Key result
Comorbid T2D and HTN linked to greater brain structural disruptions and aging deviations than neither condition.
Why the study?
Higher prevalence of hypertension and type 2 diabetes in Puerto Rican older adults compared to non-Hispanic White adults may contribute to disparities in brain structural integrity and cognition.
Does the comorbidity of hypertension and type 2 diabetes worsen brain structural integrity and cognitive capacity in Puerto Rican older adults compared to those without these conditions or non-Hispanic White adults?
Cohort
Yes
Does the comorbidity of hypertension and type 2 diabetes worsen brain structural integrity and cognitive capacity in Puerto Rican older adults compared to those without these conditions or non-Hispanic White adults?
The comorbidity of type 2 diabetes and hypertension is associated with greater brain structural disruptions and cognitive impairment than hypertension alone, potentially contributing to health disparities in the Puerto Rican population.
Answers are grounded in this paper and cite their sources.
May heighten cognitive risk in comorbid Puerto Rican adults; leaves open causal mechanisms and intervention targets.
BACKGROUND AND OBJECTIVES: The Boston Puerto Rican Health Study (BPRHS) is a longitudinal study following self-identified Puerto Rican older adults living in the Greater Boston area. Studies have shown higher prevalence of hypertension (HTN) and type 2 diabetes (T2D) within this ethnic group compared to age-matched non-Hispanic White adults. In this study, we investigated the associations of HTN and T2D comorbidity on brain structural integrity and cognitive capacity in community-dwelling Puerto Rican adults and compared these measures with older adult participants (non-Hispanic White and Hispanic) from the Alzheimer's Disease Neuroimaging Initiative (ADNI) and National Alzheimer's Coordinating Center (NACC) databases. METHODS: BPRHS participants who underwent brain MRI and cognitive testing were divided into 4 groups based on their HTN and T2D status: HTN-/T2D-, HTN+/T2D-, HTN-/T2D+, and HTN+/T2D+. We assessed microstructural integrity of white matter (WM) pathways using diffusion MRI, brain macrostructural integrity using hippocampal volumes, and brain age using T1-weighted MRI and cognitive test scores. BPRHS results were then compared with results from non-Hispanic White and Hispanic participants from the ADNI and NACC databases. RESULTS: The prevalence of HTN was almost 2 times (66.7% vs 38.7%) and of T2D was 5 times (31.8% vs 6.6.%) higher in BPRHS than in ADNI non-Hispanic White participants. Diffusion MRI showed clear deterioration patterns in major WM tracts in the HTN+/T2D+ group and, to a lesser extent, in the HTN+/T2D- group compared to the HTN-/T2D- group. HTN+/T2D+ participants also had the smallest hippocampal volume and larger brain aging deviations. Trends toward lower executive function and global cognitive scores were observed in HTN+/T2D+ relative to HTN-/T2D- individuals. MRI measures and the Mini-Mental State Examination (MMSE) scores from the HTN+/T2D+ BPRHS group resembled those of ADNI White participants with progressive mild cognitive impairment (MCI), while the BPRHS HTN-/T2D- participants resembled participants with stable MCI. The BPRHS was not significantly different from the ADNI + NACC Hispanic cohort on imaging or MMSE measures. DISCUSSION: The effects of T2D and HTN comorbidity led to greater brain structural disruptions than HTN alone. The high prevalence of HTN and T2D in the Puerto Rican population may be a key factor contributing to health disparities in cognitive impairment in this group compared to non-Hispanic White adults in the same age range. TRIAL REGISTRATION INFORMATION: ClinicalTrials.gov identifier: NCT01231958.
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A 2022 study conducted a cohort in Hypertension and Type 2 Diabetes. Hypertension and Type 2 Diabetes vs. No hypertension and no type 2 diabetes was evaluated on Brain structural integrity and cognitive capacity. Comorbid diabetes and hypertension, highly prevalent in Puerto Rican adults (HTN 66.7%, T2D 31.8%), was associated with greater brain structural disruptions and aging deviations than neither condition.
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