Sujoy Ghosh","doi":"10.1111/cen.15302","DOIUrl":"10.1111/cen.15302","url":null,"abstract":"<div>\u0000 \u0000 \u0000 <section>\u0000 \u0000 <h3> Introduction</h3>\u0000 \u0000 <p>Ethnicity-based BMI and WC cut-offs are used to group PCOS into obese and nonobese PCOS. Uncertainty exists regarding differences in clinical presentation, body composition, hepatic fat, insulin resistance (especially in comparison to visceral fat), and adiposopathy between obese and nonobese PCOS.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Materials and Methods</h3>\u0000 \u0000 <p>This was an observational study wherein we evaluated women 18–40 years of age and compared Obese PCOS (OP) with nonobese PCOS (NOP) and additionally compared them with obese controls without PCOS (OC) and nonobese control without PCOS (NOC) (30 subjects in each group), with respect to their clinical, biochemical, hormonal cyto-adipokines/hepatokines, body composition by DXA, transient hepatic elastography, and insulin sensitivity with disposition index using frequently sampled Intravenous Glucose Tolerance Test (fsIVGTT).</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Results</h3>\u0000 \u0000 <p>Nonobese PCOS subjects were more likely to have menstrual irregularities, compared to obese PCOS (93% vs. 70%, <i>p</i> = 0.02). Serum testosterone, LH/FSH, SHBG visceral adipose tissue content, insulin resistance (disposition index on fsIVGTT), and all pro-inflammatory cytokines (IL-6, IL-8, IL-1β), except TNF-α (17.7 vs. 11.5 pg/ml, <i>p</i> = 0.001), were found to be similar between obese and nonobese PCOS groups. Fasting plasma glucose was slightly higher (89 vs. 79 mg/dl, <i>p</i> = 0.02) in obese PCOS as compared to non-obese PCOS group. PCOS subjects had significantly higher body fat%, visceral fat and android gynoid ratio than BMI-matched controls (<i>p</i> = < 0.001). Corrected VAT was similar in obese vs. nonobese PCOS. PCOS subjects had higher hepatic fat content & insulin resistance in comparison to BMI-matched healthy controls (<i>p</i>-value 0.03 and 0.02 respectively).</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Conclusion</h3>\u0000 \u0000 <p>Obese and nonobese PCOS subjects overall appear to share similar biochemical hormonal correct VAT, and insulin resistance.</p>\u0000 </section>\u0000 </div>","PeriodicalId":10346,"journal":{"name":"Clinical Endocrinology","volume":"103 4","pages":"567-579"},"PeriodicalIF":2.4,"publicationDate":"2025-07-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144583249","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Stella Pigni, Walter Vena, Maria Francesca Birtolo, Alessandro Fanti, Fabio Massimo Ulivieri, Luca Rinaudo, Lorenzo Leonardi, Luca Balzarini, Antonio Carlo Bossi, Alessandro Pizzocaro, Andrea Lania, Gherardo Mazziotti
{"title":"Unraveling the Puzzle of Bone Health in Klinefelter Syndrome: Association Between DXA-Derived Lumbar Bone Strain Index and Body Composition Parameters in a Single Center Cohort","authors":"Stella Pigni, Walter Vena, Maria Francesca Birtolo, Alessandro Fanti, Fabio Massimo Ulivieri, Luca Rinaudo, Lorenzo Leonardi, Luca Balzarini, Antonio Carlo Bossi, Alessandro Pizzocaro, Andrea Lania, Gherardo Mazziotti","doi":"10.1111/cen.15301","DOIUrl":"10.1111/cen.15301","url":null,"abstract":"<div>\u0000 \u0000 \u0000 <section>\u0000 \u0000 <h3> Objective</h3>\u0000 \u0000 <p>Klinefelter syndrome (KS) is frequently characterized by skeletal fragility with increased risk of fractures, independently of testosterone levels and bone mineral density (BMD). Unfavorable body composition might negatively influence bone health in KS patients. Recently, a new dual-energy <i>X</i>-ray absorptiometry (DXA)-derived index of bone strength, the bone strain index (BSI), has emerged as a promising tool for assessing fracture risk and bone quality derangement, particularly in secondary osteoporosis. The aim of this study was to investigate the associations between lumbar BSI (<span>l</span>-BSI), trabecular bone score (TBS) and body composition parameters in a cohort of adult patients with KS.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Design</h3>\u0000 \u0000 <p>Cross-sectional study.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Patients</h3>\u0000 \u0000 <p>Forty four patients with 47, XXY KS (median age 39.5 years, range 18–61) followed at an Italian referral center.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Measurements</h3>\u0000 \u0000 <p>BMD, BSI, TBS, and body composition parameters were evaluated by total body DXA. Correlations between body composition and bone parameters were analyzed.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Results</h3>\u0000 \u0000 <p><span>l</span>-BSI was significantly associated with fat mass index (FMI) (rho = 0.64, <i>p</i> < 0.001), fat-to-lean mass index ratio (rho = 0.66, <i>p</i> < 0.001), and visceral fat mass (rho = 0.56, <i>p</i> < 0.001). A strong negative correlation between <span>l</span>-BSI and TBS (rho: −0.73, <i>p</i> < 0.001) was also observed. Patients with impaired TBS and those with later age at KS diagnosis showed significantly higher <span>l</span>-BSI values (<i>p</i> < 0.001). Later age at KS diagnosis also correlated with higher body fat indexes.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Conclusions</h3>\u0000 \u0000 <p>Increased adiposity may have detrimental effects on lumbar bone quality and strength as assessed by <span>l</span>-BSI in adult patients with KS. Later diagnosis of KS may contribute to unfavorable body composition and impaired skeletal health.</p>\u0000 </section>\u0000 </div>","PeriodicalId":10346,"journal":{"name":"Clinical Endocrinology","volume":"103 4","pages":"463-470"},"PeriodicalIF":2.4,"publicationDate":"2025-07-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144574943","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Sofia Anelli, Rossella Mazzilli, Virginia Zamponi, Beatrice Giorgini, Bianca Golisano, Camilla Mancini, Flaminia Russo, Francesco Panzuto, Antongiulio Faggiano
{"title":"Glucagonoma and Glucagonoma Syndrome: An Updated Review","authors":"Sofia Anelli, Rossella Mazzilli, Virginia Zamponi, Beatrice Giorgini, Bianca Golisano, Camilla Mancini, Flaminia Russo, Francesco Panzuto, Antongiulio Faggiano","doi":"10.1111/cen.15300","DOIUrl":"10.1111/cen.15300","url":null,"abstract":"<div>\u0000 \u0000 \u0000 <section>\u0000 \u0000 <h3> Background</h3>\u0000 \u0000 <p>Glucagonoma is a rare well-differentiated slowly proliferating pancreatic neuroendocrine tumour, characterized by several manifestations including necrolytic migratory erythema, weight loss, diabetes and anaemia.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Aim</h3>\u0000 \u0000 <p>The purpose of the current review was to acknowledge literature about this rare tumour discerning the clinical features, diagnosis, treatment and prognosis of glucagonoma by comparing three different periods.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Results</h3>\u0000 \u0000 <p>A study published by Song reviewed 216 cases from studies published between 1999 and 2016, making a comparison with 407 cases reported before 1998 by Soga and Yakuwa. The current review consisted of 86 cases reported in studies published in and after 2017: 40 males and 46 females, with an average age of 48.2 years. The male-to-female ratio was 0.87. The rate of typical clinical findings was as follows: NME, 93.2% (69/74); DM, 70.3% (50/74); weight loss, 62.2% (46/74); anaemia, 44.6% (33/74); glossitis or stomatitis or cheilitis, 31.1% (23/74). A total of 85 cases reported the location of the tumour as the pancreas and 38.8% of these cases involved the tail of the pancreas. The average tumour size was 4.6 cm in patients between 2017 and 2024. Metastasis was detected in 52.3% of patients (45/86). The comparison with previous series highlighted an earlier age of diagnosis of glucagonoma and a higher rate of NME, consistent with a higher diagnostic accuracy.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Conclusions</h3>\u0000 \u0000 <p>Glucagonoma is a rare pathology, with peculiar characteristics that need to be acknowledged to achieve a timely diagnosis and finally improve patient prognosis.</p>\u0000 </section>\u0000 </div>","PeriodicalId":10346,"journal":{"name":"Clinical Endocrinology","volume":"103 4","pages":"417-426"},"PeriodicalIF":2.4,"publicationDate":"2025-07-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/cen.15300","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144559394","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Marianne Lucena da Silva, Nádia Martins de Paula Souza, Miguel Luciano Rodrigues da Silva Júnior, Brenda Gabriele Dantas Pinto Vieira, Liana Barbaresco Gomide Matheus, Aline Teixeira Alves, Katiane da Costa Cunha
{"title":"Evaluation of Cardiac Autonomic Function in Patients With Alteration in Thyroid Hormones: Systematic Literature Review","authors":"Marianne Lucena da Silva, Nádia Martins de Paula Souza, Miguel Luciano Rodrigues da Silva Júnior, Brenda Gabriele Dantas Pinto Vieira, Liana Barbaresco Gomide Matheus, Aline Teixeira Alves, Katiane da Costa Cunha","doi":"10.1111/cen.15299","DOIUrl":"10.1111/cen.15299","url":null,"abstract":"<div>\u0000 \u0000 \u0000 <section>\u0000 \u0000 <h3> Background</h3>\u0000 \u0000 <p>Thyroid hormonal disorders are widely discussed in the literature. These dysfunctions also influence the modulation of the cardiovascular system due to alterations in the autonomic nervous system, affecting heart rate variability.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Objectives</h3>\u0000 \u0000 <p>To verify the influence of thyroidian hormonal dysfunctions on the modulation of cardiac autonomic activity.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Methods</h3>\u0000 \u0000 <p>A systematic review was carried out to search for studies used in the electronic databases Virtual Health Library (VHL), Scielo, Pubmed via Medline, Cochrane, Embase, Scopus, Web of Science, Cinahl and SPORTDiscus, without restrictions how many years. For this review, we have considered experimental studies carried out with human beings that will analyse the variability of heart rate in the thyroid hormone diseases.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Results</h3>\u0000 \u0000 <p>Ten thousand two hundred ninety-eight items found, 15 included, which were non-randomised clinical trials that assessed heart rate variability domains. I note that patients affected by hypothyroidism or hyperthyroidism have a reduction in heart rate variability, reflecting a decrease in the adaptive capacity of the heart.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Conclusion</h3>\u0000 \u0000 <p>Both hypothyroidism and hyperthyroidism affect cardiac autonomic modulation, resulting in a reduction in heart rate variability. However, there were differences in relation to the availability of frequency and time data.</p>\u0000 </section>\u0000 </div>","PeriodicalId":10346,"journal":{"name":"Clinical Endocrinology","volume":"103 4","pages":"407-416"},"PeriodicalIF":2.4,"publicationDate":"2025-07-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/cen.15299","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144559393","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Clinical Characteristics of KMT2A Gene-Related Wiedemann–Steiner Syndrome and Progress in Recombinant Human Growth Hormone Therapy for Short-Stature Children","authors":"Xinyu Yue, Meiping Chen, Xiaoan Ke, Hongbo Yang, Fengying Gong, Linjie Wang, Lian Duan, Hui Pan, Huijuan Zhu","doi":"10.1111/cen.15293","DOIUrl":"10.1111/cen.15293","url":null,"abstract":"<div>\u0000 \u0000 \u0000 <section>\u0000 \u0000 <h3> Objective</h3>\u0000 \u0000 <p>Wiedemann–Steiner syndrome (WSS) due to <i>KMT2A</i> variant is a rare autosomal dominant genetic heterogeneity disorder associated with short stature, the exact genetic mechanism of which is still unknown. This study aims to define the clinical, therapeutic and molecular findings of three new WSS patients from unrelated families, and to summarize the clinical characteristics and response to recombinant human growth hormone (rhGH) therapy.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Design, Patients and Measurements</h3>\u0000 \u0000 <p>Three male patients with short stature were included, and whole-exome sequencing (WES) was performed. All reported patients with WSS worldwide caused by <i>KMT2A</i> variants were reviewed.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Results</h3>\u0000 \u0000 <p>The average age of the three patients was 8.3 ± 8.9 years, with an average height <i>Z</i>-score of −3.9 ± 1.8. Three <i>KMT2A</i> variants were detected with the aid of WES. A total of 333 cases of WSS have been reported, with 269 types of <i>KMT2A</i> gene variants described. WSS was characterized by intellectual disorder (92.9%, 250/269), developmental delay (87.9%, 175/199), generalized hypertrichosis (76.7%, 66/86) and short stature (70.9%, 61/86). The height <i>Z</i>-score of 14 patients received rhGH treatment significantly increased from −3.3 ± 1.2 to −1.8 ± 1.0 (<i>p</i> < 0.001) after an average treatment duration of 25.7 ± 23.1 months, and was positively correlated with the duration of treatment (<i>r</i> = 0.899, <i>p</i> < 0.0001). There was no significant difference in the height <i>Z</i>-score change between seven growth hormone deficiency (GHD) patients and five non-GHD patients after rhGH treatment.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Conclusions</h3>\u0000 \u0000 <p>This study provided a comprehensive analysis between phenotypes and genotypes of <i>KMT2A</i> variants and WSS. Our findings indicated that patients with WSS may experience favourable outcomes with rhGH therapy.</p>\u0000 </section>\u0000 </div>","PeriodicalId":10346,"journal":{"name":"Clinical Endocrinology","volume":"103 5","pages":"692-702"},"PeriodicalIF":2.4,"publicationDate":"2025-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144539232","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Prevalence of Primary Aldosteronism Among Patients With Hypertension","authors":"Divyansh Goyal, Manasvini Bhatt, Tamoghna Ghosh, Prayas Sethi, Ranveer Singh Jadon, Sarah Alam, Rajesh Khadgawat","doi":"10.1111/cen.15296","DOIUrl":"10.1111/cen.15296","url":null,"abstract":"<div>\u0000 \u0000 \u0000 <section>\u0000 \u0000 <h3> Background</h3>\u0000 \u0000 <p>Despite being a leading cause of secondary hypertension and association with a higher incidence of cardiovascular morbidity and mortality the prevalence of primary aldosteronism (PA) is poorly studied.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Objective</h3>\u0000 \u0000 <p>We assessed the prevalence of PA in participants being treated as essential hypertension (EHTN).</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Design and Participants</h3>\u0000 \u0000 <p>In this prospective, cross-sectional study, 492 participants with diagnosis of EHTN were evaluated. The screening for PA was conducted by measuring plasma aldosterone concentration (PAC) and direct renin concentration (DRC), from which the aldosterone-to-renin ratio (ARR) was calculated. Based on Endocrine Society guidelines, screening test was followed by a confirmatory recumbent saline infusion test (SIT). Participants who showed a post-SIT PAC greater than 5 ng/dL were diagnosed with PA.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Results</h3>\u0000 \u0000 <p>Of 492 EHTN participants, 91 (18.49%) had positive screening test. Out of 91 participants, 59 agreed for SIT and PA was confirmed in 37 participants (8.04%) (Excluding 32 screened positive participants who were non-compliant to SIT). The mean age was 49.98 ± 7.76 years, and median duration of hypertension was 5 (0−24) years. The prevalence of PA increased with grade of hypertension (5.97% in grade 1%−12.03% in grade 3), hypertension daily dose (HDD) (3.57% in those with HDD < 1% to 27.27% in those with HDD ≥ 4). No significant difference in hypokalaemia in PA and EHTN (2.70% and 3.54% respectively, <i>p</i>: 0.7815).</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Conclusions</h3>\u0000 \u0000 <p>Our study shows a high prevalence of PA in subjects treated as a case of EHTN.</p>\u0000 </section>\u0000 </div>","PeriodicalId":10346,"journal":{"name":"Clinical Endocrinology","volume":"103 4","pages":"447-455"},"PeriodicalIF":2.4,"publicationDate":"2025-06-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144526649","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}