Monday, April 9, 2018

Blood Test May Distinguish Anorexia From 'Constitutional Thinness

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' NICE, France – A simple, inexpensive blood test can help clinicians to distinguish between anorexia nervosa (AN) and constitutional thinness (CT) in severely underweight young women, new research suggests. Since the introduction of the Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-5), the diagnostic criteria for AN have relied on psychological factors, making it harder to distinguish AN from CT. However, a new study of more than 150 young women showed that blood levels of a thyroid hormone can be used to distinguish the two conditions with high sensitivity and specificity. In cases in which the exclusive use of psychological criteria is not sufficient, the diagnosis of AN "should be completed by at least free T3 determination, which is a cheap and accessible" test, note Natacha Germain, MD, PhD, Endocrinology and Eating Disorders Reference Center, Centre Hospitalier Universitaire de Saint-Étienne, France, and colleagues. The findings were presented here at the European Psychiatric Association (EPA) 2018 Congress. Germain told meeting attendees that using criteria from the DSM-IV to differentiate between AN and CT in a young woman whose body mass index was less than 18.5 kg/m2 was "quite easy." That's because the criteria for AN included the presence of an eating disorder, resistance to food intake, and amenorrhea. In contrast, CT was "a state with no eating disorder, no resistance to body weight gain, no undernutrition, and no amenorrhea." However, the amenorrhea criteria were removed with the introduction of the DSM-5, making it easier to confuse AN and CT. This confusion "is highly detrimental, especially for CT, because of the social stigmatization, health insurance penalty, and the inefficient, aggressive therapy applied in this population," said Germain. To identify distinguishing markers that could be used to easily tell the difference between the two conditions, the investigators studied 40 patients with AN, 56 patients with CT, and 54 women with normal weight, who served as controls. DSM-IV criteria were used to define AN and CT. They evaluated hormonal and nutritional parameters, and administered a series of psychiatric questionnaires to find robust, distinguishing markers that would fit with criteria from the DSM-5. Performing receiver operating characteristic curve analysis, they found that only the restrained eating subscale of the Dutch Eating Behavior Questionnaire could be used to distinguish between AN and CT. It had a specificity of 94% and a sensitivity of 95% at a cutoff of 0.74. "Unfortunately, it's only one dimension in a complex questionnaire, and it's sometimes biased by denial," said Germain. She added that in clinical practice, the availability of the questionnaire is very low. Estradiol was, as expected, the best marker for distinguishing between the two populations. It had a sensitivity and specificity of 87% and 80%, respectively, at a cutoff of 24. However, using estradiol as a biomarker in this context is incompatible with the DSM-5, Germain noted. Leptin was also very good at distinguishing between the conditions, with a specificity of 80% and a sensitivity of 84% at a cutoff of 2.58. "Unfortunately, leptin testing has a low availability and high cost, so it's not very easy to use it as a marker," she said. The researchers found that free triiodothyronine (T3) levels could be used to distinguish between the patient groups It had a sensitivity of 80% and a specificity of 91% at a cut-off of 3.3 pmol/L (P < .0001). Moreover, the test for free T3 levels is cheap, and the results are simple to interpret. It is also widely available. Germain concluded that for a young, thin woman, a free T3 level of less than 3.3 pmol/L indicates AN with undernutrition. Psychiatric Association (EPA) 2018 Congress. Abstract OR0174, presented March 6, 2018. Read more details from this article: Blood Test May Distinguish Anorexia From 'Constitutional Thinness' - Medscape - Mar 07, 2018. https://www.medscape.com/viewarticle/893578#vp_1

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