Which medication causes K103N mutation?

Which medication causes K103N mutation?

Multiple studies of EFV administered to treatment-naive patients in combination with tenofovir, stavudine (d4T) or zidovudine (ZDV) and in combination with lamivudine or emtricitabine have shown that the NNRTI resistance mutations – primarily K103N and Y181C –are the most common mutations associated with virological …

What is K103N mutation?

K103N is a non-polymorphic mutation that causes high-level reductions in NVP and EFV susceptibility. 103R. Other. K103R is a polymorphic mutation that alone has no effect on NNRTI susceptibility. However, in combination with V179D, it reduces NVP and EFV susceptibility about 15-fold.

What is M184V mutation?

“M184V” is the shorthand for methionine replacing valine at position 184 in reverse transcriptase. It is by far the most commonly encountered nucleoside reverse transcriptase inhibitor (NRTI) mutation after failure with regimens containing lamivudine (3TC) or emtricitabine (FTC).

What is the signature mutation associated with resistance to emtricitabine and lamivudine?

Most dual–dual NRTI combinations consist of a primary NRTI with lamivudine (3TC) or emtricitabine (FTC) [1,101]. The M184V mutation, conferring high-level resistance to 3TC and FTC, develops rapidly in approximately 50% of treated persons but remains a clinical benefit [2–5].

What is the meaning of NRTI?

Definitions of NRTI. an antiviral drug used against HIV; is incorporated into the DNA of the virus and stops the building process; results in incomplete DNA that cannot create a new virus; often used in combination with other drugs. synonyms: nucleoside reverse transcriptase inhibitor.

Is efavirenz a protease inhibitor?

One group of drugs that efavirenz affects is protease inhibitors, which are used for HIV/AIDS.

What are the most common two pathways of resistance with raltegravir?

Two primary resistance pathways associated with raltegravir treatment failures in the BENCHMRK-1 and BENCHMRK-2 studies have been described, as follows :

  • Q148K/R/H (25-fold decrease in susceptibility)
  • N155H (10-fold decrease in susceptibility)

What is Nnrti?

Non-nucleoside reverse transcriptase inhibitors (NNRTIs) bind to and block HIV reverse transcriptase (an HIV enzyme). HIV uses reverse transcriptase to convert its RNA into DNA (reverse transcription). Blocking reverse transcriptase and reverse transcription prevents HIV from replicating.

Why Lamivudine is called 3tc?

Lamivudine, commonly called 3TC, is an antiretroviral medication used to prevent and treat HIV/AIDS. It is also used to treat chronic hepatitis B when other options are not possible. It is effective against both HIV-1 and HIV-2….Lamivudine.

Clinical data
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CAS Number 134678-17-4
PubChem CID 60825
DrugBank DB00709

What are NRTIs drugs?

Nucleoside reverse transcriptase inhibitors (NRTIs) are active inhibitors of reverse transcriptase found in retroviruses such as the human immunodeficiency virus (HIV). The different nucleoside reverse transcriptase inhibitors may be activated differently but they have the same mechanism of action.

What are the side effects of NRTIs?

NRTIs and Side Effects

  • Nausea.
  • Dizziness.
  • Tiredness.
  • Stomach problems.
  • Headache.
  • Diarrhea.
  • Trouble sleeping.

What class of drug is efavirenz?

Efavirenz is in a class of medications called non-nucleoside reverse transcriptase inhibitors (NNRTIs). It works by decreasing the amount of HIV in the blood.

What is the difference between the k103h and k103t mutations?

K103H is a rare nonpolymorphic mutation that causes high-level resistance (about 20-fold reduced susceptibility) to NVP and EFV ( 41 ). K103T is a rare nonpolymorphic mutation that causes high-level (about 10-fold reduction in susceptibility) resistance to NVP. It has little, if any, effect on EFV susceptibility ( 41, 42, 15 ).

Does the k101r mutation affect NNRTI susceptibility?

K101R is a polymorphic mutation that is not selected by NNRTIs ( 3 ). It has no effect on NNRTI susceptibility ( 10 ). K101N/A/T are nonpolymorphic NNRTI-selected mutations ( 36, 15 ). Their effects on NNRTI susceptibility have not been studied.

What is the difference between K103N and k103s?

K103N is a nonpolymorphic mutation selected in patients receiving NVP and EFV (22,37,38,23). It reduces NVP and EFV susceptibility by about 50 and 20-fold, respectively (13,39,40,14,10). K103S is a nonpolymorphic two base-pair mutation selected by NVP and EFV.

What is the pathophysiology of type k101p?

K101P is a nonpolymorphic two base-pair mutation selected in persons receiving each of the NNRTIs except possibly DOR for which few data are available ( 23, 30, 4 ). It reduces NVP, EFV, and RPV susceptibility by >50-fold and ETR susceptibility by ~5-fold ( 32, 28, 2, 33, 34, 10 ).

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