Diagnostic Value of Stimulated Urine Luteinizing Hormone After Triptorelin Stimulation Test in Girls with Central Precocious Puberty.
Jia. Ruofan R; Xu. Zhuangjian Z; Zhou. Yuan Y; Zeng. Beilei B; Chen. Chunmei C; Huang. Panwang P; Ren. Feng F; Kong. Fan-Sheng FS; Ma. Yaping Y
Key Findings
- First 12‑hour urine LH/creatinine ≥287 IU/mol predicts CPP with 87% sensitivity and 91% specificity
- Second 12‑hour urine LH/creatinine ≥153 IU/mol predicts CPP with 92% sensitivity and 91% specificity
- Urine test AUCs (0.933 and 0.954) show strong diagnostic power
Practical Outcomes
- If blood draws are hard, a urine sample collected 12‑24 hours after a triptorelin injection can serve as a reliable marker for early puberty in girls. This method isn’t directly useful for performance or longevity hacks, but it shows how hormone tests can sometimes be done via urine instead of blood.
Summary
Researchers found that measuring luteinizing hormone in urine after a triptorelin test can accurately tell if a young girl has central precocious puberty, offering a non‑blood alternative for diagnosis.
Abstract
To investigate the diagnostic value of urine luteinizing hormone (ULH) after the triptorelin stimulation test detected by immunochemiluminometric assay (ICMA) in girls with central precocious puberty (CPP). The girls with precocious puberty were included. The triptorelin stimulation test at 8:30 a.m. was performed. Two consecutive 12-hour urine samples were collected after the test, defined as the first 12-hour and second 12-hour urine, respectively. ICMA measured ULH. Urine creatinine (Cr) concentration was measured. CPP and peripheral precocious puberty (PPP) were diagnosed by the same pediatric endocrinologist based on clinical symptoms, signs, and progression of clinical development. A total of 97 cases (CPP n=69; PPP n=28) were included, with 12 cases not meeting the receiver operating characteristic analysis criteria. The first and second 12-hour ULH/Cr in the CPP group were higher than those in the PPP group. When the first 12-hour ULH/Cr was≥287.252 IU/mol, the sensitivity and specificity for diagnosing CPP were 87.3% and 90.9%, respectively. When the second 12-hour ULH/Cr was≥152.769 IU/mol, the sensitivity and specificity for diagnosing CPP were 92.1% and 90.9%, respectively. The area under the curve of the first and second 12-hour ULH/Cr were 0.933 and 0.954, respectively. The ULH detection method after the triptorelin stimulation test has clinical significance for diagnosing CPP in girls. When blood sampling compliance in girls with precocious puberty is poor, the first 12-hour ULH/Cr≥288 IU/mol (or second 12-hour≥153 IU/mol) after the triptorelin stimulation test can serve as a laboratory indicator for diagnosis of CPP.
Study Information
pubmed
2024
2024-04-29T00:00:00.000Z
10.1055/a-2316-4772
28