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Abstract

Objective

Although attention deficit hyperactivity disorder (ADHD) in adults is associated with significant morbidity and dysfunction and afflicts both sexes, relatively few imaging studies have examined female subjects and none have had sufficient power to adequately examine sex differences. The authors examined sex differences in the neural functioning of adults with ADHD during performance of a verbal working memory task.

Method

The participants were 44 adults with ADHD matched on age, sex, and estimated IQ to 49 comparison subjects. Accuracy and reaction time on an N-back task were measured to assess working memory. The blood-oxygen-level-dependent functional MRI response was used as a measure of neural activity.

Results

A group-by-sex analysis of variance showed no between-group differences in either reaction time or percent correct for the working memory task. For both sexes combined, the adults with ADHD showed less activity than comparison subjects in prefrontal regions. However, sex-by-group analyses revealed an interaction, such that male ADHD subjects showed significantly less activity in right frontal, temporal, and subcortical regions and left occipital and cerebellar regions relative to male comparison subjects, whereas female ADHD subjects showed no differences from female comparison subjects. Exploratory correlation analyses revealed negative associations between working-memory-related activation and number of hyperactive symptoms for men and number of inattentive symptoms for women.

Conclusions

Male but not female adults with ADHD showed significantly altered patterns of neural activity during a verbal working memory task. Men and women showed different associations between neural activity and ADHD symptoms.

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Information & Authors

Information

Published In

Go to American Journal of Psychiatry
Go to American Journal of Psychiatry
American Journal of Psychiatry
Pages: 86 - 94
PubMed: 19884224

History

Received: 18 February 2009
Accepted: 20 July 2009
Published online: 1 January 2010
Published in print: January 2010

Authors

Details

Joseph Biederman, M.D.
Stephen V. Faraone, Ph.D.
Nikos Makris, M.D., Ph.D.
Michael C. Monuteaux, Sc.D.
Susan Whitfield-Gabrieli, Ph.D.
Michael Vitulano, B.A.
Michael Schiller, B.A.
Larry J. Seidman, Ph.D.

Notes

Presented in part at the 13th annual meeting of the Organization for Human Brain Mapping, Chicago, June 10–14, 2007; at the 54th annual meeting of the American Academy of Child and Adolescent Psychiatry, Boston, Oct. 23–28, 2007; and at the 15th annual meeting of the Cognitive Neuroscience Society, San Francisco, April 12–15, 2008. Received Feb. 18, 2009; revisions received June 2 and July 16, 2009; accepted July 20, 2009. From the Clinical and Research Programs in Pediatric Psychopharmacology and Adult ADHD and the Psychiatric Neuroscience Division, Massachusetts General Hospital and Harvard Medical School, Charlestown and Boston. Address correspondence to Dr. Valera, Department of Psychiatry, Rm. 2660, Massachusetts General Hospital, 149 13th St., Charlestown, MA 02129; [email protected] (e-mail).

Competing Interests

In the past 12 months, Dr. Valera has received travel support and/or honoraria from divisions of Ortho-McNeil-Janssen Pharmaceuticals, honoraria from Massachusetts General Hospital, Reed Exhibitions, and Boston University, research support from NIH, and reimbursements from Veritas Institute; in the past, she has received travel support from Eli Lilly and Shire, honoraria from Shire, Remedica Medical Education and Publishing, Massachusetts General Hospital, Reed Exhibitions, Boston University, and Partners Healthcare, and research support from NIH. Dr. Biederman is currently receiving research support from Alza, AstraZeneca, Bristol-Myers Squibb, Eli Lilly, Janssen, McNeil, Merck, Organon, Otsuka, Shire, NIMH, and the National Institute of Child Health and Human Development; in 2009 he received speaking fees from the Fundación Ramón Areces, Medice Pharmaceuticals, and the Spanish Child Psychiatry Association; in previous years he received research support, consultation fees, or speaking fees from Abbott, AstraZeneca, Celltech, Cephalon, Eli Lilly, Esai, Forest, Glaxo, Gliatech, Janssen, McNeil, NARSAD, the National Institute on Drug Abuse, New River, Novartis, Noven, Neurosearch, Pfizer, Pharmacia, the Prechter Foundation, Shire, the Stanley Foundation, UCB Pharma, and Wyeth. In the past year, Dr. Faraone has received consulting fees and been on advisory boards for Eli Lilly and Shire and has received research support from Eli Lilly, NIH, Pfizer, and Shire; in previous years, he received consulting fees, was on advisory boards, or was a speaker for Eli Lilly, Janssen, McNeil, Novartis, Pfizer, and Shire and received research support from Eli Lilly, NIH, Pfizer, and Shire. The other authors report no financial relationships with commercial interests.

Funding Information

Supported in part by National Research Service award F32 MH-065040 from NIMH (Dr. Valera); by Clinical Research Training Program Fellowship in Biological and Social Psychiatry MH-16259 from NIMH (Dr. Valera); by NIMH grants MH-57934 (Dr. Faraone), MH-62152 (Dr. Seidman), MH-071535 (Dr. Valera), and MH-084041 (Dr. Makris); by National Center for Research Resources grant P41 RR-14075; by ARRA-NIH-NCCAM grant 1PO1 AT-002048-06 from the National Center for Complementary and Alternative Medicine (Dr. Makris); by a Livingston Fellowship through Harvard Medical School (Dr. Valera); by the National Alliance for Research on Schizophrenia and Depression (Dr. Biederman); by research grants from Janssen and McNeil (Dr. Biederman); by the Research Council for Pediatric Psychopharmacology at the Massachusetts General Hospital; and by the Mental Illness and Neuroscience Discovery (MIND) Institute, March of Dimes Foundation and the Commonwealth Research Center, Massachusetts Department of Mental Health (Dr. Seidman). These funders had no role in the design and conduct of the study; in the collection, management, analysis, and interpretation of the data; or in the preparation, review, and approval of the manuscript.

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