De Silva Neomal, Quinton Richard, De Silva Nipun Lakshitha, Jayasena Channa N, Barbar Bruna, Boot Chris, Wright Rohana J, Shipley Timothy W, Kanagasundaram N Suren
Department of Endocrinology & Metabolism, Newcastle-upon-Tyne Hospitals NHS Foundation Trust, Royal Victoria Infirmary, Newcastle upon Tyne, UK.
Translational & Clinical Research Institute, University of Newcastle, Newcastle upon Tyne, UK.
Clin Endocrinol (Oxf). 2025 Feb;102(2):190-195. doi: 10.1111/cen.15146. Epub 2024 Oct 6.
Anaemia is a key cause of morbidity in chronic kidney disease (CKD). Androgen deficiency (AD) in males can contribute to anaemia of all causes, including in CKD. We sought to examine the prevalence of AD in men with CKD, the extent to which it contributed to anaemia and whether it was independently associated with long-term survival.
This cross-sectional observational study was conducted among males aged 18 years and over with CKD stages 4 and 5. The study analysed morning blood samples with regard to their full blood count, urea and electrolytes, albumin, lipids, testosterone (T) and sex hormone binding globulin, with calculation of free testosterone by mass action equation. Mortality data were obtained 15 years later for survival analysis.
Among 322 patients with a mean age of 63 years, the overall prevalence of AD was 68.9%. There was a statistically significant negative correlation between erythropoiesis stimulating agent (ESA) dose and testosterone concentrations (Pearson correlation -0.193, p = 0.05). There was a positive correlation between haemoglobin (Hb) and free testosterone level among patients not on ESA therapy (Pearson correlation 0.331, p < 0.001). Kaplan-Meier plots showed p < 0.001 on log-rank analysis, indicating that AD was significantly associated with worse survival. However, in Cox regression analysis, free testosterone was not associated with survival (95% CI for free testosterone 0.997-1.000).
AD is highly prevalent among this population, and increases further with older age and more severe CKD warranting haemodialysis. Association of lower Hb and higher ESA dose with lower T concentration might be causative, which has important pharmaco-economic as well as clinical implications. Lower survival in men with low T, more likely reflects overall poor health rather than causation. A properly constituted randomised controlled study evaluating the effect of native T replacement is warranted in men with CKD and AD.
贫血是慢性肾脏病(CKD)发病的关键原因。男性雄激素缺乏(AD)可导致各种原因引起的贫血,包括CKD患者。我们旨在研究CKD男性患者中AD的患病率、其导致贫血的程度以及是否与长期生存独立相关。
这项横断面观察性研究在年龄≥18岁的CKD 4期和5期男性中进行。研究分析了早晨血样的全血细胞计数、尿素和电解质、白蛋白、血脂、睾酮(T)和性激素结合球蛋白,并通过质量作用方程计算游离睾酮。15年后获取死亡率数据进行生存分析。
在322例平均年龄63岁的患者中,AD的总体患病率为68.9%。促红细胞生成素(ESA)剂量与睾酮浓度之间存在统计学显著的负相关(Pearson相关系数为 -0.193,p = 0.05)。在未接受ESA治疗的患者中,血红蛋白(Hb)与游离睾酮水平呈正相关(Pearson相关系数为0.331,p < 0.001)。Kaplan-Meier曲线在对数秩分析中显示p < 0.001,表明AD与较差的生存率显著相关。然而,在Cox回归分析中,游离睾酮与生存无关(游离睾酮的95%置信区间为0.997 - 1.000)。
AD在该人群中高度流行,且随着年龄增长和更严重的CKD(需要血液透析)而进一步增加。较低的Hb和较高的ESA剂量与较低的T浓度之间的关联可能具有因果关系,这具有重要的药物经济学和临床意义。睾酮水平低的男性生存率较低,更可能反映整体健康状况不佳而非因果关系。有必要对CKD和AD男性进行一项设计合理的随机对照研究,以评估天然睾酮替代的效果。