Department of Neurology, First Hospital, Shanxi Medical University, No.85, Jiefang South Street, Taiyuan, China.
First Clinical Medical College, Shanxi Medical University, Taiyuan, China.
Orphanet J Rare Dis. 2024 Feb 16;19(1):72. doi: 10.1186/s13023-024-03072-6.
Late-onset multiple acyl-CoA dehydrogenase deficiency (MADD) is the most common lipid storage myopathy. There are sex differences in fat metabolism and it is not known whether late-onset MADD affects men and women equally.
In this systematic review and meta-analysis, the PubMed, Embase, Web of Science, CNKI, CBM, and Wanfang databases were searched until 01/08/2023. Studies reporting sex distribution in patients with late-onset MADD were included. Two authors independently screened studies for eligibility, extracted data, and assessed risk of bias. Pre-specified outcomes of interest were the male-to-female ratio (MFR) of patients with late-onset MADD, the differences of clinical characteristics between the sexes, and factors influencing the MFR.
Of 3379 identified studies, 34 met inclusion criteria, yielding a total of 609 late-onset MADD patients. The overall pooled percentage of males was 58% (95% CI, 54-63%) with low heterogeneity across studies (I = 2.99%; P = 0.42). The mean onset ages, diagnostic delay, serum creatine kinase (CK), and allelic frequencies of 3 hotspot variants in ETFDH gene were similar between male and female patients (P > 0.05). Meta-regressions revealed that ethnic group was associated with the MFR in late-onset MADD, and subgroup meta-analyses demonstrated that East-Asian patients had a higher percentage of male, lower CK, and higher proportion of hotspot variants in ETFDH gene than non-East-Asian patients (P < 0.05).
Male patients with late-onset MADD were more common than female patients. Ethnicity was proved to be a factor influencing the MFR in late-onset MADD. These findings suggest that male sex may be a risk factor for the disease.
迟发性多种酰基辅酶 A 脱氢酶缺乏症(MADD)是最常见的脂肪贮积性肌病。脂肪代谢存在性别差异,目前尚不清楚迟发性 MADD 是否同样影响男性和女性。
本系统评价和荟萃分析检索了 PubMed、Embase、Web of Science、CNKI、CBM 和万方数据库,检索时间截至 2023 年 1 月 8 日。纳入报道迟发性 MADD 患者性别分布的研究。两位作者独立筛选研究的纳入和排除标准,提取数据,并评估偏倚风险。预先指定的感兴趣结局是迟发性 MADD 患者的男女比例(MFR)、两性之间临床特征的差异以及影响 MFR 的因素。
在 3379 项确定的研究中,有 34 项符合纳入标准,共纳入 609 例迟发性 MADD 患者。总体上,男性的百分比为 58%(95%CI,54-63%),研究之间异质性较低(I = 2.99%;P = 0.42)。男女患者的平均发病年龄、诊断延迟、血清肌酸激酶(CK)和 ETFDH 基因 3 个热点变异的等位基因频率相似(P > 0.05)。元回归分析显示,种族与迟发性 MADD 的 MFR 相关,亚组荟萃分析表明,东亚患者的男性比例较高、CK 较低、ETFDH 基因热点变异比例较高,而非东亚患者则相反(P < 0.05)。
迟发性 MADD 男性患者比女性患者更为常见。种族被证明是影响迟发性 MADD 中 MFR 的一个因素。这些发现提示男性性别可能是该疾病的一个危险因素。