Walravens Joeri, Sleumer Bas, Vos Michel J, Snaterse Gido, Narinx Nick, Antonio Leen, Reyns Tim, Fiers Tom, Kema Ido P, Kaufman Jean-Marc, van de Merbel Nico C, Lapauw Bruno
Department of Endocrinology, Ghent University Hospital, 9000 Ghent, Belgium.
ICON Bioanalytical Laboratories, 9407 TK, Assen, The Netherlands.
J Clin Endocrinol Metab. 2025 Feb 18;110(3):e641-e649. doi: 10.1210/clinem/dgae280.
Genetic variation in SHBG structure may affect estimates of sex steroid exposure by altering the affinity of the protein for its ligand. Consequently, free hormone calculations assuming constant binding affinity may, for certain genetic variations, lead to incorrect diagnoses if genetic variation is not taken into consideration.
To investigate the effects of genetic variation in SHBG on calculated and measured serum free testosterone (T) in men.
DESIGN, SETTING AND PARTICIPANTS: Population-based sibling-pair study in 999 healthy men aged 25 to 45 (mean, 34.5) years.
Genotyping using microarray (Illumina) for single-nucleotide polymorphism (SNPs) suggested to affect binding affinity and/or concentration of SHBG or T. SHBG concentrations were measured using immunoassay and in a subset (n = 32) by liquid chromatography-tandem mass spectrometry (LC-MS/MS). Total T was measured using LC-MS/MS. Free T was calculated and in a subset (n = 314) measured directly using LC-MS/MS after equilibrium dialysis.
Allelic frequencies of analyzed SNPs ranged from 0.5% to 58.2%. Compared to wild-type, SHBG concentrations were lower in rs6258 heterozygotes (-24.7%; P < .05) and higher in rs6259 heterozygotes, rs727428 homozygotes, and carriers of rs1799941 (+10.8 to 23.1%; all P < .05). Total T was higher in rs727428 homozygotes and carriers of rs5934505, rs1799941and rs6259 (+3.9 to 21.4%; all P < .05). No clear effects on measured free T were found, except for a trend toward higher values in rs6259 homozygotes, significant for calculated free T (+18.7%; P < .05) in the larger global study population.
In these men, analyzed SNPs were relatively prevalent and affected serum concentrations of total T and SHBG but not calculated or measured free T except for a higher trend in rs6259 homozygotes.
性激素结合球蛋白(SHBG)结构的基因变异可能通过改变该蛋白对其配体的亲和力来影响性类固醇暴露的评估。因此,如果不考虑基因变异,对于某些基因变异而言,假设结合亲和力恒定的游离激素计算可能会导致错误诊断。
研究SHBG基因变异对男性血清游离睾酮(T)计算值和测量值的影响。
设计、地点和参与者:对999名年龄在25至45岁(平均34.5岁)的健康男性进行基于人群的同胞对研究。
使用微阵列(Illumina)对单核苷酸多态性(SNP)进行基因分型,这些SNP被认为会影响SHBG或T的结合亲和力和/或浓度。使用免疫测定法测量SHBG浓度,并在一个亚组(n = 32)中通过液相色谱-串联质谱法(LC-MS/MS)进行测量。使用LC-MS/MS测量总T。计算游离T,并在一个亚组(n = 314)中在平衡透析后使用LC-MS/MS直接测量。
分析的SNP的等位基因频率范围为0.5%至58.2%。与野生型相比,rs6258杂合子的SHBG浓度较低(-24.7%;P < 0.05),而rs6259杂合子、rs727428纯合子和rs1799941携带者的SHBG浓度较高(+10.8%至23.1%;所有P < 0.05)。rs727428纯合子以及rs5934505、rs1799941和rs6259携带者的总T较高(+3.9%至21.4%;所有P < 0.05)。未发现对测量的游离T有明显影响,除了在rs6259纯合子中有升高趋势,在更大的全球研究人群中,计算的游离T显著升高(+18.7%;P < 0.05)。
在这些男性中,分析的SNP相对普遍,影响总T和SHBG的血清浓度,但除了rs6259纯合子有升高趋势外,不影响计算的或测量的游离T。