Urine dicarboxylic acid as a potential AD biomarker associated with fusiform gyrus volume in older cognitively healthy adults

Abstract Background Our study aims to determine if urine dicarboxylic acids (DCA) concentrations might be associated with specific brain region volumes in older cognitively healthy (CH) adults. Method We recruited CH study participants (> 65 years) and acquired MRI data analyzed using NeuroQuant. Urine DCAs were quantified using GC‐MS. For n=62 participants, DCA variables of interest—C4+C5 and C7+C8+C9 (% of the sum of C4 to C10), and their ratio—were assessed for association with each of six intracranial volume (icv)‐normalized brain region volumes; C4+C5 with 61 additional regions. We modeled volume as a function of a discretized DCA variable (sample tertiles), age, and sex, for each pair. Pairs with a statistically significant estimated association were assessed by fitting natural cubic spline models with a range of spline degrees of freedom in a second stage of analysis. The Benjamini–Hochberg procedure was used to control the false discovery rate below q 1 = 0.2 in the first stage and q 2 = 0.05 in the second stage. Result There was a significant estimated inverse association of categorical C7+C8+C9 with the fusiform gyrus (FG) volume (Table 1). Similarly, there was a significant estimated positive association between categorical (C4+C5)/(C7+C8+C9) and FG volume (Table 1). The FG was estimated to decrease by 0.004 for every one‐unit increase in C7+C8+C9, and this estimated association remained significant after adjusting P values for all tests (95% CI ‐0.007 to 0.002; adjusted P = .035, Table 2). The observed Cohen’s f2 for the DCA variable was 0.18. For the (C4+C5)/(C7+C8+C9)–FG couple, it was the 2‐df natural cubic spline model that had the lowest Bayesian information criterion values among the spline models considered, with a significant estimated association of the DCA variable with the FG (spline adjusted P = 0.035). Figure 1 depicts the estimated spline. The observed Cohen’s f2 for the spline was 0.29. Conclusion Our analysis suggests that DCA metabolism may be associated with FG volume differences between individuals. Since the FG participates in visual processing, memory, and multisensory integration, urinary DCA levels may be biomarkers to monitor AD pathophysiology associated with differences in these functions.

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Journal
Alzheimer s & Dementia
Published
2024-12-01
DOI
https://doi.org/10.1002/alz.091892
Citations
1
Primary Topic
Cerebrovascular and Carotid Artery Diseases
Type
article
Field-Weighted Citation Impact
0.42
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article

Urine dicarboxylic acid as a potential AD biomarker associated with fusiform gyrus volume in older cognitively healthy adults

Wendy Jean Mack, Jimmy J.H. Kang, Robert A. Kloner, Thomas Macias et al.
1 citations
Alzheimer s & Dementia
Cerebrovascular and Carotid Artery Diseases
0.42
article

Urine dicarboxylic acid as a potential AD biomarker associated with fusiform gyrus volume in older cognitively healthy adults

Wendy Jean Mack, Jimmy J.H. Kang, Robert A. Kloner, Thomas Macias, Yafa Minazad, Anne Nolty, Alfred N. Fonteh, Yongxin Yu, Salvador Horacio Guzmán-Maldonado, Xianghong Arakaki, Ryan K. Butler, Helena C. Chui
article en
1 citations

Abstract

Abstract Background Our study aims to determine if urine dicarboxylic acids (DCA) concentrations might be associated with specific brain region volumes in older cognitively healthy (CH) adults. Method We recruited CH study participants (> 65 years) and acquired MRI data analyzed using NeuroQuant. Urine DCAs were quantified using GC‐MS. For n=62 participants, DCA variables of interest—C4+C5 and C7+C8+C9 (% of the sum of C4 to C10), and their ratio—were assessed for association with each of six intracranial volume (icv)‐normalized brain region volumes; C4+C5 with 61 additional regions. We modeled volume as a function of a discretized DCA variable (sample tertiles), age, and sex, for each pair. Pairs with a statistically significant estimated association were assessed by fitting natural cubic spline models with a range of spline degrees of freedom in a second stage of analysis. The Benjamini–Hochberg procedure was used to control the false discovery rate below q 1 = 0.2 in the first stage and q 2 = 0.05 in the second stage. Result There was a significant estimated inverse association of categorical C7+C8+C9 with the fusiform gyrus (FG) volume (Table 1). Similarly, there was a significant estimated positive association between categorical (C4+C5)/(C7+C8+C9) and FG volume (Table 1). The FG was estimated to decrease by 0.004 for every one‐unit increase in C7+C8+C9, and this estimated association remained significant after adjusting P values for all tests (95% CI ‐0.007 to 0.002; adjusted P = .035, Table 2). The observed Cohen’s f2 for the DCA variable was 0.18. For the (C4+C5)/(C7+C8+C9)–FG couple, it was the 2‐df natural cubic spline model that had the lowest Bayesian information criterion values among the spline models considered, with a significant estimated association of the DCA variable with the FG (spline adjusted P = 0.035). Figure 1 depicts the estimated spline. The observed Cohen’s f2 for the spline was 0.29. Conclusion Our analysis suggests that DCA metabolism may be associated with FG volume differences between individuals. Since the FG participates in visual processing, memory, and multisensory integration, urinary DCA levels may be biomarkers to monitor AD pathophysiology associated with differences in these functions.

Alzheimer s & DementiaVol. 20(S2)
University of Southern California (US), Huntington Medical Research Institutes (US), Texas Neurology (US), Fuller Theological Seminary (US)
Openalex Percentile: Top 29%
Cerebrovascular and Carotid Artery Diseases
0.42
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