# ADHD and adherence to antihypertensive medication treatment: a multinational cohort study

**Authors:** Honghui Yao, Yiling Zhou, Lin Li, Malcolm B. Gillies, Isabell Brikell, Le Gao, Theresa Wimberley, Tian Xie, Yanli Zhang-James, Aske Astrup, Søren Dalsgaard, Birgitte Dige Semark, Anders Engeland, Stephen V. Faraone, Kari Klungsøyr, Henrik Larsson, Kenneth K. C. Man, Harold Snieder, Ian C. K. Wong, Andrew S. C. Yuen, Helga Zoega, Catharina Hartman, Zheng Chang

PMC · DOI: 10.1186/s12916-026-04714-1 · BMC Medicine · 2026-02-20

## TL;DR

People with ADHD are more likely to stop taking antihypertensive medications and have poor adherence, but ADHD medications may help improve adherence.

## Contribution

This multinational study reveals that ADHD is linked to higher antihypertensive medication discontinuation and poor adherence, but ADHD medication use is associated with better adherence.

## Key findings

- ADHD is associated with a 14% higher risk of discontinuing antihypertensive medication over five years.
- ADHD is linked to a 45-64% higher odds of poor adherence to antihypertensive treatment within one to five years.
- Use of ADHD medications is associated with a 42-34% lower odds of poor adherence to antihypertensive treatment among ADHD patients.

## Abstract

Adherence to antihypertensive medication, alongside lifestyle modifications, is fundamental to managing hypertension and reducing the risk of cardiovascular disease. Attention-deficit/hyperactivity disorder (ADHD) is a common neurodevelopmental disorder associated with a range of cardiovascular diseases, including hypertension. ADHD medication has also been associated with hypertension. However, the influence of ADHD and ADHD medication on discontinuation and adherence to antihypertensive treatments is unknown.

We conducted a multinational cohort study using electronic health databases from seven countries, which included adults who initiated antihypertensive medication between 2010 and 2020. ADHD was identified by a diagnosis of ADHD or dispensation of ADHD medications. The outcomes were (1) time to the first discontinuation of antihypertensive medication and (2) poor adherence, defined as the proportion of days covered (PDC) below 80% during 1-, 2-, and 5-year follow-up periods. We used Cox proportional hazards models and logistic regression to estimate associations, adjusting for age, sex, and calendar year of antihypertensive medication initiation. We pooled results from different countries via random-effects meta-analysis.

We identified 12,174,321 adults who initiated antihypertensive medication during the study period, including 320,691 (2.6%) with ADHD. In the pooled analysis across all countries, ADHD was associated with an increased rate of discontinuation in 5-year follow-up of antihypertensive medication (hazard ratio [HR] 1.14; 95% CI, 1.02–1.27). In age-stratified analyses, ADHD was associated with a higher rate of antihypertensive medication discontinuation in middle-aged (HR, 1.11; 95% CI, 1.01–1.23) and older adults (HR, 1.14; 95% CI, 1.01–1.29), but not in young adults. Individuals with ADHD also had higher odds of poor adherence across 1 year after treatment initiation (odds ratio [OR] 1.45, 95% CI 1.26–1.67) to 5 years (OR 1.64, 95% CI 1.34–2.00). Among those with ADHD, use of ADHD medications was associated with lower odds of poor adherence (1 year OR 0.66, 95% CI 0.60–0.73; 5 years OR 0.58, 95% CI 0.46–0.72).

Adults with ADHD are more likely to discontinue antihypertensive treatment and exhibit poor medication adherence. However, ADHD medication use appears to be associated with better adherence among individuals with ADHD.

The online version contains supplementary material available at 10.1186/s12916-026-04714-1.

## Linked entities

- **Diseases:** cardiovascular disease (MONDO:0004995), Attention-deficit/hyperactivity disorder (MONDO:0007743), ADHD (MONDO:0007743)

## Full-text entities

- **Genes:** PDC (phosducin) [NCBI Gene 5132] {aka MEKA, PHD, PhLOP, PhLP}
- **Diseases:** hyperactivity (MESH:D006948), Psychiatric comorbidities (MESH:D001523), Schizophrenia (MESH:D012559), inattention (MESH:D001308), neurodevelopmental disorder (MESH:D002658), impairments in executive functioning (MESH:D003072), impulsivity (MESH:D007174), depression (MESH:D003866), MACE (MESH:D002318), ADHD (MESH:D001289), elevated blood (MESH:D006402), Hypertension (MESH:D006973), death (MESH:D003643), OSF (MESH:D005597)
- **Chemicals:** ACEI (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12930603/full.md

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Source: https://tomesphere.com/paper/PMC12930603