Key Laboratory of Public Health Safety of Ministry of Education/School of Public Health, Fudan University, Shanghai 200032, China.
Department of Population Health Sciences, Bristol Medical School, University of Bristol, Bristol BS8 2PS, UK.
Ecotoxicol Environ Saf. 2024 Jul 1;279:116451. doi: 10.1016/j.ecoenv.2024.116451. Epub 2024 May 17.
Bile acid homeostasis is critical to human health. Low-level exposure to antibiotics has been suggested to potentially disrupt bile acid homeostasis by affecting gut microbiota, but relevant data are still lacking in humans, especially for the level below human safety threshold. We conducted a cross-sectional study in 4247 Chinese adults by measuring 34 parent antibiotics and their metabolites from six common categories (i.e., tetracyclines, qinolones, macrolides, sulfonamides, phenicols, and lincosamides) and ten representative bile acids in fasting morning urine using liquid chromatography coupled to mass spectrometry. Daily exposure dose of antibiotics was estimated from urinary concentrations of parent antibiotics and their metabolites. Urinary bile acids and their ratios were used to reflect bile acid homeostasis. The estimated daily exposure doses (EDED) of five antibiotic categories with a high detection frequency (i.e., tetracyclines, qinolones, macrolides, sulfonamides, and phenicols) were significantly associated with urinary concentrations of bile acids and decreased bile acid ratios in all adults and the subset of 3898 adults with a cumulative ratio of antibiotic EDED to human safety threshold of less than one. Compared to a negative detection of antibiotics, the lowest EDED quartiles of five antibiotic categories and four individual antibiotics with a high detection frequency (i.e., ciprofloxacin, ofloxacin, trimethoprim, and florfenicol) in the adults with a positive detection of antibiotics had a decrease of bile acid ratio between 6.6% and 76.6%. Except for macrolides (1.2×10 ng/kg/day), the medians of the lowest EDED quartile of antibiotic categories and individual antibiotics ranged from 0.32 ng/kg/day to 10 ng/kg/day, which were well below human safety thresholds. These results suggested that low-level antibiotic exposure could disrupt bile acid homeostasis in adults and existing human safety thresholds may be inadequate in safeguarding against the potential adverse health effects of low-level exposure to antibiotics.
胆汁酸稳态对人类健康至关重要。低水平接触抗生素被认为可能通过影响肠道微生物群来破坏胆汁酸稳态,但人类相关数据仍然缺乏,特别是在低于人类安全阈值的水平下。我们通过测量 4247 名中国成年人空腹晨尿中的 34 种母体抗生素及其六种常见类别(即四环素类、喹诺酮类、大环内酯类、磺胺类、苯氧羧酸类和林可酰胺类)和十种代表性胆汁酸,使用液相色谱-质谱联用技术进行了一项横断面研究。抗生素的日暴露剂量是根据母体抗生素及其代谢物的尿浓度来估计的。尿胆汁酸及其比值用于反映胆汁酸稳态。在所有成年人和抗生素日暴露剂量与人类安全阈值累积比小于 1 的 3898 名成年人亚组中,五种高检出频率的抗生素类别(即四环素类、喹诺酮类、大环内酯类、磺胺类和苯氧羧酸类)的估计日暴露剂量(EDED)与尿胆汁酸浓度显著相关,并降低了所有成年人和抗生素亚组的胆汁酸比值。与抗生素阴性检测相比,在抗生素阳性检测的成年人中,五种抗生素类别和四种高检出频率的个体抗生素(即环丙沙星、氧氟沙星、甲氧苄啶和氟苯尼考)的最低 EDED 四分位数的胆汁酸比值降低了 6.6%至 76.6%。除了大环内酯类(1.2×10ng/kg/天),抗生素类别和个体抗生素最低 EDED 四分位数的中位数范围从 0.32ng/kg/天至 10ng/kg/天,远低于人类安全阈值。这些结果表明,低水平抗生素暴露可能会破坏成年人的胆汁酸稳态,而现有的人类安全阈值可能不足以防止低水平接触抗生素的潜在不良健康影响。