Page last updated: 2024-10-18

formaldehyde and Diabetes Mellitus

formaldehyde has been researched along with Diabetes Mellitus in 17 studies

paraform: polymerized formaldehyde; RN given refers to parent cpd; used in root canal therapy

Diabetes Mellitus: A heterogeneous group of disorders characterized by HYPERGLYCEMIA and GLUCOSE INTOLERANCE.

Research Excerpts

ExcerptRelevanceReference
"Formaldehyde may cause cytotoxicity, which induces vascular endothelial injury and mediates multiple factor-induced pathogenic process of vascular injury."2.46[Endogenous formaldehyde and cardiovascular diseases]. ( Du, JB; Tang, CS; Zhang, FW, 2010)
"The complications of diabetic polyneuropathy (DN) determines its level of severity."1.56Expressions of spinal microglia activation, BDNF, and DREAM proteins correlated with formalin-induced nociceptive responses in painful and painless diabetic neuropathy rats. ( Ab Aziz, CB; Ismail, CAN; Long, I; Suppian, R, 2020)
"Methylamine was observed to be deaminated by several semicarbazide-sensitive amine oxidases, which were prepared from blood and vascular tissues of various species, including humans."1.29Oxidative deamination of methylamine by semicarbazide-sensitive amine oxidase leads to cytotoxic damage in endothelial cells. Possible consequences for diabetes. ( Yu, PH; Zuo, DM, 1993)

Research

Studies (17)

TimeframeStudies, this research(%)All Research%
pre-19904 (23.53)18.7374
1990's4 (23.53)18.2507
2000's0 (0.00)29.6817
2010's5 (29.41)24.3611
2020's4 (23.53)2.80

Authors

AuthorsStudies
Ismail, CAN2
Ghazali, AK1
Suppian, R2
Abd Aziz, CB1
Long, I2
Zhu, BT1
Ab Aziz, CB1
Xu, H1
Liu, Q1
Song, X1
Wang, C1
Wang, X3
Ma, S1
Feng, Y1
Meng, X1
Liu, X1
Wang, W1
Lou, K1
Gao, ZF1
Ogbe, AY1
Sann, EE1
Xia, F1
Orru, H1
Idavain, J1
Pindus, M1
Orru, K1
Kesanurm, K1
Lang, A1
Tomasova, J1
Winiczenko, R1
Górnicki, K1
Kaleta, A1
Janaszek-Mańkowska, M1
Khan, ZA1
Singh, C1
Khan, T1
Ganguly, M1
Bradsher, C1
Goodwin, P1
Petty, JT1
Sandau, C1
Bove, DG1
Marsaa, K1
Bekkelund, CS1
Lindholm, MG1
Salazar, J1
Bermúdez, V1
Olivar, LC1
Torres, W1
Palmar, J1
Añez, R1
Ordoñez, MG1
Rivas, JR1
Martínez, MS1
Hernández, JD1
Graterol, M1
Rojas, J1
Mubarak, Z1
Humaira, A1
Gani, BA1
Muchlisin, ZA1
Gremillet, C1
Jakobsson, JG1
Gomila, A1
Shaw, E1
Carratalà, J1
Leibovici, L1
Tebé, C1
Wiegand, I1
Vallejo-Torres, L1
Vigo, JM1
Morris, S1
Stoddart, M1
Grier, S1
Vank, C1
Cuperus, N1
Van den Heuvel, L1
Eliakim-Raz, N1
Vuong, C1
MacGowan, A1
Addy, I1
Pujol, M1
Cobb, A1
Rieger, E1
Bell, J1
Mallik, S1
Zhao, Z1
Szécsényi, Á1
Li, G1
Gascon, J1
Pidko, EA1
Zhang, GR1
Wolker, T1
Sandbeck, DJS1
Munoz, M1
Mayrhofer, KJJ1
Cherevko, S1
Etzold, BJM1
Lukashuk, L1
Yigit, N1
Rameshan, R1
Kolar, E1
Teschner, D1
Hävecker, M1
Knop-Gericke, A1
Schlögl, R1
Föttinger, K1
Rupprechter, G1
Franconieri, F1
Deshayes, S1
de Boysson, H1
Trad, S1
Martin Silva, N1
Terrier, B1
Bienvenu, B1
Galateau-Sallé, F1
Emile, JF1
Johnson, AC1
Aouba, A1
Vogt, TJ1
Gevensleben, H1
Dietrich, J1
Kristiansen, G1
Bootz, F1
Landsberg, J1
Goltz, D1
Dietrich, D1
Idorn, M1
Skadborg, SK1
Kellermann, L1
Halldórsdóttir, HR1
Holmen Olofsson, G1
Met, Ö1
Thor Straten, P1
Johnson, LE1
Brockstedt, D1
Leong, M1
Lauer, P1
Theisen, E1
Sauer, JD1
McNeel, DG1
Morandi, F1
Marimpietri, D1
Horenstein, AL1
Bolzoni, M1
Toscani, D1
Costa, F1
Castella, B1
Faini, AC1
Massaia, M1
Pistoia, V1
Giuliani, N1
Malavasi, F1
Qiu, J1
Peng, S1
Yang, A1
Ma, Y1
Han, L1
Cheng, MA1
Farmer, E1
Hung, CF1
Wu, TC1
Modak, S1
Le Luduec, JB1
Cheung, IY1
Goldman, DA1
Ostrovnaya, I1
Doubrovina, E1
Basu, E1
Kushner, BH1
Kramer, K1
Roberts, SS1
O'Reilly, RJ1
Cheung, NV1
Hsu, KC1
Salgarello, T1
Giudiceandrea, A1
Calandriello, L1
Marangoni, D1
Colotto, A1
Caporossi, A1
Falsini, B1
Lefrançois, P1
Xie, P1
Wang, L2
Tetzlaff, MT1
Moreau, L1
Watters, AK1
Netchiporouk, E1
Provost, N1
Gilbert, M1
Ni, X1
Sasseville, D1
Wheeler, DA1
Duvic, M1
Litvinov, IV1
O'Connor, BJ1
Fryda, NJ1
Ranglack, DH1
Yang, Y2
Yang, J1
Zhang, X2
Grün, AL1
Emmerling, C1
Aumeeruddy-Elalfi, Z1
Ismaël, IS1
Hosenally, M1
Zengin, G1
Mahomoodally, MF1
Dotsenko, A1
Gusakov, A1
Rozhkova, A1
Sinitsyna, O1
Shashkov, I1
Sinitsyn, A1
Hong, CE1
Kim, JU1
Lee, JW1
Lee, SW1
Jo, IH1
Pandiyarajan, S1
Premasudha, P1
Kadirvelu, K1
Wang, B1
Luo, L1
Wang, D1
Ding, R1
Hong, J1
Caviezel, D1
Maissen, S1
Niess, JH1
Kiss, C1
Hruz, P1
Pockes, S1
Wifling, D1
Keller, M1
Buschauer, A1
Elz, S1
Santos, AF1
Ferreira, IP1
Pinheiro, CB1
Santos, VG1
Lopes, MTP1
Teixeira, LR1
Rocha, WR1
Rodrigues, GLS1
Beraldo, H1
Lohar, S1
Dhara, K1
Roy, P1
Sinha Babu, SP1
Chattopadhyay, P1
Sukwong, P1
Sunwoo, IY1
Lee, MJ1
Ra, CH1
Jeong, GT1
Kim, SK2
Huvinen, E1
Eriksson, JG1
Stach-Lempinen, B1
Tiitinen, A1
Koivusalo, SB1
Malhotra, M1
Suresh, S1
Garg, A1
Wei, L1
Jiang, Y2
Zhou, W1
Liu, S1
Liu, Y1
Rausch-Fan, X1
Liu, Z1
Marques, WL1
van der Woude, LN1
Luttik, MAH1
van den Broek, M1
Nijenhuis, JM1
Pronk, JT1
van Maris, AJA1
Mans, R1
Gombert, AK1
Xu, A1
Sun, J1
Li, J1
Chen, W2
Zheng, R1
Han, Z1
Ji, L1
Shen, WQ1
Bao, LP1
Hu, SF1
Gao, XJ1
Xie, YP1
Gao, XF1
Huang, WH1
Lu, X1
Gostin, PF1
Addison, O1
Morrell, AP1
Zhang, Y2
Cook, AJMC1
Liens, A1
Stoica, M1
Ignatyev, K1
Street, SR1
Wu, J1
Chiu, YL1
Davenport, AJ1
Qiu, Z1
Shu, J1
Tang, D1
Gao, X1
Zhang, J3
Huang, K1
Wai, H1
Du, K1
Anesini, J1
Kim, WS1
Eastman, A1
Micalizio, GC1
Liang, JH1
Huo, XK1
Cheng, ZB1
Sun, CP1
Zhao, JC1
Kang, XH1
Zhang, TY1
Chen, ZJ1
Yang, TM1
Wu, YY1
Deng, XP1
Zhang, YX1
Salem, HF1
Kharshoum, RM1
Abou-Taleb, HA1
AbouTaleb, HA1
AbouElhassan, KM1
Ohata, C1
Ohyama, B1
Kuwahara, F1
Katayama, E1
Nakama, T1
Kobayashi, S1
Kashiwagi, T1
Kimura, J1
Lin, JD1
Liou, MJ1
Hsu, HL1
Leong, KK1
Chen, YT1
Wang, YR1
Hung, WS1
Lee, HY1
Tsai, HJ1
Tseng, CP1
Alten, B1
Yesiltepe, M1
Bayraktar, E1
Tas, ST1
Gocmen, AY1
Kursungoz, C1
Martinez, A1
Sara, Y1
Huang, S2
Adams, E1
Van Schepdael, A1
Wang, Q1
Chung, CY1
Yang, W1
Yang, G1
Chough, S1
Chen, Y1
Yin, B1
Bhattacharya, R1
Hu, Y1
Saeui, CT1
Yarema, KJ1
Betenbaugh, MJ1
Zhang, H1
Patik, JC1
Tucker, WJ1
Curtis, BM1
Nelson, MD1
Nasirian, A1
Park, S1
Brothers, RM1
Dohlmann, TL1
Hindsø, M1
Dela, F1
Helge, JW1
Larsen, S1
Gayani, B1
Dilhari, A1
Wijesinghe, GK1
Kumarage, S1
Abayaweera, G1
Samarakoon, SR1
Perera, IC1
Kottegoda, N1
Weerasekera, MM1
Nardi, MV1
Timpel, M1
Ligorio, G1
Zorn Morales, N1
Chiappini, A1
Toccoli, T1
Verucchi, R1
Ceccato, R1
Pasquali, L1
List-Kratochvil, EJW1
Quaranta, A1
Dirè, S1
Heo, K1
Jo, SH1
Shim, J1
Kang, DH1
Kim, JH1
Park, JH1
Akhtar, N1
Saha, A1
Kumar, V1
Pradhan, N1
Panda, S1
Morla, S1
Kumar, S1
Manna, D1
Wang, H1
Xu, E1
Yu, S1
Li, D1
Quan, J1
Xu, L1
Saslow, SA1
Um, W1
Pearce, CI1
Bowden, ME1
Engelhard, MH1
Lukens, WL1
Kim, DS1
Schweiger, MJ1
Kruger, AA1
Adair, LS1
Kuzawa, C1
McDade, T1
Carba, DB1
Borja, JB1
Liang, X2
Song, W1
Wang, K1
Zhang, B1
Peele, ME1
Luo, HR1
Chen, ZY1
Fei, JJ1
Du, ZJ1
Yi, KJ1
Im, WT1
Kim, DW1
Ji, X1
Zhang, C1
Xu, Z1
Ding, Y1
Song, Q1
Li, B2
Zhao, H1
Lee, DW1
Lee, H1
Kwon, BO1
Khim, JS1
Yim, UH1
Park, H1
Park, B1
Choi, IG1
Kim, BS1
Kim, JJ1
Wang, JJ1
Chen, Q1
Li, YZ1
Sakai, M1
Yamaguchi, M1
Nagao, Y1
Kawachi, N1
Kikuchi, M1
Torikai, K1
Kamiya, T1
Takeda, S1
Watanabe, S1
Takahashi, T1
Arakawa, K1
Nakano, T1
Rufo, S1
Continentino, MA1
Nikolaou, V1
Plass, F1
Planchat, A1
Charisiadis, A1
Charalambidis, G1
Angaridis, PA1
Kahnt, A1
Odobel, F1
Coutsolelos, AG1
Fuentes, I1
García-Mendiola, T1
Sato, S1
Pita, M1
Nakamura, H1
Lorenzo, E1
Teixidor, F1
Marques, F1
Viñas, C1
Liu, F1
Qi, P1
Zhang, L1
Zhang, FW1
Du, JB1
Tang, CS1
Dai, M1
Maxwell, S1
Vogt, BD1
La Belle, JT1
BERARDINELLI, W1
Gallop, PM1
Flückiger, R1
Hanneken, A1
Mininsohn, MM1
Gabbay, KH1
Nishiyama, RH1
Torretti, B1
Martin, DB1
Pek, SB1
Keren, DF1
Yu, PH1
Zuo, DM1
Hunt, JV1
Bottoms, MA1
Mitchinson, MJ1
Takeshita, N1
Yamaguchi, I1
Grönvall, JL1
Garpenstrand, H1
Oreland, L1
Ekblom, J1
Katsilambros, L1

Reviews

1 review available for formaldehyde and Diabetes Mellitus

ArticleYear
[Endogenous formaldehyde and cardiovascular diseases].
    Sheng li ke xue jin zhan [Progress in physiology], 2010, Volume: 41, Issue:1

    Topics: Amine Oxidase (Copper-Containing); Animals; Atherosclerosis; Catalysis; Deamination; Diabetes Mellit

2010

Trials

1 trial available for formaldehyde and Diabetes Mellitus

ArticleYear
    Neural computing & applications, 2018, Volume: 30, Issue:6

    Topics: Activities of Daily Living; Acute Disease; Adalimumab; Adaptation, Physiological; Adenosine Triphosp

2018

Other Studies

15 other studies available for formaldehyde and Diabetes Mellitus

ArticleYear
Lower Formalin-Induced Pain Responses in Painless Diabetic Neuropathy Rat Correlate with the Reduced Spinal Cord NR2B Subunit of N-Methyl-D-Aspartate Receptor Activation.
    Journal of molecular neuroscience : MN, 2022, Volume: 72, Issue:3

    Topics: Animals; Diabetes Mellitus; Diabetic Neuropathies; Formaldehyde; Male; Pain; Rats; Rats, Sprague-Daw

2022
Biochemical mechanism underlying the pathogenesis of diabetic retinopathy and other diabetic complications in humans: the methanol-formaldehyde-formic acid hypothesis.
    Acta biochimica et biophysica Sinica, 2022, Apr-25, Volume: 54, Issue:4

    Topics: Animals; Carbon; Diabetes Mellitus; Diabetic Retinopathy; Formaldehyde; Formates; Glucose; Humans; M

2022
Expressions of spinal microglia activation, BDNF, and DREAM proteins correlated with formalin-induced nociceptive responses in painful and painless diabetic neuropathy rats.
    Neuropeptides, 2020, Volume: 79

    Topics: Animals; Brain-Derived Neurotrophic Factor; Diabetes Mellitus; Diabetic Neuropathies; Formaldehyde;

2020
Fluorophore-Promoted Facile Deprotonation and Exocyclic Five-Membered Ring Cyclization for Selective and Dynamic Tracking of Labile Glyoxals.
    Analytical chemistry, 2020, 10-20, Volume: 92, Issue:20

    Topics: Animals; Arginine; Chromatography, High Pressure Liquid; Cyclization; Diabetes Mellitus; Diabetes Me

2020
Turn-on fluorescent sensor for the detection of glucose using manganese dioxide-phenol formaldehyde resin nanocomposite.
    Talanta, 2018, Apr-01, Volume: 180

    Topics: Biosensing Techniques; Blood Glucose; Diabetes Mellitus; Fluorescent Dyes; Formaldehyde; Humans; Hyd

2018
Residents' Self-Reported Health Effects and Annoyance in Relation to Air Pollution Exposure in an Industrial Area in Eastern-Estonia.
    International journal of environmental research and public health, 2018, 02-02, Volume: 15, Issue:2

    Topics: Adolescent; Adult; Aged; Air Pollutants; Air Pollution; Benzene; Cardiovascular Diseases; Cresols; D

2018
Mesoporous carbon amperometric glucose sensors using inexpensive, commercial methacrylate-based binders.
    Analytica chimica acta, 2012, Aug-13, Volume: 738

    Topics: Animals; Biosensing Techniques; Blood Glucose; Carbon; Diabetes Mellitus; Electrochemical Techniques

2012
[Diabetogenic action of formaldehyde].
    Revista brasileira de medicina, 1955, Volume: 12, Issue:1

    Topics: Diabetes Mellitus; Formaldehyde; Humans

1955
Chemical quantitation of hemoglobin glycosylation: fluorometric detection of formaldehyde released upon periodate oxidation of glycoglobin.
    Analytical biochemistry, 1981, Nov-01, Volume: 117, Issue:2

    Topics: Ammonia; Colorimetry; Diabetes Mellitus; Formaldehyde; Glycated Hemoglobin; Humans; Oxidation-Reduct

1981
The detection of islet-cell antibodies by immunofluorescence in Bouin's-fixed, paraffin-embedded human pancreas.
    Laboratory investigation; a journal of technical methods and pathology, 1980, Volume: 43, Issue:2

    Topics: Acetates; Acetic Acid; Antibodies; Cytological Techniques; Diabetes Mellitus; Fixatives; Fluorescent

1980
Oxidative deamination of methylamine by semicarbazide-sensitive amine oxidase leads to cytotoxic damage in endothelial cells. Possible consequences for diabetes.
    Diabetes, 1993, Volume: 42, Issue:4

    Topics: Amine Oxidase (Copper-Containing); Animals; Benzylamines; Cell Line; Cell Survival; Cells, Cultured;

1993
Oxidative alterations in the experimental glycation model of diabetes mellitus are due to protein-glucose adduct oxidation. Some fundamental differences in proposed mechanisms of glucose oxidation and oxidant production.
    The Biochemical journal, 1993, Apr-15, Volume: 291 ( Pt 2)

    Topics: Benzoates; Benzoic Acid; Cholesterol Esters; Copper; Diabetes Mellitus; Edetic Acid; Electrophoresis

1993
Antinociceptive effects of morphine were different between experimental and genetic diabetes.
    Pharmacology, biochemistry, and behavior, 1998, Volume: 60, Issue:4

    Topics: Analgesics, Opioid; Animals; Diabetes Mellitus; Diabetes Mellitus, Experimental; Dopamine Agents; Do

1998
Autoradiographic imaging of formaldehyde adducts in mice: possible relevance for vascular damage in diabetes.
    Life sciences, 1998, Volume: 63, Issue:9

    Topics: Amine Oxidase (Copper-Containing); Animals; Autoradiography; Deamination; Diabetes Mellitus; Enzyme

1998
Clinical and experimental observations on formalized insulin.
    Israel journal of medical sciences, 1972, Volume: 8, Issue:6

    Topics: Animals; Biological Assay; Diabetes Mellitus; Drug Synergism; Formaldehyde; Guinea Pigs; Humans; Ins

1972