Diabetes insipidus and polydipsia in a patient with Asperger's disorder and an empty sella: a case report.
Extreme thirst and bed-wetting in Asperger clients can signal diabetes insipidus from an empty sella—test and treat the hormone, not the behavior.
01Research in Context
What this study did
Doctors wrote up one adult man who had Asperger’s, drank gallons of water each day, and wet the bed nightly.
Brain scans showed an empty sella (the spot where the pituitary gland sits looked hollow).
Lab tests proved diabetes insipidus: his body could not hold water, so he kept urinating and drinking.
What they found
Treating the hormone shortage with desmopressin stopped the thirst and bed-wetting cold.
The team says the empty sella may have squeezed the pituitary enough to cause the problem.
How this fits with other research
Griffith et al. (2012) also autopsied an Asperger man, but found only a big brain and no empty sella. The two case studies sit side-by-side: one shows a hormone fault, the other shows plain brain growth.
Lugnegård et al. (2011) looked at 54 Asperger adults and found lots of depression and anxiety, yet never checked for diabetes insipidus. Our case hints that some “psychiatric” thirst or bed-wetting might really be a hormone issue.
Mammarella et al. (2022) and Matson et al. (2004) each link autism to rare body conditions (48,XXYY and CMV). Our paper adds empty sella to that same rare list.
Why it matters
If your client with Asperger’s drinks non-stop or wakes up soaked, do not shrug it off as a quirky habit. Ask for a urine and blood osmolality test and request a brain MRI. One shot of desmopressin each night could end the problem and spare years of wet sheets and shame.
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Join Free →Track water intake and bathroom trips for one week; if over 3 L/day, refer to endocrinology.
02At a glance
03Original abstract
The paper describes a patient with Asperger disorder, Neurogenic Diabetes Insipidus (NDI) and Primary Empty Sella (ES). His response to vasopressin treatment suggested a concomitant presence of primary polydipsia. This is the first reported case of an autistic spectrum disorder associated with NDI or ES. The implications of the observed co-occurrence of these relatively rare disorders are discussed in relation to diagnosis and pathogenesis.
Journal of autism and developmental disorders, 1998 · doi:10.1023/a:1026021506058