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Uncovering hidden vitamin D deficiency in overweight children. 揭示超重儿童隐藏的维生素D缺乏症。
Pub Date : 2025-12-09 DOI: 10.5409/wjcp.v14.i4.110357
Chandra Sekhar Devulapalli

Vitamin D deficiency is disproportionately prevalent among overweight and obese children, with conventional explanations such as poor dietary intake or reduced sun exposure offering only partial insight. Emerging evidence reveals a multifactorial pathophysiology, including sequestration of vitamin D in adipose tissue, altered hepatic metabolism, diminished bioavailability, and inflammation-induced resistance at the tissue level. These mechanisms contribute to a functional deficiency, wherein serum 25-hydroxyvitamin D levels may remain suboptimal despite adequate intake or sun exposure. Obesity-related alterations in vitamin D-binding proteins, receptor expression, and pro-inflammatory signaling further compromise biological activity. Current diagnostic criteria and supplementation guidelines do not fully reflect these physiological complexities, leading to underdiagnosis and insufficient treatment. Personalized approaches-incorporating higher, body composition-adjusted dosing and consideration of inflammatory status-are emerging as promising strategies to restore sufficiency and improve metabolic outcomes. While preliminary evidence supports the safety and efficacy of high-dose supplementation in this population, pediatric-specific clinical trials are lacking. This review synthesizes current understanding of the pathophysiological mechanisms underlying vitamin D deficiency in pediatric obesity and emphasizes the need for individualized, evidence-based interventions to optimize vitamin D status and overall health.

维生素D缺乏症在超重和肥胖儿童中尤为普遍,传统的解释,如饮食摄入不足或阳光照射减少,只能提供部分解释。越来越多的证据表明,这是一个多因素的病理生理过程,包括脂肪组织中维生素D的隔离、肝脏代谢的改变、生物利用度的降低以及组织水平上炎症诱导的抵抗。这些机制导致功能性缺陷,其中血清25-羟基维生素D水平可能保持在次优水平,尽管有足够的摄入或阳光照射。肥胖相关的维生素d结合蛋白、受体表达和促炎信号的改变进一步损害了生物活性。目前的诊断标准和补充指南没有充分反映这些生理复杂性,导致诊断不足和治疗不足。个性化的方法-结合更高的,调整身体成分的剂量和考虑炎症状态-正在成为恢复充足性和改善代谢结果的有希望的策略。虽然初步证据支持高剂量补充剂在这一人群中的安全性和有效性,但缺乏针对儿科的临床试验。这篇综述综合了目前对儿童肥胖中维生素D缺乏的病理生理机制的理解,并强调需要个体化的、基于证据的干预措施来优化维生素D状态和整体健康。
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引用次数: 0
Parallel paths: A narrative review exploring autism and its co-occurring conditions. 平行路径:探索自闭症及其共同发生条件的叙事回顾。
Pub Date : 2025-12-09 DOI: 10.5409/wjcp.v14.i4.111641
Hasan Hasan, Randi Hagerman, Daphne S Say, Anh P Nguyen, Kikelomo Babata, Temitayo Oyegbile-Chidi, Angel Herrera-Guerra, Carme Torrents, Carrie E Silver, Bibiana Restrepo

Autism is a heterogeneous condition with a rising prevalence and demand for specialized care. Autistic children are more likely than neurotypical peers to experience co-occurring conditions (CCs), including medical, psychiatric, and behavioral issues, highlighting the urgent need for autism-competent healthcare providers in general healthcare. This review aims to equip primary care providers (PCPs) with a concise summary of common CCs and strategies for effective identification. A panel of experts with extensive experience in caring for autistic children collaboratively summarized key literature, research evidence, and existing clinical trial outcomes, supplementing their clinical expertise. Autistic children consistently show higher rates of both medical and mental health issues. Despite greater healthcare utilization, many autistic individuals report unmet needs. CCs can impair behavior, functioning, and well-being, but are often treatable when recognized early. Timely identification and management of medical and psychiatric CCs are critical for improving outcomes for autistic children and their families. This evidence-based review supports PCPs in enhancing their knowledge, fostering early recognition, and delivering comprehensive, responsive care.

自闭症是一种异质性疾病,发病率不断上升,需要专门护理。自闭症儿童比神经正常的同龄人更有可能经历共同发生的情况(cc),包括医学、精神和行为问题,这突出了在一般医疗保健中迫切需要有自闭症能力的医疗保健提供者。本综述旨在使初级保健提供者(pcp)对常见的cc和有效识别策略有一个简明的总结。一组在照顾自闭症儿童方面经验丰富的专家共同总结了关键文献、研究证据和现有临床试验结果,补充了他们的临床专业知识。自闭症儿童在医疗和心理健康问题上一直表现出较高的发病率。尽管医疗保健使用率更高,但许多自闭症患者报告需求未得到满足。CCs会损害行为、功能和健康,但如果及早发现,通常是可以治疗的。及时识别和管理医学和精神病学的cc对于改善自闭症儿童及其家庭的结局至关重要。这项以证据为基础的审查支持pcp提高他们的知识,促进早期识别,并提供全面的、响应性的护理。
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引用次数: 0
Approach to gallbladder polyps in pediatric patients. 小儿胆囊息肉的治疗方法。
Pub Date : 2025-12-09 DOI: 10.5409/wjcp.v14.i4.109771
Eman Al Atrash, Basil Ammori

In pediatric patients, gallbladder polyps (GBPs) are lesions that are usually found incidentally on ultrasonography, which is the first-line modality for diagnosis. Though common in adults, GBPs are rare in children, and their prevalence remains unclear. Most GBPs in children are benign, and although the risk of malignancy is influenced by polyp size, growth rate, and morphology, specific criteria for the pediatric population are lacking. Management, therefore, is based on adult guidelines, with cholecystectomy being recommended only in symptomatic patients and for rapidly enlarging or 10-mm polyps and those with unfavorable morphology to avert the risk of malignant transformation, while surveillance is applied to asymptomatic patients with smaller polyps. Further research is needed to develop pediatric-specific guidelines for the management of GBPs. This review discusses the classification, diagnosis, risk factors, and management of pediatric GBPs.

在儿科患者中,胆囊息肉(GBPs)通常是在超声检查中偶然发现的病变,这是诊断的一线方式。虽然GBPs在成人中很常见,但在儿童中很少见,其患病率尚不清楚。大多数儿童GBPs是良性的,尽管恶性肿瘤的风险受息肉大小、生长速度和形态的影响,但缺乏针对儿科人群的具体标准。因此,治疗是基于成人指南,胆囊切除术只推荐给有症状的患者,以及迅速扩大或10毫米息肉和那些形态学不良的患者,以避免恶性转化的风险,而对无症状的较小息肉患者进行监测。需要进一步的研究来制定针对GBPs管理的儿科指南。本文综述了小儿GBPs的分类、诊断、危险因素和治疗。
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引用次数: 0
Occult constipation in children: An unaddressed problem of our day-to-day practice. 儿童隐蔽性便秘:我们日常实践中未解决的问题。
Pub Date : 2025-12-09 DOI: 10.5409/wjcp.v14.i4.109590
M D Benzamin, Md Ziaur Rahman Chowdhury, Pranto Chakroborty, Akhlaq Ahmed, Tuhin Barua Tamal, Tanmoy Deb, Asm Bazlul Karim

Background: In our day-to-day practice, constipation is a common problem in the pediatric population and cause of frequent visit in outpatient and emergency department. But occult constipation (OC) remains as the most unaddressed problem.

Aim: To investigate the clinical profile of OC in children.

Methods: It was a prospective observational study, done in Bangladesh from January 2022 to December 2024. It included all consecutive children diagnosed as OC and were treated accordingly. Before diagnosis, secondary causes of the presenting symptoms were excluded with appropriate investigations. They were followed up monthly for 4 months and treatment response were measured by improvement of symptoms.

Results: A total of 404 children were included in this study with mean age group of 76.50 ± 36.62 months, and male-female ratio of 1.67:1. The most common presenting complaint was abdominal pain (66%), followed by anorexia (49%), vomiting (24%), nausea (17%), frequent defecation with small volume stool (17%), altered bowel habit (16%), failure to thrive (14%) and recurrent helminthiasis (12%). Interestingly, 2.5% children presented with persistent diarrhea.

Conclusion: Abdominal pain is the most common presentation of OC. When symptoms cannot be explained by other etiology, OC should be kept in mind.

背景:在我们的日常实践中,便秘是儿科人群的常见问题,也是门急诊就诊频繁的原因。但隐蔽性便秘(OC)仍然是最未解决的问题。目的:探讨儿童卵巢囊肿的临床特点。方法:这是一项前瞻性观察研究,于2022年1月至2024年12月在孟加拉国进行。它包括所有连续诊断为OC并进行相应治疗的儿童。在诊断前,通过适当的调查排除了出现症状的继发原因。每月随访4个月,以症状改善程度衡量治疗效果。结果:共纳入患儿404例,平均年龄76.50±36.62月,男女比例为1.67:1。最常见的症状是腹痛(66%),其次是厌食(49%)、呕吐(24%)、恶心(17%)、频繁排便且粪便体积小(17%)、排便习惯改变(16%)、发育不良(14%)和复发性寄生虫病(12%)。有趣的是,2.5%的儿童出现持续腹泻。结论:腹痛是腹膜炎最常见的表现。当症状不能由其他病因解释时,应考虑到卵巢癌。
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引用次数: 0
Monogenic defects in Russian children with autism spectrum disorders. 俄罗斯自闭症谱系障碍儿童的单基因缺陷。
Pub Date : 2025-12-09 DOI: 10.5409/wjcp.v14.i4.108733
Evgeny N Suspitsin, Kristina S Malysheva, Sergey A Laptiev, Olga S Sharonova, Anastasiya S Abuzova, Anastasiya A Kuznitsyna, Tatyana V Melashenko, Oksana V Efremova, Polina R Korzun, Jeyla O Binnatova, Yuliy A Gorgul, Maria V Syomina, Evgeny N Imyanitov
<p><strong>Background: </strong>Autism spectrum disorders (ASD) represent a substantial social problem affecting at least 1 in 100 children worldwide. These conditions are very often accompanied by intellectual disability (ID) and speech delay; thus, they can be considered within a clinical continuum of neurodevelopmental disorders. Given the high heterogeneity of ASD, the subjective nature of diagnostic criteria, and the presence of phenocopies, identifying genetic determinants of these disorders remains a challenge.</p><p><strong>Aim: </strong>To investigate the spectrum and frequency of rare genetic variants in genes with proven association with ASD in Russian children.</p><p><strong>Methods: </strong>110 patients from 106 families were recruited into the study (mean age at diagnosis 6 years; boy-to-girl ratio 3:1. Most of the patients (84%) demonstrated a combination of ASD with developmental delay (DD) or ID. Patients with syndromic features were subjected to the chromosomal microarray analysis. The remained children underwent clinical exome sequencing aimed at identifying presumably monogenic causes of ASD. The study focused on rare (minor allele frequency ≤ 0.001) variants affecting high-confidence ASD-associated genes.</p><p><strong>Results: </strong>Pathogenic copy number variations were detected in three (7%) of the patients examined. Clinical exome sequencing revealed pathogenic/likely pathogenic variants in 12 of 105 cases (11%), indicating the presence of monogenic syndromes with established clinical significance (Pitt-Hopkins syndrome, ZTTK syndrome, syndromic X-linked ID of Billuart type, Snijders-Blok-Campeau, Helsmoortel-van der Aa, Coffin-Siris, Clark-Baraitser, Keefstra syndromes, <i>etc.</i>). In addition, 27 patients (26%) had 37 rare variants of unknown clinical significance in <i>DSCAM</i>, <i>SHANK2</i>, <i>AUTS2</i>, <i>ADNP</i>, <i>ANKRD11</i>, <i>APBA2</i>, <i>ARID1B</i>, <i>ASTN2</i>, <i>ATRX</i>, <i>SCN1A</i>, <i>CHD2</i>, <i>DEAF1</i>, <i>EHMT1</i>, <i>GRIN2B</i>, <i>NBEA</i>, <i>NR4A2</i>, <i>TRIO</i>, <i>TRIP12</i>, <i>POGZ</i>, <i>EP300</i>, <i>FOXP1</i>, <i>PCDH19</i>, <i>GRIN2A</i>, <i>NCKAP1</i>, and <i>CHD8</i> genes. No specific variant was detected more than once in unrelated patients. Among the genes with rare variants found in 2 or more patients were <i>TRIP12</i> (<i>n</i> = 4), <i>AUTS2</i> (<i>n</i> = 3), <i>ARID1B</i> (<i>n</i> = 3), <i>PCDH19</i> (<i>n</i> = 3), <i>EP300</i> (<i>n</i> = 3), <i>TRIO</i> (<i>n</i> = 2), <i>ASTN2</i> (<i>n</i> = 2), <i>EHMT1</i> (<i>n</i> = 2), and <i>CHD2</i> (<i>n</i> = 2). Of note, 5 male ASD/DD patients from 3 unrelated families had <i>PCDH19</i> missense variants, confirming that at least some hemizygous males with non-mosaic <i>PCDH19</i> variants may present with neurobehavioral abnormalities. These variants did not cause epilepsy restricted to females in patients' mothers or sisters.</p><p><strong>Conclusion: </strong>These data confirm a tremendous diversity of
背景:自闭症谱系障碍(ASD)是一个严重的社会问题,全世界每100名儿童中至少有1人受到影响。这些情况往往伴随着智力障碍(ID)和语言迟缓;因此,它们可以被认为是神经发育障碍的临床连续体。鉴于自闭症谱系障碍的高度异质性、诊断标准的主观性以及表型的存在,确定这些疾病的遗传决定因素仍然是一个挑战。目的:探讨俄罗斯儿童ASD相关基因的罕见变异谱和频率。方法:来自106个家庭的110例患者(诊断时平均年龄6岁,男女比例3:1)纳入研究。大多数患者(84%)表现为ASD合并发育迟缓(DD)或发育迟缓(ID)。对具有综合征特征的患者进行染色体微阵列分析。剩下的儿童进行了临床外显子组测序,目的是确定可能的ASD单基因病因。该研究主要关注影响高置信度asd相关基因的罕见(小等位基因频率≤0.001)变异。结果:在3例(7%)患者中检测到致病性拷贝数变异。临床外显子组测序显示105例患者中有12例(11%)存在致病性/可能致病性变异,表明存在具有明确临床意义的单基因综合征(Pitt-Hopkins综合征、ZTTK综合征、Billuart型综合征x连锁ID、snijders - block - campeau、Helsmoortel-van der Aa、Coffin-Siris、Clark-Baraitser、Keefstra综合征等)。此外,27例(26%)患者在DSCAM、SHANK2、AUTS2、ADNP、ANKRD11、APBA2、ARID1B、ASTN2、ATRX、SCN1A、CHD2、DEAF1、EHMT1、GRIN2B、NBEA、NR4A2、TRIO、TRIP12、POGZ、EP300、FOXP1、PCDH19、GRIN2A、NCKAP1和CHD8基因中存在37种临床意义未知的罕见变异。在不相关的患者中没有检测到多于一次的特异性变异。在2例及以上患者中发现罕见变异的基因有TRIP12 (n = 4)、AUTS2 (n = 3)、ARID1B (n = 3)、PCDH19 (n = 3)、EP300 (n = 3)、TRIO (n = 2)、ASTN2 (n = 2)、EHMT1 (n = 2)和CHD2 (n = 2)。值得注意的是,来自3个不相关家族的5名男性ASD/DD患者存在PCDH19错义变异,这证实了至少一些具有非嵌合PCDH19变异的半合子男性可能存在神经行为异常。这些变异不会引起癫痫,仅限于患者母亲或姐妹中的女性。结论:这些数据证实了ASD的遗传原因存在巨大的多样性。临床外显子组测序可以作为全外显子组测序的合理替代方案。
{"title":"Monogenic defects in Russian children with autism spectrum disorders.","authors":"Evgeny N Suspitsin, Kristina S Malysheva, Sergey A Laptiev, Olga S Sharonova, Anastasiya S Abuzova, Anastasiya A Kuznitsyna, Tatyana V Melashenko, Oksana V Efremova, Polina R Korzun, Jeyla O Binnatova, Yuliy A Gorgul, Maria V Syomina, Evgeny N Imyanitov","doi":"10.5409/wjcp.v14.i4.108733","DOIUrl":"10.5409/wjcp.v14.i4.108733","url":null,"abstract":"&lt;p&gt;&lt;strong&gt;Background: &lt;/strong&gt;Autism spectrum disorders (ASD) represent a substantial social problem affecting at least 1 in 100 children worldwide. These conditions are very often accompanied by intellectual disability (ID) and speech delay; thus, they can be considered within a clinical continuum of neurodevelopmental disorders. Given the high heterogeneity of ASD, the subjective nature of diagnostic criteria, and the presence of phenocopies, identifying genetic determinants of these disorders remains a challenge.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Aim: &lt;/strong&gt;To investigate the spectrum and frequency of rare genetic variants in genes with proven association with ASD in Russian children.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Methods: &lt;/strong&gt;110 patients from 106 families were recruited into the study (mean age at diagnosis 6 years; boy-to-girl ratio 3:1. Most of the patients (84%) demonstrated a combination of ASD with developmental delay (DD) or ID. Patients with syndromic features were subjected to the chromosomal microarray analysis. The remained children underwent clinical exome sequencing aimed at identifying presumably monogenic causes of ASD. The study focused on rare (minor allele frequency ≤ 0.001) variants affecting high-confidence ASD-associated genes.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Results: &lt;/strong&gt;Pathogenic copy number variations were detected in three (7%) of the patients examined. Clinical exome sequencing revealed pathogenic/likely pathogenic variants in 12 of 105 cases (11%), indicating the presence of monogenic syndromes with established clinical significance (Pitt-Hopkins syndrome, ZTTK syndrome, syndromic X-linked ID of Billuart type, Snijders-Blok-Campeau, Helsmoortel-van der Aa, Coffin-Siris, Clark-Baraitser, Keefstra syndromes, &lt;i&gt;etc.&lt;/i&gt;). In addition, 27 patients (26%) had 37 rare variants of unknown clinical significance in &lt;i&gt;DSCAM&lt;/i&gt;, &lt;i&gt;SHANK2&lt;/i&gt;, &lt;i&gt;AUTS2&lt;/i&gt;, &lt;i&gt;ADNP&lt;/i&gt;, &lt;i&gt;ANKRD11&lt;/i&gt;, &lt;i&gt;APBA2&lt;/i&gt;, &lt;i&gt;ARID1B&lt;/i&gt;, &lt;i&gt;ASTN2&lt;/i&gt;, &lt;i&gt;ATRX&lt;/i&gt;, &lt;i&gt;SCN1A&lt;/i&gt;, &lt;i&gt;CHD2&lt;/i&gt;, &lt;i&gt;DEAF1&lt;/i&gt;, &lt;i&gt;EHMT1&lt;/i&gt;, &lt;i&gt;GRIN2B&lt;/i&gt;, &lt;i&gt;NBEA&lt;/i&gt;, &lt;i&gt;NR4A2&lt;/i&gt;, &lt;i&gt;TRIO&lt;/i&gt;, &lt;i&gt;TRIP12&lt;/i&gt;, &lt;i&gt;POGZ&lt;/i&gt;, &lt;i&gt;EP300&lt;/i&gt;, &lt;i&gt;FOXP1&lt;/i&gt;, &lt;i&gt;PCDH19&lt;/i&gt;, &lt;i&gt;GRIN2A&lt;/i&gt;, &lt;i&gt;NCKAP1&lt;/i&gt;, and &lt;i&gt;CHD8&lt;/i&gt; genes. No specific variant was detected more than once in unrelated patients. Among the genes with rare variants found in 2 or more patients were &lt;i&gt;TRIP12&lt;/i&gt; (&lt;i&gt;n&lt;/i&gt; = 4), &lt;i&gt;AUTS2&lt;/i&gt; (&lt;i&gt;n&lt;/i&gt; = 3), &lt;i&gt;ARID1B&lt;/i&gt; (&lt;i&gt;n&lt;/i&gt; = 3), &lt;i&gt;PCDH19&lt;/i&gt; (&lt;i&gt;n&lt;/i&gt; = 3), &lt;i&gt;EP300&lt;/i&gt; (&lt;i&gt;n&lt;/i&gt; = 3), &lt;i&gt;TRIO&lt;/i&gt; (&lt;i&gt;n&lt;/i&gt; = 2), &lt;i&gt;ASTN2&lt;/i&gt; (&lt;i&gt;n&lt;/i&gt; = 2), &lt;i&gt;EHMT1&lt;/i&gt; (&lt;i&gt;n&lt;/i&gt; = 2), and &lt;i&gt;CHD2&lt;/i&gt; (&lt;i&gt;n&lt;/i&gt; = 2). Of note, 5 male ASD/DD patients from 3 unrelated families had &lt;i&gt;PCDH19&lt;/i&gt; missense variants, confirming that at least some hemizygous males with non-mosaic &lt;i&gt;PCDH19&lt;/i&gt; variants may present with neurobehavioral abnormalities. These variants did not cause epilepsy restricted to females in patients' mothers or sisters.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Conclusion: &lt;/strong&gt;These data confirm a tremendous diversity of ","PeriodicalId":75338,"journal":{"name":"World journal of clinical pediatrics","volume":"14 4","pages":"108733"},"PeriodicalIF":0.0,"publicationDate":"2025-12-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12620798/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145552258","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Quality of life in children with chronic pancreatitis: An overlooked challenge. 慢性胰腺炎儿童的生活质量:一个被忽视的挑战。
Pub Date : 2025-12-09 DOI: 10.5409/wjcp.v14.i4.109615
Ankit Agrawal, Arghya Samanta

Chronic pancreatitis (CP) is no longer considered a disease of adults alone; it is increasingly being recognized in children as well. It is a chronic inflammatory condition of the pancreas that can lead to exocrine and endocrine insufficiency over time. The clinical aspects and medical management of pediatric CP are often discussed; however, its impact on the quality of life (QOL) remains largely unaddressed in routine clinical care. The review focus on physical, emotional, educational, and social challenges experienced by children with CP and their families. Pain-related disability, frequent hospitalizations, and the risk of developing exocrine and endocrine insufficiency significantly affect daily functioning and mental well-being. Therefore, improving QOL in children with CP requires a multidisciplinary care strategy, including effective pain management, nutritional optimization, and psychological support.

慢性胰腺炎(CP)不再被认为是成人独有的疾病;儿童也越来越多地认识到这一点。它是胰腺的一种慢性炎症,随着时间的推移会导致外分泌和内分泌不足。儿童CP的临床方面和医疗管理经常被讨论;然而,其对生活质量(QOL)的影响在常规临床护理中仍未得到解决。本综述的重点是CP儿童及其家庭所经历的身体、情感、教育和社会挑战。与疼痛相关的残疾、频繁住院以及发展为外分泌和内分泌功能不全的风险显著影响日常功能和心理健康。因此,改善CP患儿的生活质量需要多学科的护理策略,包括有效的疼痛管理、营养优化和心理支持。
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引用次数: 0
Diabetes in adolescents without obesity in India: An underrecognized phenotype. 印度无肥胖青少年的糖尿病:一种未被充分认识的表型。
Pub Date : 2025-12-09 DOI: 10.5409/wjcp.v14.i4.110032
Rashi Agrawal, Akhila Bhandarkar, Nitin Kapoor

Adolescent type 2 diabetes mellitus (T2DM) is on the rise in India and is commonly attributed to co-existence of overweight and obesity in adolescents. In this line, a study by Maheshwari et al titled 'Prevalence of obesity, determinants, and its association with hyperglycaemia among community dwelling older adolescents in India' concluded that overweight, obesity, socioeconomic factors and higher education status were responsible for hyperglycemia in adolescents aged 15-19 years in India. We highlight that there is a significant prevalence of T2DM even in normal body mass index (BMI) and below normal BMI subjects, as mentioned in their study. There is a high prevalence of normal weight obesity in Indian adolescents which often gets missed due to a large population with normal BMI in the country. In this letter, we analyze the importance of measurement of central adiposity beyond routine BMI measurements.

青少年2型糖尿病(T2DM)在印度呈上升趋势,通常归因于青少年超重和肥胖的共存。在这方面,Maheshwari等人的一项题为“印度社区居住的大龄青少年中肥胖的患病率、决定因素及其与高血糖的关系”的研究得出结论,超重、肥胖、社会经济因素和高等教育状况是印度15-19岁青少年高血糖的原因。我们强调,正如他们的研究中提到的,即使在正常体重指数(BMI)和低于正常体重指数的受试者中,T2DM也有显著的患病率。印度青少年中正常体重肥胖的患病率很高,但由于该国有大量正常体重指数的人口,这一比例经常被忽视。在这封信中,我们分析了测量中心性肥胖在常规BMI测量之外的重要性。
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引用次数: 0
Towards improved neonatal care: Developing reference intervals for biochemical parameters in umbilical cord blood: An Indian study. 改善新生儿护理:发展脐带血生化参数的参考区间:一项印度研究。
Pub Date : 2025-12-09 DOI: 10.5409/wjcp.v14.i4.107181
Keyur Sabnis, Swati Ghanghurde, Akash Shukla, Dhriti Sukheja, Mohit Vijay Rojekar

Background: The reference ranges for biochemical parameters can fluctuate due to factors like altitude, age, gender, and socioeconomic conditions. These values are crucial for interpreting laboratory data and guide clinical treatment decisions. Currently, there is no established set of reference intervals for cord blood biochemical parameters of newborns in India, particularly in Mumbai.

Aim: To create cord blood biochemical parameters reference intervals specifically for Mumbai, India.

Methods: A cross-sectional study was conducted in an Indian tertiary care hospital. This study focused on healthy newborns with normal birth weight, born to pregnant mothers without health issues. Cord blood samples, approximately 2-3 mL in volume, were collected from 210 term neonates. These samples were divided into fluoride (glucose) and clot activator (serum) tubes and were subsequently analyzed in the institute's biochemical laboratory. The data obtained from the analysis was then subjected to statistical analysis. The result of the Shapiro-Wilk test suggested non-normality in the data distribution. Consequently, non-parametric statistics were utilized for analysis. The Mann-Whitney U test was utilized to compare parameter distributions among different factors, including the infant's sex, delivery method, maternal age, and obstetric history. A significance level of P < 0.05 was considered to indicate statistical significance.

Results: The following represent the median figures and central 95 percentile reference intervals for biochemical parameters in umbilical cord blood of newborns: Serum direct bilirubin = (0.1-0.55) mg/dL, indirect bilirubin = (0.64-2.26) mg/dL, total bilirubin = (0.62-3.14) mg/dL, creatinine = (0.27-0.76) mg/dL, sodium = (128.19-143.26) mmol/L, chloride = (100.19-111.68) mmol/L, potassium = (1.62-9.98) mmol/L and plasma glucose = (24.75-94.23) mg/dL. Statistically significant differences were observed in serum sodium, potassium, and plasma glucose levels when comparing delivery modes.

Conclusion: This is the pioneering study in which first time, the biochemical reference intervals in cord blood for newborns are established in western India. The values are applicable for newborns from this area. Larger study throughout the country is required.

背景:生化指标参考范围会因海拔、年龄、性别、社会经济条件等因素而波动。这些值对于解释实验室数据和指导临床治疗决策至关重要。目前,在印度,特别是在孟买,没有建立一套新生儿脐带血生化参数的参考区间。目的:为印度孟买地区建立脐带血生化参数参考区间。方法:在印度一家三级医院进行横断面研究。这项研究的重点是没有健康问题的孕妇所生的体重正常的健康新生儿。从210名足月新生儿中采集脐带血样本,体积约为2-3 mL。这些样品被分成氟化物(葡萄糖)和凝块激活剂(血清)管,随后在研究所的生化实验室进行分析。从分析中获得的数据然后进行统计分析。夏皮罗-威尔克检验结果表明数据分布存在非正态性。因此,使用非参数统计进行分析。采用Mann-Whitney U检验比较婴儿性别、分娩方式、产妇年龄、产科史等不同因素的参数分布。以P < 0.05为显著性水平。结果:新生儿脐带血生化指标的中位数和中位95百分位参考区间为:血清直接胆红素= (0.1 ~ 0.55)mg/dL,间接胆红素= (0.64 ~ 2.26)mg/dL,总胆红素= (0.62 ~ 3.14)mg/dL,肌酐= (0.27 ~ 0.76)mg/dL,钠= (128.19 ~ 143.26)mmol/L,氯= (100.19 ~ 111.68)mmol/L,钾= (1.62 ~ 9.98)mmol/L,血浆葡萄糖= (24.75 ~ 94.23)mg/dL。在比较给药方式时,观察到血清钠、钾和血浆葡萄糖水平有统计学意义的差异。结论:这是印度西部首次建立新生儿脐带血生化参考区间的开创性研究。这些值适用于该地区的新生儿。需要在全国范围内进行更大规模的研究。
{"title":"Towards improved neonatal care: Developing reference intervals for biochemical parameters in umbilical cord blood: An Indian study.","authors":"Keyur Sabnis, Swati Ghanghurde, Akash Shukla, Dhriti Sukheja, Mohit Vijay Rojekar","doi":"10.5409/wjcp.v14.i4.107181","DOIUrl":"10.5409/wjcp.v14.i4.107181","url":null,"abstract":"<p><strong>Background: </strong>The reference ranges for biochemical parameters can fluctuate due to factors like altitude, age, gender, and socioeconomic conditions. These values are crucial for interpreting laboratory data and guide clinical treatment decisions. Currently, there is no established set of reference intervals for cord blood biochemical parameters of newborns in India, particularly in Mumbai.</p><p><strong>Aim: </strong>To create cord blood biochemical parameters reference intervals specifically for Mumbai, India.</p><p><strong>Methods: </strong>A cross-sectional study was conducted in an Indian tertiary care hospital. This study focused on healthy newborns with normal birth weight, born to pregnant mothers without health issues. Cord blood samples, approximately 2-3 mL in volume, were collected from 210 term neonates. These samples were divided into fluoride (glucose) and clot activator (serum) tubes and were subsequently analyzed in the institute's biochemical laboratory. The data obtained from the analysis was then subjected to statistical analysis. The result of the Shapiro-Wilk test suggested non-normality in the data distribution. Consequently, non-parametric statistics were utilized for analysis. The Mann-Whitney <i>U</i> test was utilized to compare parameter distributions among different factors, including the infant's sex, delivery method, maternal age, and obstetric history. A significance level of <i>P</i> < 0.05 was considered to indicate statistical significance.</p><p><strong>Results: </strong>The following represent the median figures and central 95 percentile reference intervals for biochemical parameters in umbilical cord blood of newborns: Serum direct bilirubin = (0.1-0.55) mg/dL, indirect bilirubin = (0.64-2.26) mg/dL, total bilirubin = (0.62-3.14) mg/dL, creatinine = (0.27-0.76) mg/dL, sodium = (128.19-143.26) mmol/L, chloride = (100.19-111.68) mmol/L, potassium = (1.62-9.98) mmol/L and plasma glucose = (24.75-94.23) mg/dL. Statistically significant differences were observed in serum sodium, potassium, and plasma glucose levels when comparing delivery modes.</p><p><strong>Conclusion: </strong>This is the pioneering study in which first time, the biochemical reference intervals in cord blood for newborns are established in western India. The values are applicable for newborns from this area. Larger study throughout the country is required.</p>","PeriodicalId":75338,"journal":{"name":"World journal of clinical pediatrics","volume":"14 4","pages":"107181"},"PeriodicalIF":0.0,"publicationDate":"2025-12-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12620816/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145552281","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Steroid response and outcomes in childhood nephrotic syndrome: A multicenter, cross-sectional study from Jordan. 儿童肾病综合征的类固醇反应和结局:一项来自约旦的多中心横断面研究。
Pub Date : 2025-12-09 DOI: 10.5409/wjcp.v14.i4.109671
Salma A Ajarmeh, Kamal Akl, Muna Al Shawabkeh, Jumana Al Baramki

Background: Childhood nephrotic syndrome (NS) outcomes vary widely based on steroid responsiveness and complications.

Aim: To evaluate steroid response, outcomes, and the use of steroid-sparing medications in children with nephrotic syndrome in Jordan.

Methods: This retrospective study evaluated the demographics and outcomes of 122 children aged 1-18 years with NS between 2011 and 2021 across three centers in Jordan. The outcomes assessed included steroid sensitivity rates, dependence, frequent relapses, complications [chronic kidney disease (CKD), end-stage kidney disease (ESKD)], infections, and need for steroid-sparing treatment.

Results: Of 64% were boys; median age of disease onset was 4 years. Steroid-sensitive and steroid-resistant NS (SRNS) were observed in 81.1% and 18.9% of patients, respectively; 28.7% and 9% had steroid-dependent and frequently relapsing NS, respectively. Kidney biopsies were conducted in 46.7%, the most common finding was minimal change disease in 56.1%; 82.6% of biopsied SRNS cases showed focal segmental glomerulosclerosis. The median time to first relapse was 9 months. 41.8% of patients required steroid-sparing medications, with cyclosporine and mycophenolate mofetil being the most frequently used. Despite these treatments, relapse occurred in 11.5% of cases. Infections, primarily urinary tract infections, affected 24.6% of patients, 7.4% progressed to high-grade CKD, and 6.6% required dialysis. SRNS was significantly associated with hematuria, hypertension, and ESKD.

Conclusion: Most patients were steroid sensitive, with minimal change being the most common. Focal segmental glomerulosclerosis was the predominant histopathology in the steroid-resistant cases. SRNS patients had worse outcomes, with more infections, CKD, and ESKD.

背景:儿童肾病综合征(NS)的结局因类固醇反应性和并发症而有很大差异。目的:评价约旦儿童肾病综合征的类固醇反应、结局和类固醇保留药物的使用。方法:本回顾性研究评估了2011年至2021年间约旦三个中心122名1-18岁NS患儿的人口统计学和结局。评估的结果包括类固醇敏感性、依赖性、频繁复发、并发症[慢性肾脏疾病(CKD)、终末期肾脏疾病(ESKD)]、感染以及是否需要类固醇治疗。结果:男孩占64%;发病的中位年龄为4岁。81.1%和18.9%的患者出现激素敏感型和激素耐药型NS (SRNS);28.7%和9%分别为类固醇依赖性和频繁复发的NS。肾活检占46.7%,最常见的发现是微小病变(56.1%);82.6%的SRNS活检病例显示局灶性节段性肾小球硬化。首次复发的中位时间为9个月。41.8%的患者需要保留类固醇的药物,环孢素和霉酚酸酯是最常用的。尽管进行了这些治疗,仍有11.5%的病例复发。感染,主要是尿路感染,影响了24.6%的患者,7.4%进展为高级别CKD, 6.6%需要透析。SRNS与血尿、高血压和ESKD显著相关。结论:大多数患者对类固醇敏感,以微小变化最为常见。局灶节段性肾小球硬化是类固醇抵抗病例的主要组织病理学。SRNS患者的预后较差,感染、CKD和ESKD发生率更高。
{"title":"Steroid response and outcomes in childhood nephrotic syndrome: A multicenter, cross-sectional study from Jordan.","authors":"Salma A Ajarmeh, Kamal Akl, Muna Al Shawabkeh, Jumana Al Baramki","doi":"10.5409/wjcp.v14.i4.109671","DOIUrl":"10.5409/wjcp.v14.i4.109671","url":null,"abstract":"<p><strong>Background: </strong>Childhood nephrotic syndrome (NS) outcomes vary widely based on steroid responsiveness and complications.</p><p><strong>Aim: </strong>To evaluate steroid response, outcomes, and the use of steroid-sparing medications in children with nephrotic syndrome in Jordan.</p><p><strong>Methods: </strong>This retrospective study evaluated the demographics and outcomes of 122 children aged 1-18 years with NS between 2011 and 2021 across three centers in Jordan. The outcomes assessed included steroid sensitivity rates, dependence, frequent relapses, complications [chronic kidney disease (CKD), end-stage kidney disease (ESKD)], infections, and need for steroid-sparing treatment.</p><p><strong>Results: </strong>Of 64% were boys; median age of disease onset was 4 years. Steroid-sensitive and steroid-resistant NS (SRNS) were observed in 81.1% and 18.9% of patients, respectively; 28.7% and 9% had steroid-dependent and frequently relapsing NS, respectively. Kidney biopsies were conducted in 46.7%, the most common finding was minimal change disease in 56.1%; 82.6% of biopsied SRNS cases showed focal segmental glomerulosclerosis. The median time to first relapse was 9 months. 41.8% of patients required steroid-sparing medications, with cyclosporine and mycophenolate mofetil being the most frequently used. Despite these treatments, relapse occurred in 11.5% of cases. Infections, primarily urinary tract infections, affected 24.6% of patients, 7.4% progressed to high-grade CKD, and 6.6% required dialysis. SRNS was significantly associated with hematuria, hypertension, and ESKD.</p><p><strong>Conclusion: </strong>Most patients were steroid sensitive, with minimal change being the most common. Focal segmental glomerulosclerosis was the predominant histopathology in the steroid-resistant cases. SRNS patients had worse outcomes, with more infections, CKD, and ESKD.</p>","PeriodicalId":75338,"journal":{"name":"World journal of clinical pediatrics","volume":"14 4","pages":"109671"},"PeriodicalIF":0.0,"publicationDate":"2025-12-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12620775/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145552313","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Long-term consequences of unintended pregnancy: Impacts on early childhood growth and development in a multicenter study. 意外怀孕的长期后果:多中心研究对儿童早期生长发育的影响
Pub Date : 2025-12-09 DOI: 10.5409/wjcp.v14.i4.107346
Linda Yanti, Surtiningsih, Fauziah Hanum Nur Ardiyani, Ni Nyoman Ayu Desy Sekarini, Dwi Susanti, Mustaan, Murniati, Supriyadi, Agus Santosa

Background: Unintended pregnancy occurs when an individual or couple conceives without planning or desire, which can potentially affect a child's physical, mental, and social well-being. This can then lead to long-term socioeconomic challenges for families and communities. Although its impact on child growth and development is a pressing concern, research remains limited particularly in multicenter settings.

Aim: To examine the long-term consequences of unintended pregnancy on the critical years of early childhood growth and development.

Methods: This analytical observational study employed a case-control design and was conducted in research centers across Indonesia, encompassing those located in Central Java, Lampung, Bali, and West Nusa Tenggara. A total of 700 children aged ≤ 5 years with histories of intended or unintended pregnancies participated. Data collection involved structured interviews and direct anthropometric and developmental assessments. Data analyses were conducted using multivariate statistics and partial least squares structural equation modeling.

Results: Unintended pregnancy was found to have a statistically significant effect on both child growth (t = 8.178; P < 0.001) and child development (t = 25.688; P < 0.001). Key growth problems identified included underweight, undernutrition, abnormal head circumference, and stunting. Developmental challenges prominently associated with unintended pregnancy included behavioral and emotional disorders, autism spectrum disorder, attention-deficit/hyperactivity disorder, social and motor skill deficits, as well as visual and hearing impairments.

Conclusion: Unintended pregnancy significantly affects child growth and development, underscoring the need for early intervention, quality prenatal care, and strengthened family planning policies.

背景:意外怀孕是指个人或夫妇在没有计划或意愿的情况下怀孕,这可能会影响孩子的身体、精神和社会福祉。这可能会给家庭和社区带来长期的社会经济挑战。虽然它对儿童生长发育的影响是一个紧迫的问题,但研究仍然有限,特别是在多中心环境中。目的:研究意外怀孕对儿童早期生长发育的长期影响。方法:本分析观察性研究采用病例对照设计,在印度尼西亚各地的研究中心进行,包括位于中爪哇、楠榜、巴厘岛和西努沙登加拉的研究中心。共有700名年龄≤5岁且有有意或意外怀孕史的儿童参与。数据收集包括结构化访谈和直接人体测量和发育评估。数据分析采用多元统计和偏最小二乘结构方程模型。结果:意外妊娠对儿童生长(t = 8.178, P < 0.001)和发育(t = 25.688, P < 0.001)均有统计学意义。确定的主要生长问题包括体重不足、营养不良、头围异常和发育迟缓。与意外怀孕显著相关的发育挑战包括行为和情绪障碍、自闭症谱系障碍、注意力缺陷/多动障碍、社交和运动技能缺陷,以及视觉和听力障碍。结论:意外妊娠严重影响儿童生长发育,需要早期干预、优质产前护理和强化计划生育政策。
{"title":"Long-term consequences of unintended pregnancy: Impacts on early childhood growth and development in a multicenter study.","authors":"Linda Yanti, Surtiningsih, Fauziah Hanum Nur Ardiyani, Ni Nyoman Ayu Desy Sekarini, Dwi Susanti, Mustaan, Murniati, Supriyadi, Agus Santosa","doi":"10.5409/wjcp.v14.i4.107346","DOIUrl":"10.5409/wjcp.v14.i4.107346","url":null,"abstract":"<p><strong>Background: </strong>Unintended pregnancy occurs when an individual or couple conceives without planning or desire, which can potentially affect a child's physical, mental, and social well-being. This can then lead to long-term socioeconomic challenges for families and communities. Although its impact on child growth and development is a pressing concern, research remains limited particularly in multicenter settings.</p><p><strong>Aim: </strong>To examine the long-term consequences of unintended pregnancy on the critical years of early childhood growth and development.</p><p><strong>Methods: </strong>This analytical observational study employed a case-control design and was conducted in research centers across Indonesia, encompassing those located in Central Java, Lampung, Bali, and West Nusa Tenggara. A total of 700 children aged ≤ 5 years with histories of intended or unintended pregnancies participated. Data collection involved structured interviews and direct anthropometric and developmental assessments. Data analyses were conducted using multivariate statistics and partial least squares structural equation modeling.</p><p><strong>Results: </strong>Unintended pregnancy was found to have a statistically significant effect on both child growth (<i>t</i> = 8.178; <i>P</i> < 0.001) and child development (<i>t</i> = 25.688; <i>P</i> < 0.001). Key growth problems identified included underweight, undernutrition, abnormal head circumference, and stunting. Developmental challenges prominently associated with unintended pregnancy included behavioral and emotional disorders, autism spectrum disorder, attention-deficit/hyperactivity disorder, social and motor skill deficits, as well as visual and hearing impairments.</p><p><strong>Conclusion: </strong>Unintended pregnancy significantly affects child growth and development, underscoring the need for early intervention, quality prenatal care, and strengthened family planning policies.</p>","PeriodicalId":75338,"journal":{"name":"World journal of clinical pediatrics","volume":"14 4","pages":"107346"},"PeriodicalIF":0.0,"publicationDate":"2025-12-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12620778/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145552183","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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World journal of clinical pediatrics
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