PMID- 36627777 OWN - NLM STAT- MEDLINE DCOM- 20230619 LR - 20230619 IS - 2212-3873 (Electronic) IS - 1871-5303 (Linking) VI - 23 IP - 8 DP - 2023 TI - Use of Saliva to Assess the Adherence to Treatment with Oral Hypoglycemic Agents in Patients with Type 2 Diabetes. PG - 1068-1076 LID - 10.2174/1871530323666230110123143 [doi] AB - BACKGROUND: The diagnosis of Type 2 Diabetes Mellitus (T2DM) is made by demonstrating the hypoglycemic condition, which involves the determination of plasma glucose, and the follow-up of hypoglycemic treatment is performed by assessing the glycated hemoglobin (HbA1c) concentration. AIM: The aim of this study was to evaluate the saliva as an alternative sample in assessing the adherence to treatment with oral hypoglycemic agents in patients with Type 2 Diabetes. METHODS: We selected 68 patients with T2DM, who were subjected to venous blood and saliva collection, in addition to answering a standardized questionnaire on adherence to hypoglycemic treatment. Laboratory tests performed on saliva, whole blood, serum or plasma included assessment of glycemia, urea, creatinine, uric acid, total cholesterol, HDL-cholesterol, LDL-cholesterol, VLDL-cholesterol, and glycated hemoglobin. RESULTS: It was concluded that 82% of the patients adhered to hypoglycemic treatment based on glycated hemoglobin concentration (cut-off value of 7.0%). Comparing the groups that adhered to hypoglycemic treatment and those that did not adhere, statistical differences (P<0.05) were observed in the glucose, HDL-cholesterol, triglycerides, and insulin use (insulin therapy) parameters. Plasma glucose and urea serum concentration showed positive correlations when compared to saliva samples. Regarding the questionnaire, it was found that 35% of the patients presented positive screening for belief barriers and 83% positive score for recall barriers, and the positive screening correlated with glycated hemoglobin. CONCLUSION: Data have shown that it is possible to use saliva as an alternative sample to the laboratory assessment of hypoglycemic treatment adherence in T2DM patients. CI - Copyright(c) Bentham Science Publishers; For any queries, please email at epub@benthamscience.net. FAU - de Faria Baltazar, Heloisa AU - de Faria Baltazar H AD - Department of Pharmaceutical Science, Universidade Federal de Sao Paulo/UNIFESP, Diadema, Brazil. FAU - Fonseca, Fernando Luiz Affonso AU - Fonseca FLA AD - Department of Pharmaceutical Science, Universidade Federal de Sao Paulo/UNIFESP, Diadema, Brazil. AD - Clinical Analysis Laboratory, Centro Universitario Saude ABC, Santo Andre, Brazil. FAU - Castelo, Paula Midori AU - Castelo PM AD - Department of Pharmaceutical Science, Universidade Federal de Sao Paulo/UNIFESP, Diadema, Brazil. FAU - da Costa Aguiar Alves, Beatriz AU - da Costa Aguiar Alves B AD - Department of Pharmaceutical Science, Universidade Federal de Sao Paulo/UNIFESP, Diadema, Brazil. FAU - Gascon, Thais AU - Gascon T AD - Clinical Analysis Laboratory, Centro Universitario Saude ABC, Santo Andre, Brazil. FAU - da Veiga, Glaucia Luciano AU - da Veiga GL AD - Clinical Analysis Laboratory, Centro Universitario Saude ABC, Santo Andre, Brazil. FAU - Pereira, Edimar Cristiano AU - Pereira EC AD - Department of Pharmaceutical Science, Universidade Federal de Sao Paulo/UNIFESP, Diadema, Brazil. LA - eng PT - Journal Article PL - United Arab Emirates TA - Endocr Metab Immune Disord Drug Targets JT - Endocrine, metabolic & immune disorders drug targets JID - 101269157 RN - 0 (Glycated Hemoglobin) RN - 0 (Blood Glucose) RN - 0 (Hypoglycemic Agents) RN - 0 (Insulin) RN - 0 (Cholesterol, LDL) RN - 8W8T17847W (Urea) SB - IM MH - Humans MH - *Diabetes Mellitus, Type 2/diagnosis/drug therapy MH - Glycated Hemoglobin MH - Blood Glucose MH - Saliva MH - Hypoglycemic Agents MH - Insulin MH - Cholesterol, LDL MH - Urea OTO - NOTNLM OT - Type 2 diabetes mellitus OT - VLDL OT - glycated hemoglobin OT - hypoglycemia OT - pharmacotherapeutic OT - saliva EDAT- 2023/01/12 06:00 MHDA- 2023/06/19 13:08 CRDT- 2023/01/11 00:32 PHST- 2022/06/13 00:00 [received] PHST- 2022/11/03 00:00 [revised] PHST- 2022/11/08 00:00 [accepted] PHST- 2023/06/19 13:08 [medline] PHST- 2023/01/12 06:00 [pubmed] PHST- 2023/01/11 00:32 [entrez] AID - EMIDDT-EPUB-128710 [pii] AID - 10.2174/1871530323666230110123143 [doi] PST - ppublish SO - Endocr Metab Immune Disord Drug Targets. 2023;23(8):1068-1076. doi: 10.2174/1871530323666230110123143.