Assessing Iodine Deficiency and Halide Levels in Brevard County, Florida: A Retrospective Practice Audit

Stefan Hartmann *
Stefan Hartmann
Corresponding Author

Affiliation: Iron Direct Primary Care

Email: ironmedicinepa@gmail.com

Isabella Hartmann
Isabella Hartmann

Affiliation: Iron Direct Primary Care

Pierre Cloutier
Pierre Cloutier

Affiliation: Iron Direct Primary Care

Abstract


This retrospective practice audit explored iodine deficiency and halide levels in Brevard County, Florida, using patient data from Iron Direct Primary Care. The study analyzed random urine iodine concentrations from a combined cohort (N=116, excluding known high exogenous intake), serum iodine levels (N=49), and iodine challenge tests (N=36). The median urinary iodine concentration (UIC) for the non-exogenous cohort was 88.8 µg/L, indicating mild iodine deficiency by WHO standards. Overall, 57.8% of this cohort exhibited UIC below the WHO’s adequate threshold of 100 µg/L, with varying degrees of deficiency. Serum iodine analysis (N=49) revealed a median value of 46.6 µg/L, suggesting low iodine status. All 36 participants in the iodine challenge test excreted less than 90% of a 50mg iodine dose (mean excretion 63.0%), suggesting widespread iodine insufficiency and showing evidence of fluoride and bromide displacement. Gender-specific analysis of non-exogenous random urine iodine levels showed no statistically significant difference in mean concentrations between males and females (p=0.341). The study underscores the need for public health interventions, including consideration of iodine supplementation strategies and halide competition in assessing iodine status. The findings advocate for increased awareness to combat health risks associated with iodine deficiency and support public health policy interventions to limit exposure to iodine receptor competitors fluoride and bromide that the WHO standards for iodine sufficiency are too low.

Introduction


 Iodine, indispensable for thyroid hormone production, influences metabolism, growth, and neurodevelopment (Bonofiglio & Catalano, 2020). Despite the importance of maintaining optimal levels of iodine, iodine deficiency remains prevalent, potentially causing health issues such as goiter, hypothyroidism, developmental delays, fibrocystic breast diseases, and an increased risk of cancerous growths of the breast, thyroid, uterus, and prostate (Zimmerman et al., 2009). Moreover, comprehensive epidemiological data on iodine status within regions of the U.S. population have been relatively scarce since foundational national surveys such as those reported by Hollowell et al. (1998), highlighting the ongoing need for contemporary regional assessments. This study evaluated iodine status by analyzing results from random urine iodine tests, serum iodine tests, and iodine challenge tests from patients at a primary care practice in Brevard County, Florida, to determine the prevalence of iodine deficiency and explore halide interactions, discussing the implications for public health.

Methods


This study was conducted as a retrospective practice audit at Iron Direct Primary Care in Brevard County, Florida. Data were analyzed from patients who had undergone random urine iodine testing (LabCorp), serum iodine testing (LabCorp), and/or urine halide challenge testing (Doctors Data) between May 2021 and December 2024.

Participants and Data Sources

Participants were patients of Iron Direct Primary Care, a primary care practice that utilizes iodine assessment as part of routine screening. All patients whose lab records were included in this study had reportedly consumed iodine at Recommended Dietary Allowance (RDA) levels through dietary sources such as iodized salt, multivitamins, or seafood (based on patient self-report). All participants lived within a few miles of the Atlantic Ocean. No external funding was received, and no conflicts of interest were involved; patients independently paid for all lab tests.

The datasets analyzed were as follows:

Random Urine Iodine (LabCorp): Data from 83 random urine iodine tests were included.

Serum Iodine (LabCorp): Data from 49 serum iodine tests were included.

Iodine Challenge Test (Doctors Data): Data from 36 patients who completed the iodine challenge test were analyzed. This test includes a pre-challenge spot urine sample and a 24-hour post-load urine collection.

Combined Random/Spot Urine Iodine Analysis Cohort: For assessing the overall prevalence of iodine deficiency using spot urine concentrations, data from the LabCorp random urine tests (N=83) and the pre-challenge urine samples from the Doctors Data halide test (N=35 valid pre-test values from 36 participants) were combined. From this total of 118 samples, 2 samples with exceptionally high iodine levels (>600 µg/L, indicative of recent high exogenous intake) were excluded, resulting in a cohort of N=116 for this specific analysis.

Data Collection: Random urine iodine concentrations (UIC), serum iodine concentrations, and iodine challenge test results (including pre- and post-load urinary iodine, bromide, and fluoride, and percent iodine excretion) were measured.

Ethical Considerations: In accord with 45 CFR 46 and the 22 July 2025 OHRP correspondence, the IPAK Institutional Review Board confirmed and awarded “Exempt” status to protocol 2025-0723-HARTMANN-IODINE, IRB00014237, effective 24 July 2025. This study was a retrospective audit of existing patient records from routine clinical care and involved no new interventions. Patient data were de-identified prior to analysis to ensure confidentiality, and the research did not alter patient care or pose additional risks.

Statistical Analysis: Data were analyzed for mean, median, standard deviation (SD), minimum, maximum, and interquartile range (IQR). Prevalence of iodine deficiency was categorized using WHO criteria (UIC: Severe <20 µg/L, Moderate 20-49 µg/L, Mild 50-99 µg/L, Adequate 100-199 µg/L). A two-sample t-test, preceded by Levene’s test for equality of variances, was used to compare mean urine iodine concentrations between genders. Statistical significance was set at p 0.05.

Results


Urinary Iodine Concentrations (Non-Exogenous Combined Cohort, N=116):
Analysis of the combined random and pre-challenge spot urine iodine samples (N=116), after excluding two presumed exogenous users (UIC > 600 µg/L), yielded the following:
Mean UIC: 121.91 µg/L
Median UIC: 88.8 µg/L
Standard Deviation: 98.23 µg/L
Range: 0.0 µg/L to 446.5 µg/L
IQR: 62.45 µg/L (25th percentile) to 150.95 µg/L (75th percentile). The median UIC of 88.8 µg/L indicates mild iodine deficiency in this cohort according to WHO standards.

Distribution of Iodine Levels (Non-Exogenous Combined Cohort, N=116) per WHO standards:
Severe Deficiency (<20 µg/L): 4 samples (3.4%)
Moderate Deficiency (20-49 µg/L): 21 samples (18.1%)
Mild Deficiency (50-99 µg/L): 42 samples (36.2%)
Total with Deficiency (100 µg/L): 67 samples (57.8%)
Adequate (100-199 µg/L): 24 samples (20.7%)
More than Adequate (200-600 µg/L): 25 samples (21.6%)

Gender Analysis (Non-Exogenous Combined Cohort Urine Iodine):
This dataset included 42 males and 41 females with available gender information.
Mean Iodine Males (N=42): 95.79 µg/L
Mean Iodine Females (N=41): 115.44 µg/L A two-sample t-test found no statistically significant difference in mean urine iodine concentrations between males and females (t = -0.958, p = 0.341; Levene test p=0.515).

Serum Iodine (N=49):
Mean Serum Iodine: 48.64 µg/L
Median Serum Iodine: 46.6 µg/L
Standard Deviation: 14.52 µg/L
Range: 27.5 µg/L to 107.0 µg/L
IQR: 40.8 µg/L to 52.9 µg/L

Iodine Challenge Test (N=36):
All 36 participants excreted less than 90% of the 50mg iodine/iodide load over 24 hours, indicating iodine insufficiency.
Mean Iodine Excretion: 63.0%
Median Iodine Excretion: 65.0%
Standard Deviation: 10.27%
Range: 44.0% to 80.0%

Pre-Challenge Urine Halides (N=36 cohort):
Iodine (N=35 valid pre-test samples):
Mean UIC: 182.7 µg/L (after conversion from µg/mL)
Median UIC: 140.0 µg/L (Note: This specific subgroup analysis for pre-challenge iodine includes individuals who might be on exogenous iodine; one patient had a pre-challenge value of 1800 µg/L).

Bromine (µg/mL, N=34 valid data):
Mean: 2.50; Median: 1.85; SD: 1.88; Range: 0.28 – 7.4

Fluoride (µg/mL, N=34 valid data):
Mean: 0.57; Median: 0.52; SD: 0.29; Range: 0.2 – 1.2

Post-Challenge Urine Halides (N=36 cohort):
Bromine (mg/24 hr, N=34 valid data):
Mean: 3.57; Median: 2.75; SD: 2.29; Range: 1.1 – 11.0

Fluoride (mg/24 hr, N=33 valid data):
Mean: 0.90; Median: 0.7; SD: 0.61; Range: 0.28 – 3.5. Observation of pre- and post-challenge halide levels suggests displacement occurred

Discussion


 This retrospective practice audit conducted in Brevard County, Florida, provides significant insights into local iodine nutritional status and the potential impact of competing halides. The analysis of 116 spot/random urine samples (excluding individuals with high exogenous iodine intake) revealed a median urinary iodine concentration (UIC) of 88.8 µg/L. This central tendency positions the studied cohort within the mild iodine deficiency range according to World Health Organization (WHO) criteria (WHO, 2024). Critically, 57.8% of these individuals exhibited UIC levels below the 100 µg/L threshold, indicating that a majority may not be achieving iodine adequacy. These findings are noteworthy and align with broader concerns about iodine status, as highlighted by research from Zimmerman et al. (2009) and Caldwell et al. (2011), which documented trends of suboptimal iodine levels even within developed nations.

Further supporting these observations, serum iodine data from 49 participants showed a median of 46.6 µg/L, indicative of low iodine status in this group, although serum iodine is recognized as a less sensitive measure for population assessment compared to UIC. The investigation into gender-based differences in non-exogenous urine iodine revealed no statistically significant disparity in mean UIC between males and females (p=0.341), suggesting that the observed patterns of iodine insufficiency are prevalent across genders within this patient sample.

The Iodine Challenge Test, performed on 36 participants, offered compelling evidence of iodine insufficiency. This test evaluates iodine status by quantifying the 24-hour urinary excretion of a 50mg oral iodine/iodide load; lower excretion (typically <90%) signifies bodily retention due to need. Strikingly, all 36 participants in this study excreted less than 90% of the administered dose, with a mean excretion of only 63.0%. Such universal retention underscores a widespread physiological demand for iodine among these individuals.

A key aspect of the Iodine Challenge Test is its utility in elucidating competitive halide dynamics. Following iodine loading, an increased urinary output of both bromide (mean pre-challenge 2.50 µg/mL vs. mean post-challenge 3.57 mg/24 hr) and fluoride (mean pre-challenge 0.57 µg/mL vs. mean post-challenge 0.90 mg/24 hr) was observed. While differences in pre- and post-challenge units make direct quantitative comparison of excretion rates challenging without pre-challenge 24-hour urine volumes, the pattern of increased halide detection in 24-hour post-load urine is suggestive of displacement by iodine. This finding is consistent with established mechanisms whereby halogens like fluoride and bromide competitively inhibit iodine uptake, particularly at the sodium-iodide symporter (NIS) in the thyroid gland, potentially impairing thyroid function (Waugh, 2019). The presence of these halides could therefore exacerbate existing iodine deficiencies or functionally increase an individual’s iodine requirement. This is particularly relevant given contemporary environmental exposures and local public health discussions, such as those concerning water fluoridation policies in Florida. Literature, such as the study by Kheradpisheh et al. (2018), has also indicated a negative impact of fluoride on thyroid hormone parameters even at standard concentrations.

Clinical observations from this primary care setting suggest that iodine supplementation, often at doses exceeding the standard RDA (e.g., 6-12mg daily or higher), is frequently well-tolerated and associated with patient-reported improvements in conditions sometimes linked to iodine deficiency, such as fibrocystic breast symptoms (Ghent et al., 1993), fatigue, and cognitive difficulties. These clinical experiences, while anecdotal to this audit, underscore the perceived importance of addressing iodine insufficiency. The occasional report of transient symptoms during initial iodine supplementation, possibly related to halide mobilization, is an area that merits further systematic investigation. The adjunctive use of selenium is often considered in iodine repletion protocols, reflecting its crucial roles in thyroid hormone conversion and antioxidant protection within the thyroid gland (Negro et al., 2007; Wichman et al., 2016).

The findings of widespread deficiency and insufficiency in a patient population reportedly consuming RDA levels of iodine lend credence to the hypothesis that current RDAs (e.g., 150 µg/day for most adults) may not be adequate for all individuals, particularly in environments with notable exposure to competing halides that can impair iodine absorption or utilization, as theorized by Waugh (2019).

The prevalence of iodine deficiency and insufficiency identified in this Brevard County cohort has notable public health implications. Iodine’s essentiality extends beyond thyroid hormone synthesis to encompass broad roles in metabolic regulation, neurodevelopment (critically for fetal and early childhood stages), and potentially in mitigating risks for certain hormone-sensitive cancers (Zimmerman et al., 2009; Bonofiglio & Catalano, 2020). These results highlight a need for enhanced awareness among healthcare providers and the public regarding optimal iodine nutrition. Potential strategies could involve dietary counseling, more targeted approaches to iodine supplementation (especially where halide exposure is a factor), and ongoing surveillance of iodine status within the community. The data also support broader public health considerations aimed at minimizing exposure to unnecessary environmental halides.

Limitations

This study, being a retrospective practice audit, has inherent limitations. The patient sample was derived from a single primary care practice, potentially limiting generalizability to the wider Brevard County population. Self-reported dietary iodine intake at RDA levels could not be independently verified. While multiple iodine assessment metrics were employed, comprehensive thyroid function panels (TSH, free T3, free T4, thyroid antibodies) were not systematically available for all participants to directly correlate iodine status with thyroid function parameters within the scope of this audit. The evidence for halide displacement is inferred from excretion patterns and known physiological mechanisms, rather than direct measures of tissue halide concentrations or NIS activity. Furthermore, differing units for pre-challenge (concentration) versus post-challenge (24-hour total excretion) halide measurements make direct quantitative comparisons of excretion rate changes complex without pre-challenge 24-hour urine volume data.

Future Research

To build upon these findings, prospective studies employing larger, more representative community samples are warranted to ascertain the broader prevalence of iodine deficiency and to quantify halide exposure levels. Research that incorporates comprehensive thyroid function testing alongside iodine and halide assessments would provide a more complete understanding of the physiological impacts. Intervention studies are needed to evaluate the efficacy, safety, and optimal dosing of various iodine supplementation strategies, particularly in relation to halide exposure and the potential benefits of co-factors like selenium. Further investigation into the clinical phenomena associated with halide mobilization during iodine therapy could also yield valuable clinical insights.

Acknowledgments


Stefan Hartmann extracted the lab values and was the primary author of the manuscript.
Isabella Hartmann contributed to the literature review and statistical analysis.
Pierre Cloutier offered guidance on the overall format and provided his extensive knowledge on the role of the elements and their role in human physiology.

References


Bonofiglio, D., & Catalano, S. (2020). Effects of iodine intake on human health. MDPI.

Caldwell, K. L., Makhmudov, A., Ely, E., Jones, R. L., & Wang, R. Y. (2011). Iodine status of the U.S. population, National Health and Nutrition Examination Survey, 2005–2006 and 2007–2008. Thyroid, 21(4), 419–427. https://doi.org/10.1089/thy.2010.0077

Ghent, W. R., Eskin, B. A., Low, D. A., & Hill, L. P. (1993). Iodine replacement in fibrocystic disease of the breast. Canadian Journal of Surgery, 36(5), 453–460.

Hollowell, J. G., Staehling, N. W., Hannon, W. H., Flanders, D. W., Gunter, E. W., Maberly, G. F., Braverman, L. E., & Trowbridge, F. L. (1998). Iodine nutrition in the United States. Trends and public health implications: Iodine excretion data from National Health and Nutrition Examination Surveys I and III (1971-1974 and 1988-1994). The Journal of Clinical Endocrinology & Metabolism, 83(10), 3401–3408. https://doi.org/10.1210/jcem.83.10.5169

Kheradpisheh, Z., Mirzaei, M., Mahvi, A. H., Mokhtari, M., Azizi, R., Fallahzadeh, H., & Ehrampoush, M. H. (2018). Impact of Drinking Water Fluoride on Human Thyroid Hormones: A Case-Control Study. Scientific Reports, 8(1), Article 2674. https://doi.org/10.1038/s41598-018-20696-4

Negro, R., Greco, G., Mangieri, T., Pezzarossa, A., Dazzi, D., & Hassan, H. (2007). The Influence of Selenium Supplementation on Postpartum Thyroid Status in Pregnant Women with Thyroid Peroxidase Autoantibodies. The Journal of Clinical Endocrinology & Metabolism, 92(4), 1263–1268 https://doi.org/10.1210/jc.2006-1805

Waugh, D. T. (2019). Fluoride Exposure Induces Inhibition of Sodium/Iodide Symporter (NIS) Contributing to Impaired Iodine Absorption and Iodine Deficiency: Molecular Mechanisms of Inhibition and Implications for Public Health. International Journal of Environmental Research and Public Health, 16(6), Article 1086. https://doi.org/10.3390/ijerph16061086

Wichman, J. E., Winther, K. H., Bonnema, S. J., & Hegedüs, L. (2016). Selenium Supplementation Significantly Reduces Thyroid Autoantibody Levels in Patients with Chronic Autoimmune Thyroiditis: A Systematic Review and Meta-Analysis. Thyroid, 26(12), 1681–1692 https://doi.org/10.1089/thy.2016.0256

World Health Organization. (2024). Iodine deficiency. Retrieved March 10, 2025, from https://www.who.int/data/nutrition/nlis/info/iodine-deficiency

Zimmerman, M. B., Jooste, P. L., & Pandav, C. S. (2009). Iodine deficiency. Endocrine Reviews, 30(4), 376–408. https://doi.org/10.1210/er.2009-0011

Subscribe to SciPublHealth


Science-based knowledge, not narrative-dictated knowledge, is the goal of WSES, and we will work to make sure that only objective knowledge is used in the formation of medical standards of care and public health policies.

About this paper


Cite this paper

Hartmann S, Hartmann I, Cloutier P. Assessing Iodine Deficiency and Halide Levels in Brevard County, Florida: A Retrospective Practice Audit. Science, Public Health Policy and the Law. 2025 Oct 01; v8.2019-2025

  • Feds for Freedom

Discover more from Science, Public Health Policy and the Law

Subscribe now to keep reading and get access to the full archive.

Continue reading