Reconsidering the Age-of-Onset Criterion in Older Adults Being Evaluated for ADHD
The current Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-5) requires evidence of symptom onset before age 12 to make a diagnosis of ADHD in adults.
A recently published clinical review questions the appropriateness of this criterion in older adults 50 years old and above. It sets forth several reasons:
ADHD was first recognized in the DSM in 1968, just over fifty years ago. Anyone over fifty is highly unlikely to have been diagnosed with ADHD in childhood, or even to have symptoms properly noticed.
It is well-established that memories both fade and change with time. Even among young adults, only about half can recall the age at which specific memories occurred. For older adults, the challenge is much greater, and that means questionnaire answers become unreliable.
Episodic memory among persons with ADHD is known to be impaired relative to controls, which further limits the reliability of memory, especially over extended periods.
On the other hand, the reason for the early onset criterion is to avoid any confusion with early neurodegenerative diseases such as Alzheimer's or Lewy body dementia, which have overlapping symptoms.
The authors suggest a possible fix:
For those over fifty, readjust the under-12 criterion to instead demonstrate the longstanding previous existence of ADHD symptoms, without forcing it to include the first eleven years of life. They call for research to determine how many years of previous symptoms would best distinguish ADHD symptoms from normal aging and the onset of dementia.
Establish a family history of ADHD. Heritability estimates suggest that ADHD occurs in roughly half the parents of people with ADHD, and about 15% of grandparents. That means that for persons over 50, having children and/or grandchildren with ADHD would lend greater weight to self-reported ADHD symptoms.
Noting that "cognitive functioning rating scales(e.g., the Barkley Deficits in Executive Functioning Scale) have shown to align robustly with ADHD symptoms," they "call for studies investigating the use of these rating scales in older adult samples, and particularly their discriminant validity relative to other late-life disorders affecting cognition."
This would be accompanied by careful screening for physical or psychiatric comorbidities, to reduce the risk of false positives.
It is unethical, the authors suggest, to deny care to older, presently undiagnosed adults, given the demonstrated poor outcomes associated with untreated ADHD.
Manu J. Sharma, Sasha Lavoie, Brandy L. Callahan, "A Call for Research on the Validity of the Age-of-Onset Criterion Application in OlderAdults Being Evaluated for ADHD: A Review of the Literature in Clinical andCognitive Psychology," American Journal of Geriatric Psychiatry (2020),https://doi.org/10.1016/j.jagp.2020.10.016.
ADHD (Attention-Deficit/Hyperactivity Disorder) is one of the most studied neurodevelopmental conditions, with many clinical trials evaluating the effectiveness and safety of various medications. These trials, known as randomized controlled trials (RCTs), are considered the gold standard for assessing treatments. However, strict eligibility criteria often exclude many real-world patients, raising questions about whether the findings from these trials apply to everyday clinical settings.
Our latest study sheds light on this issue, revealing just how many individuals with ADHD might be excluded from RCTs and the impact this exclusion has on their treatment outcomes.
Method
Researchers used Swedish national registries to analyze data from 189,699 individuals diagnosed with ADHD who started medication between 2007 and 2019. They applied exclusion criteria from 164 international RCTs to identify who would have been considered ineligible for these trials in order to determine the proportion of individuals with ADHD who would not meet the eligibility criteria for RCTs.
Key Findings
Many Patients Are Ineligible for Clinical Trials:
Over half (53%) of the study population would have been ineligible for ADHD medication trials.
Adults were most likely to be excluded (74%), followed by adolescents (35%) and children (21%).
Ineligible Patients Face Unique Challenges:
Treatment Switching: Ineligible individuals were more likely to switch medications within the first year (14% higher likelihood compared to eligible patients).
Medication Discontinuation: They were slightly less likely to stop taking their medication during the first year.
Higher Risk of Adverse Outcomes:
Ineligible patients experienced significantly higher rates of psychiatric hospitalizations and health issues such as depression, anxiety, and substance use disorders. For instance:some text
Psychiatric hospitalizations: Nearly 10 times more likely.
Specialist visits for substance use disorders: About 15 times more likely.
Anxiety-related visits: Over 11 times more likely.
What This Means
These findings highlight a major gap between the controlled environments of clinical trials and the realities faced by individuals with ADHD in everyday life. While RCTs provide valuable insights, their restrictive criteria often exclude patients with more complex health profiles or co-existing conditions. This limits the generalisability of trial results, meaning that treatment guidelines based solely on RCTs may not fully address the needs of all patients.
Conclusion
This study demonstrated that a significant proportion of individuals with ADHD, particularly adults, do not meet the eligibility criteria for standard RCTs. These results emphasize the importance of bridging the gap between research settings and real-world applications. By recognizing and addressing the limitations of RCTs, we can work towards more equitable and effective ADHD treatment strategies for everyone.
Our understanding of Attention-deficit/hyperactivity disorder (ADHD) has grown and evolved considerably since it first appeared in the DSM-II as “Hyperkinetic Reaction of Childhood.” This study aimed to find the disorder’s placement within the modern psychopathology classification systems like the Hierarchical Taxonomy Of Psychopathology (HiTOP).
The HiTOP model aims to address limitations of traditional classification systems for mental illness, such as the DSM-5 and ICD-10, by organizing psychopathology according to evidence from research on observable patterns of mental health problems.. Is ADHD best categorized under externalizing conditions, neurodevelopmental disorders, or something else entirely? A recent study by Zheyue Peng, Kasey Stanton, Beatriz Dominguez-Alvarez, and Ashley L. Watts takes a closer look at this question using a symptom-focused approach.
The Study:
Traditionally, ADHD has been associated with externalizing behaviors, such as impulsivity and hyperactivity, or with neurodevelopmental traits, like cognitive delays. However, this study challenges the idea of placing ADHD into a single category. Instead, it maps ADHD symptoms across three major psychopathology spectra: externalizing, neurodevelopmental, and internalizing.
The findings reveal that ADHD symptoms don’t fit neatly into one box. For example, symptoms like impulsivity, poor school performance, and low perseverance were strongly associated with externalizing behaviors. On the other hand, cognitive disengagement (e.g., daydreaming, blank staring) and immaturity were closely linked to neurodevelopmental challenges. Interestingly, cognitive disengagement also showed ties to internalizing symptoms, such as anxiety or depression.
This research underscores the complexity of ADHD. Rather than treating ADHD as a single, unitary construct, the study advocates for a symptom-based approach to better understand and treat individuals. By acknowledging that ADHD symptoms relate to multiple psychopathology spectra, clinicians and researchers can move toward more nuanced classification systems and targeted interventions.
Conclusion:
Ultimately, this study highlights the need for modern systems to move beyond rigid categories and adopt a more flexible, symptom-focused framework for understanding ADHD’s place in psychopathology.
Exposure to heavy metals like lead, arsenic, mercury, cadmium, and manganese is known to harm developing nervous systems. However, past studies on whether heavy metals specifically increase the risk of ADHD have shown mixed results.
A research team from China (Gu et al., 2024) reviewed medical studies and conducted meta-analyses to better understand this issue.
Methods:
The team included studies on children and teens, focusing on cohort studies, case-control studies, and cross-sectional studies. They only used articles written in English and required validated biomonitoring (like blood tests) to measure heavy metal exposure. ADHD diagnoses had to come from clinical evaluations.
To be included, studies had to report effect sizes such as odds ratios and relative risks with confidence intervals. The team focused on comparisons between groups with high, low, or no exposure, which made it harder to analyze dose-response relationships.
They also evaluated the quality of each study. All cohort studies were rated high-quality. Of the 15 case-control studies, 6 were high-quality, and 9 were moderate-quality. Among cross-sectional studies, only 2 were high-quality, and the rest were moderate-quality.
Key Findings:
Lead Exposure and ADHD:some text
A meta-analysis of 22 studies with over 20,000 participants found that early exposure to lead was linked to about twice the odds of an ADHD diagnosis compared to unexposed children.
However, results varied widely among studies, and signs of publication bias were detected. After adjusting for this bias, the increased odds dropped to about 50%.
A dose-response relationship was found:some text
Blood lead levels of 2.5 µg/dL increased ADHD risk by 1.8 times.
Levels of 5 µg/dL increased the risk 2.5 times.
Levels of 7.5 µg/dL increased the risk 2.75 times.
Levels of 10 µg/dL tripled the risk.
Other Metals:some text
No significant links were found between ADHD and exposure to arsenic, mercury, cadmium, or manganese. Fewer studies were available for these metals, and participant numbers were much smaller:some text
Austrian Study: An Austrian team (Rosenauer et al., 2024) also conducted a meta-analysis on lead exposure and ADHD. They included 14 studies with over 7,600 participants and found:some text
Lead exposure increased the odds of ADHD by about 25%.
Studies focusing on higher lead levels found a 43% increased risk, supporting a dose-response relationship.
Study results were consistent, with no signs of publication bias.
Conclusion:
There was no evidence linking ADHD to other heavy metals like arsenic, mercury, cadmium, or manganese. Both meta-analyses suggest that lead exposure is associated with the risk for ADHD. However, because these studies cannot rule out other explanations, one cannot conclude that lead exposure causes ADHD. For example, other work shows that people with ADHD are likely to have lower incomes than those without ADHD.