{"title":"血清脂肪因子是监测中低收入国家儿童急性淋巴细胞白血病幸存者代谢综合征的生物标记物","authors":"Gargi Das, Kritika Setlur, Manisha Jana, Lakshmy Ramakrishnan, Vandana Jain, Jagdish Prasad Meena, Aditya Kumar Gupta, Sada Nand Dwivedi, Rachna Seth","doi":"10.1080/01635581.2023.2301139","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Serum adipokines (leptin and adiponectin) are dysregulated before the onset of metabolic syndrome and hence may be useful biomarkers for screening of cardiometabolic late effects in childhood Acute Lymphoblastic Leukemia (cALL) survivors.</p><p><strong>Methods: </strong>We compared serum adipokine levels between 40 cALL survivors (aged 10-18 years, >2 years from treatment completion) with similar controls. A multivariable logistic regression analysis was then done to assess the association of metabolic syndrome in cALL survivors with variables including adipokines and other metabolic parameters, demographic and treatment details, and Dual-energy X-ray absorptiometry scan-derived variables.</p><p><strong>Results: </strong>Compared to controls, cALL survivors had a higher prevalence of metabolic syndrome (8/40 vs. 2/40, <i>P</i> = .044) and central obesity (11/40 vs. 4/40, <i>P</i> = 0.042). Median Serum Leptin (7.39 vs. 4.23 ng/ml, <i>P</i> = 0.207) levels and derived Leptin-Adiponectin Ratio (1.44 vs. 0.80, <i>P</i> = 0.598), were higher but not statistically different in our survivors compared to controls; Adiponectin levels were similar (6.07 vs. 5.01 µg/ml, <i>P</i> = 0.283). In the cALL survivors, overweight/obesity (odds ratio [OR] 21.9, <i>P</i> = 0.020) or higher Leptin levels (OR 1.11, <i>P</i> = 0.047), were independently associated with metabolic syndrome.</p><p><strong>Conclusions: </strong>Serum Leptin, independently predictive of metabolic syndrome in our cALL survivors, may be tested in larger studies to assess its utility in surveillance and initiation of early preventive measures.</p>","PeriodicalId":54701,"journal":{"name":"Nutrition and Cancer-An International Journal","volume":" ","pages":"262-270"},"PeriodicalIF":2.0000,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Serum Adipokines as Biomarkers for Surveillance of Metabolic Syndrome in Childhood Acute Lymphoblastic Leukemia Survivors in Low Middle-Income Countries.\",\"authors\":\"Gargi Das, Kritika Setlur, Manisha Jana, Lakshmy Ramakrishnan, Vandana Jain, Jagdish Prasad Meena, Aditya Kumar Gupta, Sada Nand Dwivedi, Rachna Seth\",\"doi\":\"10.1080/01635581.2023.2301139\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>Serum adipokines (leptin and adiponectin) are dysregulated before the onset of metabolic syndrome and hence may be useful biomarkers for screening of cardiometabolic late effects in childhood Acute Lymphoblastic Leukemia (cALL) survivors.</p><p><strong>Methods: </strong>We compared serum adipokine levels between 40 cALL survivors (aged 10-18 years, >2 years from treatment completion) with similar controls. A multivariable logistic regression analysis was then done to assess the association of metabolic syndrome in cALL survivors with variables including adipokines and other metabolic parameters, demographic and treatment details, and Dual-energy X-ray absorptiometry scan-derived variables.</p><p><strong>Results: </strong>Compared to controls, cALL survivors had a higher prevalence of metabolic syndrome (8/40 vs. 2/40, <i>P</i> = .044) and central obesity (11/40 vs. 4/40, <i>P</i> = 0.042). Median Serum Leptin (7.39 vs. 4.23 ng/ml, <i>P</i> = 0.207) levels and derived Leptin-Adiponectin Ratio (1.44 vs. 0.80, <i>P</i> = 0.598), were higher but not statistically different in our survivors compared to controls; Adiponectin levels were similar (6.07 vs. 5.01 µg/ml, <i>P</i> = 0.283). In the cALL survivors, overweight/obesity (odds ratio [OR] 21.9, <i>P</i> = 0.020) or higher Leptin levels (OR 1.11, <i>P</i> = 0.047), were independently associated with metabolic syndrome.</p><p><strong>Conclusions: </strong>Serum Leptin, independently predictive of metabolic syndrome in our cALL survivors, may be tested in larger studies to assess its utility in surveillance and initiation of early preventive measures.</p>\",\"PeriodicalId\":54701,\"journal\":{\"name\":\"Nutrition and Cancer-An International Journal\",\"volume\":\" \",\"pages\":\"262-270\"},\"PeriodicalIF\":2.0000,\"publicationDate\":\"2024-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Nutrition and Cancer-An International Journal\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1080/01635581.2023.2301139\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2024/2/1 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q3\",\"JCRName\":\"NUTRITION & DIETETICS\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Nutrition and Cancer-An International Journal","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1080/01635581.2023.2301139","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/2/1 0:00:00","PubModel":"Epub","JCR":"Q3","JCRName":"NUTRITION & DIETETICS","Score":null,"Total":0}
引用次数: 0
摘要
背景:血清脂肪因子(瘦素和脂肪连蛋白)在代谢综合征发病前就会失调,因此可能是筛查儿童急性淋巴细胞白血病(cALL)幸存者心脏代谢晚期效应的有用生物标志物:我们比较了 40 名儿童急性淋巴细胞白血病(cALL)幸存者(年龄在 10-18 岁之间,距离治疗结束时间超过 2 年)与相似对照组的血清脂肪因子水平。然后进行了多变量逻辑回归分析,以评估 cALL 存活者的代谢综合征与包括脂肪因子和其他代谢参数、人口统计学和治疗细节以及双能 X 射线吸收测量扫描衍生变量在内的变量之间的关联:结果:与对照组相比,CALL 幸存者代谢综合征(8/40 vs. 2/40,P = .044)和中心性肥胖(11/40 vs. 4/40,P = 0.042)的发病率更高。与对照组相比,幸存者的血清瘦素中位数(7.39 vs. 4.23 ng/ml,P = 0.207)水平和衍生的瘦素-脂联素比率(1.44 vs. 0.80,P = 0.598)较高,但无统计学差异;脂联素水平相似(6.07 vs. 5.01 µg/ml,P = 0.283)。在 cALL 幸存者中,超重/肥胖(几率比 [OR] 21.9,P = 0.020)或较高的瘦素水平(OR 1.11,P = 0.047)与代谢综合征独立相关:结论:血清瘦素可独立预测 CALL 幸存者的代谢综合征,可在更大规模的研究中对其进行测试,以评估其在监测和启动早期预防措施方面的效用。
Serum Adipokines as Biomarkers for Surveillance of Metabolic Syndrome in Childhood Acute Lymphoblastic Leukemia Survivors in Low Middle-Income Countries.
Background: Serum adipokines (leptin and adiponectin) are dysregulated before the onset of metabolic syndrome and hence may be useful biomarkers for screening of cardiometabolic late effects in childhood Acute Lymphoblastic Leukemia (cALL) survivors.
Methods: We compared serum adipokine levels between 40 cALL survivors (aged 10-18 years, >2 years from treatment completion) with similar controls. A multivariable logistic regression analysis was then done to assess the association of metabolic syndrome in cALL survivors with variables including adipokines and other metabolic parameters, demographic and treatment details, and Dual-energy X-ray absorptiometry scan-derived variables.
Results: Compared to controls, cALL survivors had a higher prevalence of metabolic syndrome (8/40 vs. 2/40, P = .044) and central obesity (11/40 vs. 4/40, P = 0.042). Median Serum Leptin (7.39 vs. 4.23 ng/ml, P = 0.207) levels and derived Leptin-Adiponectin Ratio (1.44 vs. 0.80, P = 0.598), were higher but not statistically different in our survivors compared to controls; Adiponectin levels were similar (6.07 vs. 5.01 µg/ml, P = 0.283). In the cALL survivors, overweight/obesity (odds ratio [OR] 21.9, P = 0.020) or higher Leptin levels (OR 1.11, P = 0.047), were independently associated with metabolic syndrome.
Conclusions: Serum Leptin, independently predictive of metabolic syndrome in our cALL survivors, may be tested in larger studies to assess its utility in surveillance and initiation of early preventive measures.
期刊介绍:
This timely publication reports and reviews current findings on the effects of nutrition on the etiology, therapy, and prevention of cancer. Etiological issues include clinical and experimental research in nutrition, carcinogenesis, epidemiology, biochemistry, and molecular biology. Coverage of therapy focuses on research in clinical nutrition and oncology, dietetics, and bioengineering. Prevention approaches include public health recommendations, preventative medicine, behavior modification, education, functional foods, and agricultural and food production policies.