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Sample Size and Optimal Timing for Urine Collection Based on Diurnal Variability of Urinary Iodine/Creatinine Ratio
1Department of Nutrition and Food Hygiene, School of Public Health, Tianjin Medical University, Tianjin, 300070, China.
Urinary iodine concentration (UIC) is influenced by variable urine volume, undermining its reliability. The urinary iodine/creatinine ratio (UI/Cr) may provide a more stable measure, especially in pregnancy. This study aimed to explore the variation of UI/Cr in assessing iodine status in pregnant women, and determine the sample size and optimal sampling time for accurate assessment. Thirteen pregnant women participated in a seven-day iodine metabolism study. All urine samples from each participant were collected separately over the 7-day period, and urinary iodine and urinary creatinine were tested. Spot UIC was positively correlated with time interval (β = 12.09, P < 0.001). UI/Cr, an indicator corrected for volume effect, showed no significant effect with time interval (β = -3.00, P = 0.090). The CV of UI/Cr was lower than UIC at both individual (56.16% vs. 73.15%) and population levels (62.41% vs. 84.75%). With a 95% confidence interval and ± 20% precision, an individual needs 33 urine samples, while a population requires 39 samples. The mixed-effects model analysis revealed that spot UI/Cr during the 18:00-23:59 period exhibited the strongest correlation with 24-hour UI/Cr (β = 0.62, P < 0.001). Additionally, spot UI/Cr during the 12:00-17:59 period demonstrated the strongest correlation with 24-hour urinary iodine excretion (β = 0.61, P < 0.001). The UI/Cr provides a more reliable estimate of iodine status than UIC. To obtain a precision of ± 20%, 33 spot-urine samples are required for individual assessment and 39 for population-level evaluation. We recommend urine collection between 12:00 and 18:00 for accurate evaluation.
Urinary iodine concentration (UIC) is influenced by variable urine volume, undermining its reliability. The urinary iodine/creatinine ratio (UI/Cr) may provide a more stable measure, especially in pregnancy. This study aimed to explore the variation of UI/Cr in assessing iodine status in pregnant women, and determine the sample size and optimal sampling time for accurate assessment. Thirteen pregnant women participated in a seven-day iodine metabolism study. All urine samples from each participant were collected separately over the 7-day period, and urinary iodine and urinary creatinine were tested. Spot UIC was positively correlated with time interval (β = 12.09, P < 0.001). UI/Cr, an indicator corrected for volume effect, showed no significant effect with time interval (β = -3.00, P = 0.090). The CV of UI/Cr was lower than UIC at both individual (56.16% vs. 73.15%) and population levels (62.41% vs. 84.75%). With a 95% confidence interval and ± 20% precision, an individual needs 33 urine samples, while a population requires 39 samples. The mixed-effects model analysis revealed that spot UI/Cr during the 18:00-23:59 period exhibited the strongest correlation with 24-hour UI/Cr (β = 0.62, P < 0.001). Additionally, spot UI/Cr during the 12:00-17:59 period demonstrated the strongest correlation with 24-hour urinary iodine excretion (β = 0.61, P < 0.001). The UI/Cr provides a more reliable estimate of iodine status than UIC. To obtain a precision of ± 20%, 33 spot-urine samples are required for individual assessment and 39 for population-level evaluation. We recommend urine collection between 12:00 and 18:00 for accurate evaluation.
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