Bone mass, microarchitecture and turnover among young Indian women with non-alcoholic fatty liver disease.

IF 3 3区 医学 Q2 ENDOCRINOLOGY & METABOLISM
Endocrine Pub Date : 2024-11-01 Epub Date: 2024-06-24 DOI:10.1007/s12020-024-03934-w
Alpesh Goyal, Suraj Kubihal, Yashdeep Gupta, Shalimar, Devasenathipathy Kandasamy, Mani Kalaivani, Nikhil Tandon
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引用次数: 0

Abstract

Purpose: To evaluate comprehensive bone health among young Indian women, including bone mass, microarchitecture, and turnover, in relation to their non-alcoholic fatty liver disease (NAFLD) status.

Methods: This cross-sectional study (May 2018-November 2019) recruited women with a history of gestational diabetes mellitus (GDM) and normoglycemia in their index pregnancy, who were at least 6 months postpartum. All participants underwent abdominal ultrasonography for determination of NAFLD status (grades 2 and 3: severe NAFLD) and transient elastography (FibroScan) for hepatic fibrosis (LSM >6 kPa). Bone mass was assessed by DXA, bone microarchitecture with trabecular bone score {TBS} (low TBS ≤ 1.310) and bone turnover with markers of bone formation (osteocalcin and P1NP), and resorption (CTX).

Results: Bone mineral density (BMD) at femoral neck (p = 0.026) and total hip (p = 0.007) was significantly higher among women with NAFLD (n = 170) compared to those without (n = 124). There was no significant difference in bone turnover markers between the two groups. The presence of NAFLD [adjusted OR: 1.82 (1.07, 3.11)] was associated with low TBS, with a greater strength of association among women with severe NAFLD [adjusted OR: 2.97 (1.12, 7.88)]. However, these associations were attenuated and no longer significant after additionally adjusting for BMI. Women with NAFLD and hepatic fibrosis manifested significantly higher BMD at lumbar spine, femoral neck, and total hip (p < 0.001 for all) and significantly lower bone turnover markers (osteocalcin, p = 0.009 and CTX, p = 0.029), however, the association with low TBS was not observed.

Conclusion: Among young Indian women, NAFLD is associated with increased bone mass and impaired bone microarchitecture, and hepatic fibrosis with increased bone mass and reduced bone turnover.

Abstract Image

患有非酒精性脂肪肝的印度年轻女性的骨量、微结构和骨转换。
目的:评估印度年轻女性的综合骨健康状况,包括骨量、微结构和骨转换,并将其与非酒精性脂肪肝(NAFLD)状况联系起来:这项横断面研究(2018 年 5 月至 2019 年 11 月)招募了有妊娠期糖尿病(GDM)病史且指数孕期血糖正常、产后至少 6 个月的女性。所有参与者都接受了腹部超声波检查,以确定非酒精性脂肪肝状态(2 级和 3 级:严重非酒精性脂肪肝),并接受瞬态弹性成像(FibroScan)检查以确定肝纤维化(LSM >6 kPa)。通过 DXA 评估骨量,通过骨小梁评分{TBS}评估骨的微观结构(低 TBS ≤ 1.0 kPa)。(低 TBS ≤ 1.310)和骨形成标志物(骨钙素和 P1NP)及骨吸收标志物(CTX)评估骨转换:非酒精性脂肪肝妇女(170 人)股骨颈(P = 0.026)和全髋(P = 0.007)的骨矿物质密度(BMD)明显高于非酒精性脂肪肝妇女(124 人)。两组之间的骨转换指标没有明显差异。存在非酒精性脂肪肝[调整后 OR:1.82 (1.07, 3.11)]与低 TBS 相关,严重非酒精性脂肪肝妇女的相关性更大[调整后 OR:2.97 (1.12, 7.88)]。然而,在对体重指数(BMI)进行额外调整后,这些相关性减弱且不再显著。患有非酒精性脂肪肝和肝纤维化的女性在腰椎、股骨颈和全髋部的 BMD 明显更高(p 结论:非酒精性脂肪肝和肝纤维化的女性在腰椎、股骨颈和全髋部的 BMD 明显更高:在印度年轻女性中,非酒精性脂肪肝与骨量增加和骨微结构受损有关,而肝纤维化与骨量增加和骨转换减少有关。
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来源期刊
Endocrine
Endocrine ENDOCRINOLOGY & METABOLISM-
CiteScore
6.50
自引率
5.40%
发文量
295
审稿时长
1.5 months
期刊介绍: Well-established as a major journal in today’s rapidly advancing experimental and clinical research areas, Endocrine publishes original articles devoted to basic (including molecular, cellular and physiological studies), translational and clinical research in all the different fields of endocrinology and metabolism. Articles will be accepted based on peer-reviews, priority, and editorial decision. Invited reviews, mini-reviews and viewpoints on relevant pathophysiological and clinical topics, as well as Editorials on articles appearing in the Journal, are published. Unsolicited Editorials will be evaluated by the editorial team. Outcomes of scientific meetings, as well as guidelines and position statements, may be submitted. The Journal also considers special feature articles in the field of endocrine genetics and epigenetics, as well as articles devoted to novel methods and techniques in endocrinology. Endocrine covers controversial, clinical endocrine issues. Meta-analyses on endocrine and metabolic topics are also accepted. Descriptions of single clinical cases and/or small patients studies are not published unless of exceptional interest. However, reports of novel imaging studies and endocrine side effects in single patients may be considered. Research letters and letters to the editor related or unrelated to recently published articles can be submitted. Endocrine covers leading topics in endocrinology such as neuroendocrinology, pituitary and hypothalamic peptides, thyroid physiological and clinical aspects, bone and mineral metabolism and osteoporosis, obesity, lipid and energy metabolism and food intake control, insulin, Type 1 and Type 2 diabetes, hormones of male and female reproduction, adrenal diseases pediatric and geriatric endocrinology, endocrine hypertension and endocrine oncology.
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