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亚生育力作为营养、内分泌、免疫和心脏代谢失调的重叠——一项聚焦于亚生育夫妇生化内表型的研究

Subfertility as Overlapping of Nutritional, Endocrine, Immune, and Cardiometabolic Dysregulations-A Study Focused on Biochemical Endophenotypes of Subfertile Couples.

作者信息

Wasilewski Tadeusz, Wasilewska Jolanta, Łukaszewicz-Zając Marta, Mroczko Barbara

机构信息

Centre for Restorative Procreative Medicine, Napromedica, 15-741 Bialystok, Poland.

Centre for Paediatrics, Allergology, Psychodietetics, and Treatment of Children Diagnosed with Autism, IPM, 15-404 Bialystok, Poland.

出版信息

J Clin Med. 2023 Sep 21;12(18):6094. doi: 10.3390/jcm12186094.

Abstract

Subfertility is a global health issue, and as many as 30% of cases are attributed to unexplained reasons. A hypercaloric, high-fat diet stimulates the expansion of pro-inflammatory gut microbiota with a consequent rise in circulating lipopolysaccharides. Adverse gut microbiota remodeling can exacerbate insulin resistance, while sex and thyroid hormones may influence the variability in gut microbiota. This cross-sectional study included 150 participants and was designed to determine a biochemical, nutritional-related pattern that may distinguish subfertile from fertile individuals and couples. A panel of 28 biomarkers was assessed. Four biochemical phenotypes of unexplained subfertility were found, including two metabolic and two immune, when assessed using binary logistic regression models. Two phenotypes were distinguished in women: cardio-metabolic with atherogenic dyslipidemia (HDL-cholesterol: OR = 10.9; < 0.05) and autoimmune thyroid disorder (anti-thyroid-peroxidase: OR = 5.5; < 0.05) and two in men: hepato-metabolic with elevated liver injury enzymes (HOMA-IR: OR = 6.1; < 0.05) and immune type-2 response (IgE: OR = 6.4; < 0.05). The chances of a couple's subfertility rose with the number of laboratory components of metabolic syndrome in the couple (OR = 1.7; < 0.05) and if at least one partner had an elevated total IgE level (>100 kU/L) (OR = 6.5; < 0.05). This study found that unexplained subfertility may be accompanied by mutually overlapping immune and metabolic dysregulations in individuals and couples. We propose one-time laboratory diagnostics taking into account the lipid profile, insulin resistance, anti-thyroid-peroxidase, and total IgE in both males and females with unexplained subfertility. This may allow for a one-time assessment of targeted medical and nutritional interventions and help optimize patients' health. The gut-organ axes related to subfertility are discussed in the context of the obtained results.

摘要

亚生育力是一个全球性的健康问题,多达30%的病例归因于不明原因。高热量、高脂肪饮食会刺激促炎性肠道微生物群的扩张,从而导致循环中的脂多糖增加。不良的肠道微生物群重塑会加剧胰岛素抵抗,而性激素和甲状腺激素可能会影响肠道微生物群的变异性。这项横断面研究纳入了150名参与者,旨在确定一种可能区分亚生育力个体和夫妇与生育力正常个体和夫妇的生化、营养相关模式。评估了一组28种生物标志物。在使用二元逻辑回归模型进行评估时,发现了四种不明原因亚生育力的生化表型,包括两种代谢型和两种免疫型。在女性中区分出两种表型:具有致动脉粥样硬化血脂异常的心脏代谢型(高密度脂蛋白胆固醇:比值比=10.9;<0.05)和自身免疫性甲状腺疾病(抗甲状腺过氧化物酶:比值比=5.5;<0.05);在男性中区分出两种表型:具有肝损伤酶升高的肝代谢型(胰岛素抵抗稳态模型评估:比值比=6.1;<0.05)和免疫2型反应(免疫球蛋白E:比值比=6.4;<0.05)。夫妇亚生育力的几率随着夫妇中代谢综合征实验室指标的数量增加而上升(比值比=1.7;<0.05),并且如果至少一方的总免疫球蛋白E水平升高(>100 kU/L)(比值比=6.5;<0.05)。这项研究发现,不明原因的亚生育力可能在个体和夫妇中伴随着相互重叠的免疫和代谢失调。我们建议对不明原因亚生育力的男性和女性进行一次性实验室诊断,同时考虑血脂谱、胰岛素抵抗、抗甲状腺过氧化物酶和总免疫球蛋白E。这可能允许对有针对性的医学和营养干预进行一次性评估,并有助于优化患者的健康状况。结合所得结果讨论了与亚生育力相关的肠道-器官轴。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c0fa/10531916/067279b5a4f6/jcm-12-06094-g001.jpg

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