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. 2018 Sep 21;12:652. doi: 10.3389/fnins.2018.00652

Table 2B.

Empirical evidence knowledge score distribution of FMR1 gene mutations in a cohort of PCPs and medical students in Serbia.

Cohort PCPs Medical students
N (%) N (%) P-values
Question 1-5: Are you aware of…
Answers: Yes or No
1. …the availability of an early, precise genetic/medical diagnosis of FMR1 gene FM and/or PM?
Yes 76 (26.8) 147 (60)
No 208 (73.2) 98 (40) P < 0.001*
2. …the professional organizations' recommendation on FMR1 testing in individuals diagnosed with neurodevelopmental and neurodegenerative disorders?
Yes 66 (23.2) 91 (37.1)
No 218 (76.8) 154 (62.9) P < 0.001*
3. …advanced phases clinical trials aimed to “translate” new targeted treatments drugs in clinical practice that could modify core problems in FXS related to autism spectrum disorder?
Yes 39 (13.7) 43 (17.6)
No 245 (86.3) 202 (84.2) P = 0.226
4. … the FXS leading the way in clinical trials among all other developmental disorders, including ASD?
Yes 23 (8.1) 74 (30.2)
No 261 (91.9) 204 (83.3) P = 0.002
5. …0.17 out of 22of these clinical trials aimed to develop targeted drugs focused on the excitatory-inhibitory imbalance in FXS, namely, the mGluR/GABA leading to the excess protein accumulation at dendrite synapses as the hallmark of FXS?
Yes 23 (8.1) 32 (13.1)
No 261 (91.9) 213 (86.9) P = 0.062

FMR1, gene-Fragile X Mental Retardation 1 gene; PCPs, primary care physicians; FM, full mutations; PM, premutation; ASD, Autism Spectrum Disorder; FXS, fragile X syndrome; mGluR, metabotropic glutamate receptor; GABA, gamma, aminobutyric acid.

N, number of the study participants; P values, probability of the data arising by chance;

*

statistically significant data.